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You searched for subject:(N alkylation). Showing records 1 – 30 of 36 total matches.

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Université de Neuchâtel

1. Kholod Zaitseva, Inga. New approaches for the synthesis of advanced precursors of Rhazinilam analogues.

Degree: 2014, Université de Neuchâtel

 The purpose of this thesis was to explore different approaches for the synthesis of advanced precursors of rhazinilam analogues. The intramolecular Michael Addition was envisaged… (more)

Subjects/Keywords: N-alkylation

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APA (6th Edition):

Kholod Zaitseva, I. (2014). New approaches for the synthesis of advanced precursors of Rhazinilam analogues. (Thesis). Université de Neuchâtel. Retrieved from http://doc.rero.ch/record/288671

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kholod Zaitseva, Inga. “New approaches for the synthesis of advanced precursors of Rhazinilam analogues.” 2014. Thesis, Université de Neuchâtel. Accessed April 16, 2021. http://doc.rero.ch/record/288671.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kholod Zaitseva, Inga. “New approaches for the synthesis of advanced precursors of Rhazinilam analogues.” 2014. Web. 16 Apr 2021.

Vancouver:

Kholod Zaitseva I. New approaches for the synthesis of advanced precursors of Rhazinilam analogues. [Internet] [Thesis]. Université de Neuchâtel; 2014. [cited 2021 Apr 16]. Available from: http://doc.rero.ch/record/288671.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kholod Zaitseva I. New approaches for the synthesis of advanced precursors of Rhazinilam analogues. [Thesis]. Université de Neuchâtel; 2014. Available from: http://doc.rero.ch/record/288671

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


King Abdullah University of Science and Technology

2. Alobaid, Nasser A. N-alkylation of amines via dehydrogenative coupling with alcohol catalyzed by the well-defined PN3 rhenium pincer complex.

Degree: Physical Science and Engineering (PSE) Division, 2020, King Abdullah University of Science and Technology

 Transition metals are known to be the essential part in most of the catalysts, the heterogeneous and the homogenous catalysts; however, the ligands that attached… (more)

Subjects/Keywords: N-alkylation; Hydrogenation; Dehydrogenation; Coupling; Pincer; Rhenium

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APA (6th Edition):

Alobaid, N. A. (2020). N-alkylation of amines via dehydrogenative coupling with alcohol catalyzed by the well-defined PN3 rhenium pincer complex. (Thesis). King Abdullah University of Science and Technology. Retrieved from http://hdl.handle.net/10754/662703

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Alobaid, Nasser A. “N-alkylation of amines via dehydrogenative coupling with alcohol catalyzed by the well-defined PN3 rhenium pincer complex.” 2020. Thesis, King Abdullah University of Science and Technology. Accessed April 16, 2021. http://hdl.handle.net/10754/662703.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Alobaid, Nasser A. “N-alkylation of amines via dehydrogenative coupling with alcohol catalyzed by the well-defined PN3 rhenium pincer complex.” 2020. Web. 16 Apr 2021.

Vancouver:

Alobaid NA. N-alkylation of amines via dehydrogenative coupling with alcohol catalyzed by the well-defined PN3 rhenium pincer complex. [Internet] [Thesis]. King Abdullah University of Science and Technology; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10754/662703.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Alobaid NA. N-alkylation of amines via dehydrogenative coupling with alcohol catalyzed by the well-defined PN3 rhenium pincer complex. [Thesis]. King Abdullah University of Science and Technology; 2020. Available from: http://hdl.handle.net/10754/662703

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université Montpellier II

3. Larrouy, Manuel. Nouvelles synthèses totales de la nicotianamines et d'analogues : New strategies for total synthesis of nicotianamine and analogues.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2010, Université Montpellier II

Nos travaux ont porté sur la mise au point de nouvelles stratégies de synthèse de la nicotianamine (molécule naturelle ubiquitaire chez les plantes et impliquée… (more)

Subjects/Keywords: Nicotianamine; Thermonicotianamine; N-Alkylation; Synthèse en phase solide; Spectrométrie de masse; Nicotianamine; Thermonicotianamine; N-Alkylation; Supported synthesis; Mass sSpectrométriepectrometry

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APA (6th Edition):

Larrouy, M. (2010). Nouvelles synthèses totales de la nicotianamines et d'analogues : New strategies for total synthesis of nicotianamine and analogues. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2010MON20168

Chicago Manual of Style (16th Edition):

Larrouy, Manuel. “Nouvelles synthèses totales de la nicotianamines et d'analogues : New strategies for total synthesis of nicotianamine and analogues.” 2010. Doctoral Dissertation, Université Montpellier II. Accessed April 16, 2021. http://www.theses.fr/2010MON20168.

MLA Handbook (7th Edition):

Larrouy, Manuel. “Nouvelles synthèses totales de la nicotianamines et d'analogues : New strategies for total synthesis of nicotianamine and analogues.” 2010. Web. 16 Apr 2021.

Vancouver:

Larrouy M. Nouvelles synthèses totales de la nicotianamines et d'analogues : New strategies for total synthesis of nicotianamine and analogues. [Internet] [Doctoral dissertation]. Université Montpellier II; 2010. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2010MON20168.

Council of Science Editors:

Larrouy M. Nouvelles synthèses totales de la nicotianamines et d'analogues : New strategies for total synthesis of nicotianamine and analogues. [Doctoral Dissertation]. Université Montpellier II; 2010. Available from: http://www.theses.fr/2010MON20168


Boston College

4. Lee, Yunmi. Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes.

Degree: PhD, Chemistry, 2010, Boston College

 Chapter 1. In this chapter, the ability of chiral bidentate N-heterocyclic carbenes (NHCs) to activate alkylmetal reagents directly in order to promote C‒C bond forming… (more)

Subjects/Keywords: Cu-catalyzed reaction; Dihydroboration; Enantioselective Allylic Alkylation; Hydroboration; N-Heterocyclic carbene

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APA (6th Edition):

Lee, Y. (2010). Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101999

Chicago Manual of Style (16th Edition):

Lee, Yunmi. “Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes.” 2010. Doctoral Dissertation, Boston College. Accessed April 16, 2021. http://dlib.bc.edu/islandora/object/bc-ir:101999.

MLA Handbook (7th Edition):

Lee, Yunmi. “Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes.” 2010. Web. 16 Apr 2021.

Vancouver:

Lee Y. Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes. [Internet] [Doctoral dissertation]. Boston College; 2010. [cited 2021 Apr 16]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101999.

Council of Science Editors:

Lee Y. Site- and Enantioselective C-C and C-B Bond Forming Reactions Catalyzed by Cu-, Mg-, Zn-, or Al-based N-Heterocyclic Carbene Complexes. [Doctoral Dissertation]. Boston College; 2010. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101999


University of Bath

5. Al Badran, Firas. Reactor design : compact and catalytic for speciality chemicals.

Degree: PhD, 2011, University of Bath

 When speciality chemicals are manufactured within the pharmaceutical industry, they are often produced in stirred batch/semi-batch reactors. A ‘methodology’ was explored, to help with the… (more)

Subjects/Keywords: 660.2832; Continuous flow reactor; pharmaceutical industry; N-Alkylation; oxidation

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APA (6th Edition):

Al Badran, F. (2011). Reactor design : compact and catalytic for speciality chemicals. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/reactor-design-compact-and-catalytic-for-speciality-chemicals(e6dbdcc1-e46a-48ff-9ddc-aa10991c7c56).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545331

Chicago Manual of Style (16th Edition):

Al Badran, Firas. “Reactor design : compact and catalytic for speciality chemicals.” 2011. Doctoral Dissertation, University of Bath. Accessed April 16, 2021. https://researchportal.bath.ac.uk/en/studentthesis/reactor-design-compact-and-catalytic-for-speciality-chemicals(e6dbdcc1-e46a-48ff-9ddc-aa10991c7c56).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545331.

MLA Handbook (7th Edition):

Al Badran, Firas. “Reactor design : compact and catalytic for speciality chemicals.” 2011. Web. 16 Apr 2021.

Vancouver:

Al Badran F. Reactor design : compact and catalytic for speciality chemicals. [Internet] [Doctoral dissertation]. University of Bath; 2011. [cited 2021 Apr 16]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/reactor-design-compact-and-catalytic-for-speciality-chemicals(e6dbdcc1-e46a-48ff-9ddc-aa10991c7c56).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545331.

Council of Science Editors:

Al Badran F. Reactor design : compact and catalytic for speciality chemicals. [Doctoral Dissertation]. University of Bath; 2011. Available from: https://researchportal.bath.ac.uk/en/studentthesis/reactor-design-compact-and-catalytic-for-speciality-chemicals(e6dbdcc1-e46a-48ff-9ddc-aa10991c7c56).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545331


Universidade Federal de Santa Maria

6. Jefferson Trindade Filho. REACTION PARAMETERS INFLUENCE IN THE 3,5-DIMETHYL-1H-PYRAZOLE N-ALKYLATION UNDER MICROWAVE IRRADIATION.

Degree: 2012, Universidade Federal de Santa Maria

Este trabalho descreve a influência dos parâmetros reacionais sobre a N-alquilação de 3,5-dimetil-1H-pirazol assistida por irradiação de micro-ondas. Os experimentos foram conduzidos em diferentes condições… (more)

Subjects/Keywords: líquido iônico; pirazol; N-alquilação; micro-ondas; QUIMICA; microwave; N-alkylation; pyrazole; ionic liquid

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APA (6th Edition):

Filho, J. T. (2012). REACTION PARAMETERS INFLUENCE IN THE 3,5-DIMETHYL-1H-PYRAZOLE N-ALKYLATION UNDER MICROWAVE IRRADIATION. (Thesis). Universidade Federal de Santa Maria. Retrieved from http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=4579

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Filho, Jefferson Trindade. “REACTION PARAMETERS INFLUENCE IN THE 3,5-DIMETHYL-1H-PYRAZOLE N-ALKYLATION UNDER MICROWAVE IRRADIATION.” 2012. Thesis, Universidade Federal de Santa Maria. Accessed April 16, 2021. http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=4579.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Filho, Jefferson Trindade. “REACTION PARAMETERS INFLUENCE IN THE 3,5-DIMETHYL-1H-PYRAZOLE N-ALKYLATION UNDER MICROWAVE IRRADIATION.” 2012. Web. 16 Apr 2021.

Vancouver:

Filho JT. REACTION PARAMETERS INFLUENCE IN THE 3,5-DIMETHYL-1H-PYRAZOLE N-ALKYLATION UNDER MICROWAVE IRRADIATION. [Internet] [Thesis]. Universidade Federal de Santa Maria; 2012. [cited 2021 Apr 16]. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=4579.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Filho JT. REACTION PARAMETERS INFLUENCE IN THE 3,5-DIMETHYL-1H-PYRAZOLE N-ALKYLATION UNDER MICROWAVE IRRADIATION. [Thesis]. Universidade Federal de Santa Maria; 2012. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=4579

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of New Orleans

7. Lindsay, Maria. Studies directed Towards the Iridium Catalyzed Synthesis of New Carbon-Nitrogen Bonds.

Degree: PhD, Chemistry, 2017, University of New Orleans

  Amines are ubiquitous in nature and serve a variety of functions in living organisms. Because of this fact amines are of great biological and… (more)

Subjects/Keywords: Iridium; Catalysis; alpha-amino acid esters; N-alkylation; N-Heterocyclization; Medicinal-Pharmaceutical Chemistry; Organic Chemistry

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APA (6th Edition):

Lindsay, M. (2017). Studies directed Towards the Iridium Catalyzed Synthesis of New Carbon-Nitrogen Bonds. (Doctoral Dissertation). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/2336

Chicago Manual of Style (16th Edition):

Lindsay, Maria. “Studies directed Towards the Iridium Catalyzed Synthesis of New Carbon-Nitrogen Bonds.” 2017. Doctoral Dissertation, University of New Orleans. Accessed April 16, 2021. https://scholarworks.uno.edu/td/2336.

MLA Handbook (7th Edition):

Lindsay, Maria. “Studies directed Towards the Iridium Catalyzed Synthesis of New Carbon-Nitrogen Bonds.” 2017. Web. 16 Apr 2021.

Vancouver:

Lindsay M. Studies directed Towards the Iridium Catalyzed Synthesis of New Carbon-Nitrogen Bonds. [Internet] [Doctoral dissertation]. University of New Orleans; 2017. [cited 2021 Apr 16]. Available from: https://scholarworks.uno.edu/td/2336.

Council of Science Editors:

Lindsay M. Studies directed Towards the Iridium Catalyzed Synthesis of New Carbon-Nitrogen Bonds. [Doctoral Dissertation]. University of New Orleans; 2017. Available from: https://scholarworks.uno.edu/td/2336

8. Wahba, Amir E. New Synthetic Methodologies for the Construction and Optimization of Natural Products.

Degree: PhD, Pharmaceutical Sciences, 2011, University of Mississippi

 Toxicity associated with bioactive natural products is considered as a major obstacle in the process of drug discovery. Manzamine A (MA) is one such candidate… (more)

Subjects/Keywords: Decarboxylative Cross Coupling; Malaria; Manzamine Alkaloids; Reductive Amidation; Reductive N-Alkylation; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Wahba, A. E. (2011). New Synthetic Methodologies for the Construction and Optimization of Natural Products. (Doctoral Dissertation). University of Mississippi. Retrieved from https://egrove.olemiss.edu/etd/295

Chicago Manual of Style (16th Edition):

Wahba, Amir E. “New Synthetic Methodologies for the Construction and Optimization of Natural Products.” 2011. Doctoral Dissertation, University of Mississippi. Accessed April 16, 2021. https://egrove.olemiss.edu/etd/295.

MLA Handbook (7th Edition):

Wahba, Amir E. “New Synthetic Methodologies for the Construction and Optimization of Natural Products.” 2011. Web. 16 Apr 2021.

Vancouver:

Wahba AE. New Synthetic Methodologies for the Construction and Optimization of Natural Products. [Internet] [Doctoral dissertation]. University of Mississippi; 2011. [cited 2021 Apr 16]. Available from: https://egrove.olemiss.edu/etd/295.

Council of Science Editors:

Wahba AE. New Synthetic Methodologies for the Construction and Optimization of Natural Products. [Doctoral Dissertation]. University of Mississippi; 2011. Available from: https://egrove.olemiss.edu/etd/295


University of New Orleans

9. Bajaber, Majed Abdullah. Study of Iridium Catalyzed N-Alkylation of Urea with Benzyl Alcohols.

Degree: MS, Chemistry, 2014, University of New Orleans

  The solvent-free (Cp*IrCl2)2 catalyzed N-alkylation of urea with benzyl alcohol has been studied. A variety of reaction conditions were studied and optimized to produce… (more)

Subjects/Keywords: chemistry; organic; urea; N-alkylation, iridium, benzyl alcohol.; Natural Products Chemistry and Pharmacognosy

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APA (6th Edition):

Bajaber, M. A. (2014). Study of Iridium Catalyzed N-Alkylation of Urea with Benzyl Alcohols. (Thesis). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/1863

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Bajaber, Majed Abdullah. “Study of Iridium Catalyzed N-Alkylation of Urea with Benzyl Alcohols.” 2014. Thesis, University of New Orleans. Accessed April 16, 2021. https://scholarworks.uno.edu/td/1863.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Bajaber, Majed Abdullah. “Study of Iridium Catalyzed N-Alkylation of Urea with Benzyl Alcohols.” 2014. Web. 16 Apr 2021.

Vancouver:

Bajaber MA. Study of Iridium Catalyzed N-Alkylation of Urea with Benzyl Alcohols. [Internet] [Thesis]. University of New Orleans; 2014. [cited 2021 Apr 16]. Available from: https://scholarworks.uno.edu/td/1863.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Bajaber MA. Study of Iridium Catalyzed N-Alkylation of Urea with Benzyl Alcohols. [Thesis]. University of New Orleans; 2014. Available from: https://scholarworks.uno.edu/td/1863

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Brno University of Technology

10. Cigánek, Martin. Syntéza a studium nových derivátů diketopyrrolopyrrolů (DPPs) pro organickou elektroniku: The synthesis and study of new derivatives of diketopyrrolopyrroles for organic electronics.

Degree: 2018, Brno University of Technology

 This diploma thesis describes organic pigments of diketopyrrolopyrroles (DDPs) possessing properties applicable in attractive and perspective areas of organic electronics and photonics. The modification of… (more)

Subjects/Keywords: Diketopyrrolopyrrol; ethyladamantyl; organická elektronika; N-alkylace; -konjugace; ambipolární; Diketopyrrolopyrrole; ethyladamantyl; organic electronics; N-alkylation; -conjugation; ambipolar

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APA (6th Edition):

Cigánek, M. (2018). Syntéza a studium nových derivátů diketopyrrolopyrrolů (DPPs) pro organickou elektroniku: The synthesis and study of new derivatives of diketopyrrolopyrroles for organic electronics. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/65011

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Cigánek, Martin. “Syntéza a studium nových derivátů diketopyrrolopyrrolů (DPPs) pro organickou elektroniku: The synthesis and study of new derivatives of diketopyrrolopyrroles for organic electronics.” 2018. Thesis, Brno University of Technology. Accessed April 16, 2021. http://hdl.handle.net/11012/65011.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Cigánek, Martin. “Syntéza a studium nových derivátů diketopyrrolopyrrolů (DPPs) pro organickou elektroniku: The synthesis and study of new derivatives of diketopyrrolopyrroles for organic electronics.” 2018. Web. 16 Apr 2021.

Vancouver:

Cigánek M. Syntéza a studium nových derivátů diketopyrrolopyrrolů (DPPs) pro organickou elektroniku: The synthesis and study of new derivatives of diketopyrrolopyrroles for organic electronics. [Internet] [Thesis]. Brno University of Technology; 2018. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/11012/65011.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Cigánek M. Syntéza a studium nových derivátů diketopyrrolopyrrolů (DPPs) pro organickou elektroniku: The synthesis and study of new derivatives of diketopyrrolopyrroles for organic electronics. [Thesis]. Brno University of Technology; 2018. Available from: http://hdl.handle.net/11012/65011

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of New Orleans

11. Apsunde, Tushar D. Synthesis and Biological Evaluation of N-heterocycles for Activity on Monoamine Transporters and Exploration of Iridium Chemistry for Synthesis of Medicinally Important Molecules.

Degree: PhD, Chemistry, 2014, University of New Orleans

  The focus of these studies was directed towards the synthesis of novel N-heterocyclic compounds and pharmacological evaluation of these compounds for activity at monoamine… (more)

Subjects/Keywords: Dopamine, Serotonin, Methamphetamine, cocaine, N-heterocylization, Catalysis, Microwave, Nicotine, N-alkylation.; Medicinal-Pharmaceutical Chemistry; Organic Chemistry

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APA (6th Edition):

Apsunde, T. D. (2014). Synthesis and Biological Evaluation of N-heterocycles for Activity on Monoamine Transporters and Exploration of Iridium Chemistry for Synthesis of Medicinally Important Molecules. (Doctoral Dissertation). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/1862

Chicago Manual of Style (16th Edition):

Apsunde, Tushar D. “Synthesis and Biological Evaluation of N-heterocycles for Activity on Monoamine Transporters and Exploration of Iridium Chemistry for Synthesis of Medicinally Important Molecules.” 2014. Doctoral Dissertation, University of New Orleans. Accessed April 16, 2021. https://scholarworks.uno.edu/td/1862.

MLA Handbook (7th Edition):

Apsunde, Tushar D. “Synthesis and Biological Evaluation of N-heterocycles for Activity on Monoamine Transporters and Exploration of Iridium Chemistry for Synthesis of Medicinally Important Molecules.” 2014. Web. 16 Apr 2021.

Vancouver:

Apsunde TD. Synthesis and Biological Evaluation of N-heterocycles for Activity on Monoamine Transporters and Exploration of Iridium Chemistry for Synthesis of Medicinally Important Molecules. [Internet] [Doctoral dissertation]. University of New Orleans; 2014. [cited 2021 Apr 16]. Available from: https://scholarworks.uno.edu/td/1862.

Council of Science Editors:

Apsunde TD. Synthesis and Biological Evaluation of N-heterocycles for Activity on Monoamine Transporters and Exploration of Iridium Chemistry for Synthesis of Medicinally Important Molecules. [Doctoral Dissertation]. University of New Orleans; 2014. Available from: https://scholarworks.uno.edu/td/1862

12. Trindade Filho, Jefferson. Influência dos parâmetros reacionais na N-alquilação de 3,5-dimetil-1h-pirazol sob irradiação de micro-ondas.

Degree: 2012, Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

This work describes the reaction parameters influence in the 3,5-dimethyl-1H-pyrazole N-alkylation under microwave irradiation. The experiments were… (more)

Subjects/Keywords: Micro-ondas; N-alquilação; Pirazol; Líquido iônico; Microwave; N-alkylation; Pyrazole; Ionic liquid; CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA

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APA (6th Edition):

Trindade Filho, J. (2012). Influência dos parâmetros reacionais na N-alquilação de 3,5-dimetil-1h-pirazol sob irradiação de micro-ondas. (Masters Thesis). Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química. Retrieved from http://repositorio.ufsm.br/handle/1/10508

Chicago Manual of Style (16th Edition):

Trindade Filho, Jefferson. “Influência dos parâmetros reacionais na N-alquilação de 3,5-dimetil-1h-pirazol sob irradiação de micro-ondas.” 2012. Masters Thesis, Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química. Accessed April 16, 2021. http://repositorio.ufsm.br/handle/1/10508.

MLA Handbook (7th Edition):

Trindade Filho, Jefferson. “Influência dos parâmetros reacionais na N-alquilação de 3,5-dimetil-1h-pirazol sob irradiação de micro-ondas.” 2012. Web. 16 Apr 2021.

Vancouver:

Trindade Filho J. Influência dos parâmetros reacionais na N-alquilação de 3,5-dimetil-1h-pirazol sob irradiação de micro-ondas. [Internet] [Masters thesis]. Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química; 2012. [cited 2021 Apr 16]. Available from: http://repositorio.ufsm.br/handle/1/10508.

Council of Science Editors:

Trindade Filho J. Influência dos parâmetros reacionais na N-alquilação de 3,5-dimetil-1h-pirazol sob irradiação de micro-ondas. [Masters Thesis]. Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química; 2012. Available from: http://repositorio.ufsm.br/handle/1/10508

13. Pereira, Fernanda Stuani [UNESP]. Estudos de biopolímeros a base de quitina e quitosana quimicamente transformados para quelação de metais e para a captura e fixação de dióxido de carbono.

Degree: 2016, Universidade Estadual Paulista (UNESP)

Submitted by Fernanda Stuani Pereira null ([email protected]) on 2016-06-22T22:22:49Z No. of bitstreams: 1 Tese-FERNANDA STUANI PEREIRA.pdf: 6105856 bytes, checksum: 653cf59956934017da496664aa74e886 (MD5)

Approved for entry into… (more)

Subjects/Keywords: Quitosana; N-Alquilação; Poli-azo-compostos; Complexos de Cu(II); Complexos de Zn(II); Chitosan; N-alkylation; Poly-azo-compounds

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APA (6th Edition):

Pereira, F. S. [. (2016). Estudos de biopolímeros a base de quitina e quitosana quimicamente transformados para quelação de metais e para a captura e fixação de dióxido de carbono. (Doctoral Dissertation). Universidade Estadual Paulista (UNESP). Retrieved from http://hdl.handle.net/11449/139534

Chicago Manual of Style (16th Edition):

Pereira, Fernanda Stuani [UNESP]. “Estudos de biopolímeros a base de quitina e quitosana quimicamente transformados para quelação de metais e para a captura e fixação de dióxido de carbono.” 2016. Doctoral Dissertation, Universidade Estadual Paulista (UNESP). Accessed April 16, 2021. http://hdl.handle.net/11449/139534.

MLA Handbook (7th Edition):

Pereira, Fernanda Stuani [UNESP]. “Estudos de biopolímeros a base de quitina e quitosana quimicamente transformados para quelação de metais e para a captura e fixação de dióxido de carbono.” 2016. Web. 16 Apr 2021.

Vancouver:

Pereira FS[. Estudos de biopolímeros a base de quitina e quitosana quimicamente transformados para quelação de metais e para a captura e fixação de dióxido de carbono. [Internet] [Doctoral dissertation]. Universidade Estadual Paulista (UNESP); 2016. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/11449/139534.

Council of Science Editors:

Pereira FS[. Estudos de biopolímeros a base de quitina e quitosana quimicamente transformados para quelação de metais e para a captura e fixação de dióxido de carbono. [Doctoral Dissertation]. Universidade Estadual Paulista (UNESP); 2016. Available from: http://hdl.handle.net/11449/139534

14. El Asaad, Bilal. Synthesis of Optically Pure Nitrogenated Ligands and their uses in Asymmetric Catalysis : Synthèses des ligands azotés optiquement pures pour leurs utilisations en catalyse asymétrique.

Degree: Docteur es, Chimie, 2017, Lyon; Université libanaise

Des nouveaux ligands chiraux diamine N-aromatiques, dérivés de 1,2-diaminocyclohexane et des a et ß- cétones cycliques aromatiques, ont été synthétisés par alkylation-déshydrogénation catalysée par le… (more)

Subjects/Keywords: N-Diaryl Diamine Chiraux; Alkylation-deshydrogénation; Transfert d'hydrure asymétrique des cétones aromatiques; Iridium; Réaction de henry asymétrique; Cuivre (II); N; N-diaryl diamine; Dehydrogenative alkylation; Asymmetric transfer hydrogenationof aromatic ketones; Iridium; Asymmetric Henry Reaction; Copper (II); Chiral N; 547

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APA (6th Edition):

El Asaad, B. (2017). Synthesis of Optically Pure Nitrogenated Ligands and their uses in Asymmetric Catalysis : Synthèses des ligands azotés optiquement pures pour leurs utilisations en catalyse asymétrique. (Doctoral Dissertation). Lyon; Université libanaise. Retrieved from http://www.theses.fr/2017LYSE1119

Chicago Manual of Style (16th Edition):

El Asaad, Bilal. “Synthesis of Optically Pure Nitrogenated Ligands and their uses in Asymmetric Catalysis : Synthèses des ligands azotés optiquement pures pour leurs utilisations en catalyse asymétrique.” 2017. Doctoral Dissertation, Lyon; Université libanaise. Accessed April 16, 2021. http://www.theses.fr/2017LYSE1119.

MLA Handbook (7th Edition):

El Asaad, Bilal. “Synthesis of Optically Pure Nitrogenated Ligands and their uses in Asymmetric Catalysis : Synthèses des ligands azotés optiquement pures pour leurs utilisations en catalyse asymétrique.” 2017. Web. 16 Apr 2021.

Vancouver:

El Asaad B. Synthesis of Optically Pure Nitrogenated Ligands and their uses in Asymmetric Catalysis : Synthèses des ligands azotés optiquement pures pour leurs utilisations en catalyse asymétrique. [Internet] [Doctoral dissertation]. Lyon; Université libanaise; 2017. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2017LYSE1119.

Council of Science Editors:

El Asaad B. Synthesis of Optically Pure Nitrogenated Ligands and their uses in Asymmetric Catalysis : Synthèses des ligands azotés optiquement pures pour leurs utilisations en catalyse asymétrique. [Doctoral Dissertation]. Lyon; Université libanaise; 2017. Available from: http://www.theses.fr/2017LYSE1119

15. Ren, Xiaoyu. Synthèse et réactivité de complexes métalliques porteurs de ligands carbéniques N-hétérocycliques fonctionnels : Synthesis and reactivity of metal complexes bearing functional N-heterocyclic carbene ligands.

Degree: Docteur es, Chimie, 2017, Université de Strasbourg

Des ligands hydrides potentiellement bidentes (possédant un donneur N-hétérocyclique (NHC) associé à un groupement donneur éther ou amine) ainsi que des ligands tritopiques de type… (more)

Subjects/Keywords: Ligands tritopiques de type pinceur; Addition oxydante; Alkylation; Oligomérisation de l’éthylène; N-heterocyclic carbenes; Tritopic pincer ligands; Oxidative addition; Alkylation; Ethylene oligomerization; 547.2

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APA (6th Edition):

Ren, X. (2017). Synthèse et réactivité de complexes métalliques porteurs de ligands carbéniques N-hétérocycliques fonctionnels : Synthesis and reactivity of metal complexes bearing functional N-heterocyclic carbene ligands. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAF081

Chicago Manual of Style (16th Edition):

Ren, Xiaoyu. “Synthèse et réactivité de complexes métalliques porteurs de ligands carbéniques N-hétérocycliques fonctionnels : Synthesis and reactivity of metal complexes bearing functional N-heterocyclic carbene ligands.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed April 16, 2021. http://www.theses.fr/2017STRAF081.

MLA Handbook (7th Edition):

Ren, Xiaoyu. “Synthèse et réactivité de complexes métalliques porteurs de ligands carbéniques N-hétérocycliques fonctionnels : Synthesis and reactivity of metal complexes bearing functional N-heterocyclic carbene ligands.” 2017. Web. 16 Apr 2021.

Vancouver:

Ren X. Synthèse et réactivité de complexes métalliques porteurs de ligands carbéniques N-hétérocycliques fonctionnels : Synthesis and reactivity of metal complexes bearing functional N-heterocyclic carbene ligands. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2017STRAF081.

Council of Science Editors:

Ren X. Synthèse et réactivité de complexes métalliques porteurs de ligands carbéniques N-hétérocycliques fonctionnels : Synthesis and reactivity of metal complexes bearing functional N-heterocyclic carbene ligands. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAF081


University of Bath

16. Hamid, Malai H. S. A. Conversion of alcohols into amines by borrowing hydrogen.

Degree: PhD, 2008, University of Bath

 This thesis describes the development of a more economical catalytic system for the N-alkylation of amines by “borrowing hydrogen” and its application in the synthesis… (more)

Subjects/Keywords: 547.042; catalysis; amination; N-Alkylation; Amines; ruthenium

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APA (6th Edition):

Hamid, M. H. S. A. (2008). Conversion of alcohols into amines by borrowing hydrogen. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/conversion-of-alcohols-into-amines-by-borrowing-hydrogen(f6e1c526-22c8-4e3d-b7af-7c385020380b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501635

Chicago Manual of Style (16th Edition):

Hamid, Malai H S A. “Conversion of alcohols into amines by borrowing hydrogen.” 2008. Doctoral Dissertation, University of Bath. Accessed April 16, 2021. https://researchportal.bath.ac.uk/en/studentthesis/conversion-of-alcohols-into-amines-by-borrowing-hydrogen(f6e1c526-22c8-4e3d-b7af-7c385020380b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501635.

MLA Handbook (7th Edition):

Hamid, Malai H S A. “Conversion of alcohols into amines by borrowing hydrogen.” 2008. Web. 16 Apr 2021.

Vancouver:

Hamid MHSA. Conversion of alcohols into amines by borrowing hydrogen. [Internet] [Doctoral dissertation]. University of Bath; 2008. [cited 2021 Apr 16]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/conversion-of-alcohols-into-amines-by-borrowing-hydrogen(f6e1c526-22c8-4e3d-b7af-7c385020380b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501635.

Council of Science Editors:

Hamid MHSA. Conversion of alcohols into amines by borrowing hydrogen. [Doctoral Dissertation]. University of Bath; 2008. Available from: https://researchportal.bath.ac.uk/en/studentthesis/conversion-of-alcohols-into-amines-by-borrowing-hydrogen(f6e1c526-22c8-4e3d-b7af-7c385020380b).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501635


University College Cork

17. Mackey, Pamela. Studies in asymmetric synthesis: I. the asymmetric α-alkylation of N,N-dimethylhydrazones II. the asymmetric aldol-Tishchenko reaction of (S)-tert-butanesulfinyl imines for the introduction of 2, 3, 4 and 5 new chiral centres in one pot.

Degree: 2020, University College Cork

 This thesis is split into two sections based on two different areas of research. Part 1 The asymmetric α-alkylation of ketones is one of the… (more)

Subjects/Keywords: Asymmetric α-alkylation; N-dimethylhydrazones; N; Aldol-Tishchenko reaction; Anti-1; 3-Amino alcohol derivatives; Double aldol-Tishchenko reaction; 3-Amino-1; 5-Diol derivatives; Contiguous chiral centres; DFT; (-)-Sparteine

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APA (6th Edition):

Mackey, P. (2020). Studies in asymmetric synthesis: I. the asymmetric α-alkylation of N,N-dimethylhydrazones II. the asymmetric aldol-Tishchenko reaction of (S)-tert-butanesulfinyl imines for the introduction of 2, 3, 4 and 5 new chiral centres in one pot. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/10484

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mackey, Pamela. “Studies in asymmetric synthesis: I. the asymmetric α-alkylation of N,N-dimethylhydrazones II. the asymmetric aldol-Tishchenko reaction of (S)-tert-butanesulfinyl imines for the introduction of 2, 3, 4 and 5 new chiral centres in one pot.” 2020. Thesis, University College Cork. Accessed April 16, 2021. http://hdl.handle.net/10468/10484.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mackey, Pamela. “Studies in asymmetric synthesis: I. the asymmetric α-alkylation of N,N-dimethylhydrazones II. the asymmetric aldol-Tishchenko reaction of (S)-tert-butanesulfinyl imines for the introduction of 2, 3, 4 and 5 new chiral centres in one pot.” 2020. Web. 16 Apr 2021.

Vancouver:

Mackey P. Studies in asymmetric synthesis: I. the asymmetric α-alkylation of N,N-dimethylhydrazones II. the asymmetric aldol-Tishchenko reaction of (S)-tert-butanesulfinyl imines for the introduction of 2, 3, 4 and 5 new chiral centres in one pot. [Internet] [Thesis]. University College Cork; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10468/10484.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mackey P. Studies in asymmetric synthesis: I. the asymmetric α-alkylation of N,N-dimethylhydrazones II. the asymmetric aldol-Tishchenko reaction of (S)-tert-butanesulfinyl imines for the introduction of 2, 3, 4 and 5 new chiral centres in one pot. [Thesis]. University College Cork; 2020. Available from: http://hdl.handle.net/10468/10484

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

18. Moraes, Paulo Alexandre de. N-alquilação regiosseletiva de pirazóis empregando 4-alcóxi(amino)-5-bromo-1,1,1-trifluorpent-3-en-2-onas.

Degree: 2016, Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química

This work presents the synthesis of three new series of nitrogen-heterocycles containing the substituent trifluoromethyl, exploiting the synthetic versatility and regioselectivity of 4-alkoxy-5-bromo-1,1,1-trifluorpent-3-en-2-ones and 4-amino-5-bromo-1,1,1-trifluoropent-3-en-2-ones… (more)

Subjects/Keywords: Pirazol; Trifluormetil; Furano; Enonas; Enaminonas; Bromo; Adição de Michael; N-alquilacão; Pyrazole trifluoromethyl; Furan; Enones; Enaminones; Bromine; Michael addition; N-alkylation; CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA

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APA (6th Edition):

Moraes, P. A. d. (2016). N-alquilação regiosseletiva de pirazóis empregando 4-alcóxi(amino)-5-bromo-1,1,1-trifluorpent-3-en-2-onas. (Masters Thesis). Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química. Retrieved from http://repositorio.ufsm.br/handle/1/10628

Chicago Manual of Style (16th Edition):

Moraes, Paulo Alexandre de. “N-alquilação regiosseletiva de pirazóis empregando 4-alcóxi(amino)-5-bromo-1,1,1-trifluorpent-3-en-2-onas.” 2016. Masters Thesis, Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química. Accessed April 16, 2021. http://repositorio.ufsm.br/handle/1/10628.

MLA Handbook (7th Edition):

Moraes, Paulo Alexandre de. “N-alquilação regiosseletiva de pirazóis empregando 4-alcóxi(amino)-5-bromo-1,1,1-trifluorpent-3-en-2-onas.” 2016. Web. 16 Apr 2021.

Vancouver:

Moraes PAd. N-alquilação regiosseletiva de pirazóis empregando 4-alcóxi(amino)-5-bromo-1,1,1-trifluorpent-3-en-2-onas. [Internet] [Masters thesis]. Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química; 2016. [cited 2021 Apr 16]. Available from: http://repositorio.ufsm.br/handle/1/10628.

Council of Science Editors:

Moraes PAd. N-alquilação regiosseletiva de pirazóis empregando 4-alcóxi(amino)-5-bromo-1,1,1-trifluorpent-3-en-2-onas. [Masters Thesis]. Universidade Federal de Santa Maria; Programa de Pós-Graduação em Química; UFSM; BR; Química; 2016. Available from: http://repositorio.ufsm.br/handle/1/10628

19. Peyrat, Sandrine. Vers la synthèse de C-glycosyl aminoxy peptides et d'oligomères de nucléosides aminoxy acides : Towards the synthesis of C-glycosyl aminoxy peptides and oligomers of nucleosides aminoxy acids.

Degree: Docteur es, Chimie, 2011, Cachan, Ecole normale supérieure

Récemment, de nombreux efforts ont été consacrés au développement d’oligonucléotides synthétiques pour des applications thérapeutiques et de diagnostique variées. Les oligonucléotides modifiés peuvent inhiber sélectivement… (more)

Subjects/Keywords: Alkylation; Aminoxy acides; C-glycosyl aminoxy acides; Liaisons N-oxy amide, oxime et aminoxy; Mitsunobu; Dinucléosides; Nucléosides; Oligonucléotides modifiés; Wittig; Aminoxy acids nucleosides; N-oxy amide; Oxime and aminoxy linkage; C-glycosyl aminoxy acids; Dinucleosides; Modified oligonucleotides; Mitsunobu; Alkylation; Wittig

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APA (6th Edition):

Peyrat, S. (2011). Vers la synthèse de C-glycosyl aminoxy peptides et d'oligomères de nucléosides aminoxy acides : Towards the synthesis of C-glycosyl aminoxy peptides and oligomers of nucleosides aminoxy acids. (Doctoral Dissertation). Cachan, Ecole normale supérieure. Retrieved from http://www.theses.fr/2011DENS0065

Chicago Manual of Style (16th Edition):

Peyrat, Sandrine. “Vers la synthèse de C-glycosyl aminoxy peptides et d'oligomères de nucléosides aminoxy acides : Towards the synthesis of C-glycosyl aminoxy peptides and oligomers of nucleosides aminoxy acids.” 2011. Doctoral Dissertation, Cachan, Ecole normale supérieure. Accessed April 16, 2021. http://www.theses.fr/2011DENS0065.

MLA Handbook (7th Edition):

Peyrat, Sandrine. “Vers la synthèse de C-glycosyl aminoxy peptides et d'oligomères de nucléosides aminoxy acides : Towards the synthesis of C-glycosyl aminoxy peptides and oligomers of nucleosides aminoxy acids.” 2011. Web. 16 Apr 2021.

Vancouver:

Peyrat S. Vers la synthèse de C-glycosyl aminoxy peptides et d'oligomères de nucléosides aminoxy acides : Towards the synthesis of C-glycosyl aminoxy peptides and oligomers of nucleosides aminoxy acids. [Internet] [Doctoral dissertation]. Cachan, Ecole normale supérieure; 2011. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2011DENS0065.

Council of Science Editors:

Peyrat S. Vers la synthèse de C-glycosyl aminoxy peptides et d'oligomères de nucléosides aminoxy acides : Towards the synthesis of C-glycosyl aminoxy peptides and oligomers of nucleosides aminoxy acids. [Doctoral Dissertation]. Cachan, Ecole normale supérieure; 2011. Available from: http://www.theses.fr/2011DENS0065

20. Lemouzy, Sébastien. Synthèse stéréospécifique et chimie de coordination de ligands hétérobifonctionnels P-stéréogènes : vers le développement de méthodologies de couplages C-C palladocatalysés : Stereospecific synthesis and coordination chemistry of P-stereogenic heterobidentate ligands : towards the development of palladium-catalyzed C-C couplings.

Degree: Docteur es, Sciences Chimiques. Chimie organique, 2016, Aix Marseille Université

La première partie de ce manuscrit traite de la synthèse de phosphine-boranes P-stéréogènes énantioenrichis à partir d’un précurseur développé par notre laboratoire : le H-phénylphosphinate… (more)

Subjects/Keywords: Phosphore; P-Stéréogène; Réduction; Phosphures masqués; Alkylation; Ligands P-N; Palladium; Catalyse; Couplages C-C; Phosphorus chemistry; P-Stereogenic; Stereospecific; Reduction; Masked phosphido-Boranes; Alkylation; P-N ligands; Palladium; Catalysis; C-C coupling.

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APA (6th Edition):

Lemouzy, S. (2016). Synthèse stéréospécifique et chimie de coordination de ligands hétérobifonctionnels P-stéréogènes : vers le développement de méthodologies de couplages C-C palladocatalysés : Stereospecific synthesis and coordination chemistry of P-stereogenic heterobidentate ligands : towards the development of palladium-catalyzed C-C couplings. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM4359

Chicago Manual of Style (16th Edition):

Lemouzy, Sébastien. “Synthèse stéréospécifique et chimie de coordination de ligands hétérobifonctionnels P-stéréogènes : vers le développement de méthodologies de couplages C-C palladocatalysés : Stereospecific synthesis and coordination chemistry of P-stereogenic heterobidentate ligands : towards the development of palladium-catalyzed C-C couplings.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed April 16, 2021. http://www.theses.fr/2016AIXM4359.

MLA Handbook (7th Edition):

Lemouzy, Sébastien. “Synthèse stéréospécifique et chimie de coordination de ligands hétérobifonctionnels P-stéréogènes : vers le développement de méthodologies de couplages C-C palladocatalysés : Stereospecific synthesis and coordination chemistry of P-stereogenic heterobidentate ligands : towards the development of palladium-catalyzed C-C couplings.” 2016. Web. 16 Apr 2021.

Vancouver:

Lemouzy S. Synthèse stéréospécifique et chimie de coordination de ligands hétérobifonctionnels P-stéréogènes : vers le développement de méthodologies de couplages C-C palladocatalysés : Stereospecific synthesis and coordination chemistry of P-stereogenic heterobidentate ligands : towards the development of palladium-catalyzed C-C couplings. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2016AIXM4359.

Council of Science Editors:

Lemouzy S. Synthèse stéréospécifique et chimie de coordination de ligands hétérobifonctionnels P-stéréogènes : vers le développement de méthodologies de couplages C-C palladocatalysés : Stereospecific synthesis and coordination chemistry of P-stereogenic heterobidentate ligands : towards the development of palladium-catalyzed C-C couplings. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM4359

21. LIU HUIHUI. Supported Group II Transition Metal Catalysts in Liquid Phase Reactions using Borrowing Hydrogen Methodology.

Degree: 2013, National University of Singapore

Subjects/Keywords: Borrowing Hydrogen; Silver; Copper; Heterogeneous catalysis; N-alkylation reaction; Coupling reaction

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APA (6th Edition):

HUIHUI, L. (2013). Supported Group II Transition Metal Catalysts in Liquid Phase Reactions using Borrowing Hydrogen Methodology. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/48686

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

HUIHUI, LIU. “Supported Group II Transition Metal Catalysts in Liquid Phase Reactions using Borrowing Hydrogen Methodology.” 2013. Thesis, National University of Singapore. Accessed April 16, 2021. http://scholarbank.nus.edu.sg/handle/10635/48686.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

HUIHUI, LIU. “Supported Group II Transition Metal Catalysts in Liquid Phase Reactions using Borrowing Hydrogen Methodology.” 2013. Web. 16 Apr 2021.

Vancouver:

HUIHUI L. Supported Group II Transition Metal Catalysts in Liquid Phase Reactions using Borrowing Hydrogen Methodology. [Internet] [Thesis]. National University of Singapore; 2013. [cited 2021 Apr 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/48686.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

HUIHUI L. Supported Group II Transition Metal Catalysts in Liquid Phase Reactions using Borrowing Hydrogen Methodology. [Thesis]. National University of Singapore; 2013. Available from: http://scholarbank.nus.edu.sg/handle/10635/48686

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Sherbrooke

22. Guérin, Vincent. Étude de ligands reposant sur des ylures de N-iminoimidazolium.

Degree: 2021, Université de Sherbrooke

 Nous allons nous intéresser dans cet ouvrage à l’utilisation d’ylures de N-iminoimidazolium comme proligands NHC (carbène N-hétérocyclique) anionique en catalyse organométallique. L’introduction rapporte tout d’abord… (more)

Subjects/Keywords: Chimie organométallique; Chimie organique; Carbène N-hétérocyclique; NHC; Ligand; Iridium; Palladium; Mode de liaison; Réaction de Suzuki-Miyaura; Réaction de Tsuji-Trost; Alkylation d’amines; Emprun d’hydrogène; Piégeage d’énolate; Iode hypervalent

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APA (6th Edition):

Guérin, V. (2021). Étude de ligands reposant sur des ylures de N-iminoimidazolium. (Doctoral Dissertation). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/18016

Chicago Manual of Style (16th Edition):

Guérin, Vincent. “Étude de ligands reposant sur des ylures de N-iminoimidazolium.” 2021. Doctoral Dissertation, Université de Sherbrooke. Accessed April 16, 2021. http://hdl.handle.net/11143/18016.

MLA Handbook (7th Edition):

Guérin, Vincent. “Étude de ligands reposant sur des ylures de N-iminoimidazolium.” 2021. Web. 16 Apr 2021.

Vancouver:

Guérin V. Étude de ligands reposant sur des ylures de N-iminoimidazolium. [Internet] [Doctoral dissertation]. Université de Sherbrooke; 2021. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/11143/18016.

Council of Science Editors:

Guérin V. Étude de ligands reposant sur des ylures de N-iminoimidazolium. [Doctoral Dissertation]. Université de Sherbrooke; 2021. Available from: http://hdl.handle.net/11143/18016


Kyoto University / 京都大学

23. Chang, Yunghung. Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium : PNPピンサー型ホスファアルケンイリジウム錯体に関する研究.

Degree: 博士(工学), 2014, Kyoto University / 京都大学

新制・課程博士

甲第18471号

工博第3907号

Subjects/Keywords: PNP-pincer iridium complexes; phosphaalkene ligands; N–H bond cleavage; C–H bond cleavage; N-alkylation

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APA (6th Edition):

Chang, Y. (2014). Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium : PNPピンサー型ホスファアルケンイリジウム錯体に関する研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/189364 ; http://dx.doi.org/10.14989/doctor.k18471

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chang, Yunghung. “Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium : PNPピンサー型ホスファアルケンイリジウム錯体に関する研究.” 2014. Thesis, Kyoto University / 京都大学. Accessed April 16, 2021. http://hdl.handle.net/2433/189364 ; http://dx.doi.org/10.14989/doctor.k18471.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chang, Yunghung. “Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium : PNPピンサー型ホスファアルケンイリジウム錯体に関する研究.” 2014. Web. 16 Apr 2021.

Vancouver:

Chang Y. Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium : PNPピンサー型ホスファアルケンイリジウム錯体に関する研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/2433/189364 ; http://dx.doi.org/10.14989/doctor.k18471.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chang Y. Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium : PNPピンサー型ホスファアルケンイリジウム錯体に関する研究. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/189364 ; http://dx.doi.org/10.14989/doctor.k18471

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Kyoto University

24. Chang, Yunghung. Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium .

Degree: 2014, Kyoto University

Subjects/Keywords: PNP-pincer iridium complexes; phosphaalkene ligands; N–H bond cleavage; C–H bond cleavage; N-alkylation

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Chang, Y. (2014). Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/189364

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chang, Yunghung. “Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium .” 2014. Thesis, Kyoto University. Accessed April 16, 2021. http://hdl.handle.net/2433/189364.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chang, Yunghung. “Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium .” 2014. Web. 16 Apr 2021.

Vancouver:

Chang Y. Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium . [Internet] [Thesis]. Kyoto University; 2014. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/2433/189364.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chang Y. Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium . [Thesis]. Kyoto University; 2014. Available from: http://hdl.handle.net/2433/189364

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

25. Thota, Kiran Kumar. Studies Directed Toward the Synthesis of Amphibian Alkaloids via Iridium Catalyzed N-Heterocyclization Reactions.

Degree: PhD, Chemistry, 2014, University of New Orleans

  The pyrrolidine and piperidine ring systems are present in a variety of different classes of amphibian alkaloids. We have found the iridium catalyzed N-heterocylization… (more)

Subjects/Keywords: N-heterocyclization; Microwave; N-alkylation; Iridium; amphibian alkaloids; hydroboration; Organic Chemistry

…Table 1.23 N-alkylation of aqueous ammonia with a variety of secondary alcohols catalyzed… …19 Scheme 1.5 Possible catalytic cycle for Ir catalyzed N-alkylation… …are also discussed. xi Keywords: N-Heterocyclization, Catalysis, Microwave, N-Alkylation… …Catalyzed NHeterocyclization with Alcohols 1.1 Iridium catalyzed N-alkylation using alcohols N… …x28;Cp*= pentamethylcyclopentadienyl) for the N-alkylation of amines with primary and… 

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APA (6th Edition):

Thota, K. K. (2014). Studies Directed Toward the Synthesis of Amphibian Alkaloids via Iridium Catalyzed N-Heterocyclization Reactions. (Doctoral Dissertation). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/1950

Chicago Manual of Style (16th Edition):

Thota, Kiran Kumar. “Studies Directed Toward the Synthesis of Amphibian Alkaloids via Iridium Catalyzed N-Heterocyclization Reactions.” 2014. Doctoral Dissertation, University of New Orleans. Accessed April 16, 2021. https://scholarworks.uno.edu/td/1950.

MLA Handbook (7th Edition):

Thota, Kiran Kumar. “Studies Directed Toward the Synthesis of Amphibian Alkaloids via Iridium Catalyzed N-Heterocyclization Reactions.” 2014. Web. 16 Apr 2021.

Vancouver:

Thota KK. Studies Directed Toward the Synthesis of Amphibian Alkaloids via Iridium Catalyzed N-Heterocyclization Reactions. [Internet] [Doctoral dissertation]. University of New Orleans; 2014. [cited 2021 Apr 16]. Available from: https://scholarworks.uno.edu/td/1950.

Council of Science Editors:

Thota KK. Studies Directed Toward the Synthesis of Amphibian Alkaloids via Iridium Catalyzed N-Heterocyclization Reactions. [Doctoral Dissertation]. University of New Orleans; 2014. Available from: https://scholarworks.uno.edu/td/1950

26. Magalhães, Hernane Tolentino. Síntese sequencial linear de 6-((1,2,3-triazol-4-il)metil)-4,5- dimetil-2,6-di-hidro-1h-pirrolo[3,4-d]piridazinonas via reações de N-alquilação, CuAAC e ciclocondensação.

Degree: 2017, Universidade Federal de Santa Maria; Centro de Ciências Naturais e Exatas; Programa de Pós-Graduação em Química; UFSM; Brasil; Química

This dissertation presents a synthetic route for obtaining a series of eight 6-((1H-1,2,3- triazol-4-yl)methyl)-1H-pyrrolo[3,4-d]pyridazin-1-ones with yields of 40-70%. The synthetic route comprises three distinct steps:… (more)

Subjects/Keywords: Pirróis; Triazóis; Pirrolo[3,4-d]piridazinonas; N-alquilação; CuAAC; Reação de ciclocondensação [4+2] com hidrazinas; HCl; Pyrroles; Triazoles; Pyrrolo[3,4-d]pyridazinones; N-alkylation; CuAAC; [4+2] cyclocondesation reaction with hydrazine; CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA

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APA (6th Edition):

Magalhães, H. T. (2017). Síntese sequencial linear de 6-((1,2,3-triazol-4-il)metil)-4,5- dimetil-2,6-di-hidro-1h-pirrolo[3,4-d]piridazinonas via reações de N-alquilação, CuAAC e ciclocondensação. (Masters Thesis). Universidade Federal de Santa Maria; Centro de Ciências Naturais e Exatas; Programa de Pós-Graduação em Química; UFSM; Brasil; Química. Retrieved from http://repositorio.ufsm.br/handle/1/15179

Chicago Manual of Style (16th Edition):

Magalhães, Hernane Tolentino. “Síntese sequencial linear de 6-((1,2,3-triazol-4-il)metil)-4,5- dimetil-2,6-di-hidro-1h-pirrolo[3,4-d]piridazinonas via reações de N-alquilação, CuAAC e ciclocondensação.” 2017. Masters Thesis, Universidade Federal de Santa Maria; Centro de Ciências Naturais e Exatas; Programa de Pós-Graduação em Química; UFSM; Brasil; Química. Accessed April 16, 2021. http://repositorio.ufsm.br/handle/1/15179.

MLA Handbook (7th Edition):

Magalhães, Hernane Tolentino. “Síntese sequencial linear de 6-((1,2,3-triazol-4-il)metil)-4,5- dimetil-2,6-di-hidro-1h-pirrolo[3,4-d]piridazinonas via reações de N-alquilação, CuAAC e ciclocondensação.” 2017. Web. 16 Apr 2021.

Vancouver:

Magalhães HT. Síntese sequencial linear de 6-((1,2,3-triazol-4-il)metil)-4,5- dimetil-2,6-di-hidro-1h-pirrolo[3,4-d]piridazinonas via reações de N-alquilação, CuAAC e ciclocondensação. [Internet] [Masters thesis]. Universidade Federal de Santa Maria; Centro de Ciências Naturais e Exatas; Programa de Pós-Graduação em Química; UFSM; Brasil; Química; 2017. [cited 2021 Apr 16]. Available from: http://repositorio.ufsm.br/handle/1/15179.

Council of Science Editors:

Magalhães HT. Síntese sequencial linear de 6-((1,2,3-triazol-4-il)metil)-4,5- dimetil-2,6-di-hidro-1h-pirrolo[3,4-d]piridazinonas via reações de N-alquilação, CuAAC e ciclocondensação. [Masters Thesis]. Universidade Federal de Santa Maria; Centro de Ciências Naturais e Exatas; Programa de Pós-Graduação em Química; UFSM; Brasil; Química; 2017. Available from: http://repositorio.ufsm.br/handle/1/15179


Université de Sherbrooke

27. Komba, Jeampy Etambala. Relation entre la vitamine C oxydée (DHA) et l’homocystéine thiolactone: Relationship between oxidized vitamin C and homocysteine thiolactone.

Degree: 2021, Université de Sherbrooke

 Abstract : Homocysteine thiolactone (HcyTL) is a metabolite of homocysteine (HcySH) that occurs during a metabolic error of the enzyme methionyl-tRNA synthetase mistakenly selecting methionine… (more)

Subjects/Keywords: Acide déhydroascorbique; Homocystéine thiolactone; Insuline; Cytochrome C; α-Lactalbumine; Hémoglobine; N-homocystéinylation; S-Alkylation; Ionisation par électronébulsation; Spectrométrie de masse; Dehydroascorbic acid; Homocysteine thiolactone; Insulin; α-Lactalbumin; Hemoglobin; N-homocysteinylation; Electronbulsation ionization; Mass spectrometry

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APA (6th Edition):

Komba, J. E. (2021). Relation entre la vitamine C oxydée (DHA) et l’homocystéine thiolactone: Relationship between oxidized vitamin C and homocysteine thiolactone. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/17917

Chicago Manual of Style (16th Edition):

Komba, Jeampy Etambala. “Relation entre la vitamine C oxydée (DHA) et l’homocystéine thiolactone: Relationship between oxidized vitamin C and homocysteine thiolactone.” 2021. Masters Thesis, Université de Sherbrooke. Accessed April 16, 2021. http://hdl.handle.net/11143/17917.

MLA Handbook (7th Edition):

Komba, Jeampy Etambala. “Relation entre la vitamine C oxydée (DHA) et l’homocystéine thiolactone: Relationship between oxidized vitamin C and homocysteine thiolactone.” 2021. Web. 16 Apr 2021.

Vancouver:

Komba JE. Relation entre la vitamine C oxydée (DHA) et l’homocystéine thiolactone: Relationship between oxidized vitamin C and homocysteine thiolactone. [Internet] [Masters thesis]. Université de Sherbrooke; 2021. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/11143/17917.

Council of Science Editors:

Komba JE. Relation entre la vitamine C oxydée (DHA) et l’homocystéine thiolactone: Relationship between oxidized vitamin C and homocysteine thiolactone. [Masters Thesis]. Université de Sherbrooke; 2021. Available from: http://hdl.handle.net/11143/17917

28. Chignen Possi, Kelvine. Synthèse des analogues de l’[azaPhe4]-GHRP-6 comme potentiels modulateurs du récepteur CD36.

Degree: 2018, Université de Montréal

Subjects/Keywords: Mimes peptidiques; Azapeptides; N-alkylation régio-sélective; GHRP-6; Récepteur CD36; N-alkylation; Relation entre la structure et l’activité biologique; Peptide mimes; Azapeptides; Regioselective N-alkylation; Receptor CD36; Structure-activity relationships; Chemistry - Pharmaceutical / Chimie pharmaceutique (UMI : 0491)

…Schéma 1.3 : Alkylation régiosélective du dipeptide benzhydrylidene glycine et aza-glycine en… …aza » aminé BEMP 2-(tert-Butylimino)-N,N-diethyl-1,3-diméthyl-1,3,2l5… …N,N-diisopropylcarbodiimide DIEA N,N-diisopropyléthylamine DMF N,N-diméthylformamide… …nanomolaire NMM N-méthylmorpholine NMP N-méthyl-2-pyrrolidone NMR Nuclear Magnetic Resonance… …thérapeutiques. Par exemple la ghréline (1.1) 3 est un peptide N-acylé (Figure 1.1… 

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APA (6th Edition):

Chignen Possi, K. (2018). Synthèse des analogues de l’[azaPhe4]-GHRP-6 comme potentiels modulateurs du récepteur CD36. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/20037

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chignen Possi, Kelvine. “Synthèse des analogues de l’[azaPhe4]-GHRP-6 comme potentiels modulateurs du récepteur CD36.” 2018. Thesis, Université de Montréal. Accessed April 16, 2021. http://hdl.handle.net/1866/20037.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chignen Possi, Kelvine. “Synthèse des analogues de l’[azaPhe4]-GHRP-6 comme potentiels modulateurs du récepteur CD36.” 2018. Web. 16 Apr 2021.

Vancouver:

Chignen Possi K. Synthèse des analogues de l’[azaPhe4]-GHRP-6 comme potentiels modulateurs du récepteur CD36. [Internet] [Thesis]. Université de Montréal; 2018. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1866/20037.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chignen Possi K. Synthèse des analogues de l’[azaPhe4]-GHRP-6 comme potentiels modulateurs du récepteur CD36. [Thesis]. Université de Montréal; 2018. Available from: http://hdl.handle.net/1866/20037

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Montréal

29. Savoie, Jolaine. Développement d'une méthode d'alkylation pour la préparation de ligands carbènes N-hétérocycliques C₁-symétriques et synthèse de nouveaux catalyseurs pour la métathèse d'oléfines.

Degree: 2009, Université de Montréal

Subjects/Keywords: Carbène N-hétérocyclique (NHC); Alkylation; Catalyse asymétrique; Métathèse d'oléfine par fermeture de cycle (RCM); N-heterocyclic ligands (NHC); Alkylation; Cyclic aminals; Asymmetric catalyst; Assymetric ring-closing metathesis (RCM)

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APA (6th Edition):

Savoie, J. (2009). Développement d'une méthode d'alkylation pour la préparation de ligands carbènes N-hétérocycliques C₁-symétriques et synthèse de nouveaux catalyseurs pour la métathèse d'oléfines. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/7829

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Savoie, Jolaine. “Développement d'une méthode d'alkylation pour la préparation de ligands carbènes N-hétérocycliques C₁-symétriques et synthèse de nouveaux catalyseurs pour la métathèse d'oléfines.” 2009. Thesis, Université de Montréal. Accessed April 16, 2021. http://hdl.handle.net/1866/7829.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Savoie, Jolaine. “Développement d'une méthode d'alkylation pour la préparation de ligands carbènes N-hétérocycliques C₁-symétriques et synthèse de nouveaux catalyseurs pour la métathèse d'oléfines.” 2009. Web. 16 Apr 2021.

Vancouver:

Savoie J. Développement d'une méthode d'alkylation pour la préparation de ligands carbènes N-hétérocycliques C₁-symétriques et synthèse de nouveaux catalyseurs pour la métathèse d'oléfines. [Internet] [Thesis]. Université de Montréal; 2009. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1866/7829.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Savoie J. Développement d'une méthode d'alkylation pour la préparation de ligands carbènes N-hétérocycliques C₁-symétriques et synthèse de nouveaux catalyseurs pour la métathèse d'oléfines. [Thesis]. Université de Montréal; 2009. Available from: http://hdl.handle.net/1866/7829

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Montréal

30. Holtz-Mulholland, Michael. Synthesis of transition metal N-heterocyclic carbene complexes and applications in catalysis.

Degree: 2015, Université de Montréal

Subjects/Keywords: NHC; C1-symmétrique; Carbène N-hétérocyclique; Relais chiral; Alkylation; Cuivre; Or; Couplage oxydatif; BINOL; Binaphthyl; N-Heterocyclic Carbene; NHC; Chiral Relay; C1-symmetric; Alkylation; Copper; Gold; Oxidative Coupling; BINOL; Binaphthyl; Chemistry - Organic / Chimie organique (UMI : 0490)

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APA (6th Edition):

Holtz-Mulholland, M. (2015). Synthesis of transition metal N-heterocyclic carbene complexes and applications in catalysis. (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/11407

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Holtz-Mulholland, Michael. “Synthesis of transition metal N-heterocyclic carbene complexes and applications in catalysis.” 2015. Thesis, Université de Montréal. Accessed April 16, 2021. http://hdl.handle.net/1866/11407.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Holtz-Mulholland, Michael. “Synthesis of transition metal N-heterocyclic carbene complexes and applications in catalysis.” 2015. Web. 16 Apr 2021.

Vancouver:

Holtz-Mulholland M. Synthesis of transition metal N-heterocyclic carbene complexes and applications in catalysis. [Internet] [Thesis]. Université de Montréal; 2015. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1866/11407.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Holtz-Mulholland M. Synthesis of transition metal N-heterocyclic carbene complexes and applications in catalysis. [Thesis]. Université de Montréal; 2015. Available from: http://hdl.handle.net/1866/11407

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

[1] [2]

.