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You searched for subject:(N alkylation). Showing records 1 – 25 of 25 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 19, 2019. 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. 19 Apr 2019.

Vancouver:

Kholod Zaitseva I. New approaches for the synthesis of advanced precursors of Rhazinilam analogues. [Internet] [Thesis]. Université de Neuchâtel; 2014. [cited 2019 Apr 19]. 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


Université Montpellier II

2. 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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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


Université Catholique de Louvain

3. Van Den Berge, Emilie. Development of a general and regioselective N-alkylation strategy of azoles and synthesis of original imidazole derivatives of chemical and biological interest.

Degree: 2013, Université Catholique de Louvain

Imidazoles are key structures in medicinal chemistry. Numbers of imidazole derivatives have found applications in the treatment of infectious diseases, cancer, metabolic, cardiovascular, and CNS… (more)

Subjects/Keywords: imidazole; macrocycles; antitumor activity; chirality; regioselective N-alkylation

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APA (6th Edition):

Van Den Berge, E. (2013). Development of a general and regioselective N-alkylation strategy of azoles and synthesis of original imidazole derivatives of chemical and biological interest. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/134459

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):

Van Den Berge, Emilie. “Development of a general and regioselective N-alkylation strategy of azoles and synthesis of original imidazole derivatives of chemical and biological interest.” 2013. Thesis, Université Catholique de Louvain. Accessed April 19, 2019. http://hdl.handle.net/2078.1/134459.

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

MLA Handbook (7th Edition):

Van Den Berge, Emilie. “Development of a general and regioselective N-alkylation strategy of azoles and synthesis of original imidazole derivatives of chemical and biological interest.” 2013. Web. 19 Apr 2019.

Vancouver:

Van Den Berge E. Development of a general and regioselective N-alkylation strategy of azoles and synthesis of original imidazole derivatives of chemical and biological interest. [Internet] [Thesis]. Université Catholique de Louvain; 2013. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/2078.1/134459.

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

Council of Science Editors:

Van Den Berge E. Development of a general and regioselective N-alkylation strategy of azoles and synthesis of original imidazole derivatives of chemical and biological interest. [Thesis]. Université Catholique de Louvain; 2013. Available from: http://hdl.handle.net/2078.1/134459

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


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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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://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 19, 2019. 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. 19 Apr 2019.

Vancouver:

Al Badran F. Reactor design : compact and catalytic for speciality chemicals. [Internet] [Doctoral dissertation]. University of Bath; 2011. [cited 2019 Apr 19]. Available from: 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://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.545331


University of New Orleans

6. 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 19, 2019. 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. 19 Apr 2019.

Vancouver:

Lindsay M. Studies directed Towards the Iridium Catalyzed Synthesis of New Carbon-Nitrogen Bonds. [Internet] [Doctoral dissertation]. University of New Orleans; 2017. [cited 2019 Apr 19]. 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


Universidade Federal de Santa Maria

7. 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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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


Université de Montréal

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

Degree: 2015, Université de Montréal

 Les ligands de carbènes N-hétérocycliques (NHC) qui possèdent une symétrie C1 attirent beaucoup l’attention dans la littérature. Le présent projet de recherche propose de synthétiser… (more)

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

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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 19, 2019. 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. 19 Apr 2019.

Vancouver:

Holtz-Mulholland M. Synthesis of transition metal N-heterocyclic carbene complexes and applications in catalysis . [Internet] [Thesis]. Université de Montréal; 2015. [cited 2019 Apr 19]. 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


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 19, 2019. 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. 19 Apr 2019.

Vancouver:

Bajaber MA. Study of Iridium Catalyzed N-Alkylation of Urea with Benzyl Alcohols. [Internet] [Thesis]. University of New Orleans; 2014. [cited 2019 Apr 19]. 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


University of New Orleans

10. 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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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


Brno University of Technology

11. Cigánek, Martin. Syntéza a studium nových derivátů diketopyrrolopyrrolů (DPPs) pro organickou elektroniku .

Degree: 2017, Brno University of Technology

 Předkládaná diplomová práce pojednává o organických pigmentech diketopyrrolopyrrolech (DPPs), které disponují vlastnostmi uplatnitelnými v atraktivních a perspektivních oblastech organické elektroniky a fotoniky. Provedena byla modifikace… (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. (2017). Syntéza a studium nových derivátů diketopyrrolopyrrolů (DPPs) pro organickou elektroniku . (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 .” 2017. Thesis, Brno University of Technology. Accessed April 19, 2019. 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 .” 2017. Web. 19 Apr 2019.

Vancouver:

Cigánek M. Syntéza a studium nových derivátů diketopyrrolopyrrolů (DPPs) pro organickou elektroniku . [Internet] [Thesis]. Brno University of Technology; 2017. [cited 2019 Apr 19]. 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 . [Thesis]. Brno University of Technology; 2017. 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

12. 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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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

13. 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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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


University of Bath

14. 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://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 19, 2019. 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. 19 Apr 2019.

Vancouver:

Hamid MHSA. Conversion of alcohols into amines by borrowing hydrogen. [Internet] [Doctoral dissertation]. University of Bath; 2008. [cited 2019 Apr 19]. Available from: 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://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501635

15. 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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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

16. 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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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


Université de Montréal

17. 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

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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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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

18. Turcotte, Stéphane. Les azasulfurylpeptides : synthèse, analyse conformationnelle et applications biologiques .

Degree: 2015, Université de Montréal

 Les azasulfurylpeptides sont des mimes peptidiques auxquels le carbone en position alpha et le carbonyle d’un acide aminé sont respectivement remplacés par un atome d’azote… (more)

Subjects/Keywords: Mimes peptidiques; Azasulfurylpeptides; N-Aminosulfamides; Alkylation chimio-sélective; GHRP-6; TLR2; Régulation des réponses inflammatoires et immunitaires innées; Inhibiteurs de métallo-bêta-lactamases; Peptide mimicry; Chemoselective alkylation; CD36; Regulation of innate immunity and inflammatory responses; Metallo-bêta-lactamases inhibitors

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APA (6th Edition):

Turcotte, S. (2015). Les azasulfurylpeptides : synthèse, analyse conformationnelle et applications biologiques . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/12321

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):

Turcotte, Stéphane. “Les azasulfurylpeptides : synthèse, analyse conformationnelle et applications biologiques .” 2015. Thesis, Université de Montréal. Accessed April 19, 2019. http://hdl.handle.net/1866/12321.

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

MLA Handbook (7th Edition):

Turcotte, Stéphane. “Les azasulfurylpeptides : synthèse, analyse conformationnelle et applications biologiques .” 2015. Web. 19 Apr 2019.

Vancouver:

Turcotte S. Les azasulfurylpeptides : synthèse, analyse conformationnelle et applications biologiques . [Internet] [Thesis]. Université de Montréal; 2015. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1866/12321.

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

Council of Science Editors:

Turcotte S. Les azasulfurylpeptides : synthèse, analyse conformationnelle et applications biologiques . [Thesis]. Université de Montréal; 2015. Available from: http://hdl.handle.net/1866/12321

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


Université de Montréal

19. Proulx, Caroline. Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36 .

Degree: 2012, Université de Montréal

 Les azapeptides sont des mimes peptidiques où le carbone alpha d’un ou de plusieurs acides aminés est remplacé par un atome d’azote. Cette modification tend… (more)

Subjects/Keywords: Azapeptides; Repliement beta; Mimes peptidiques; GHRP-6; Récepteur GHS-R1a; Récepteur CD36; Angiogénèse; Semicarbazone; N-Alkylation; N-Arylation; Aza-propargylglycine; Cycloaddition 1,3-dipolaire; Couplage A3; N-amino-imidazolin-2-ones; Beta turn; Peptide mimicry; GHS-R1a receptor; CD36 receptor; Angiogenesis; 1,3-Dipolar cycloaddition; A3 coupling

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APA (6th Edition):

Proulx, C. (2012). Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36 . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/8887

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):

Proulx, Caroline. “Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36 .” 2012. Thesis, Université de Montréal. Accessed April 19, 2019. http://hdl.handle.net/1866/8887.

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

MLA Handbook (7th Edition):

Proulx, Caroline. “Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36 .” 2012. Web. 19 Apr 2019.

Vancouver:

Proulx C. Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36 . [Internet] [Thesis]. Université de Montréal; 2012. [cited 2019 Apr 19]. Available from: http://hdl.handle.net/1866/8887.

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

Council of Science Editors:

Proulx C. Méthodologie pour la synthèse combinatoire d’azapeptides: application à la synthèse d’analogues aza-GHRP-6 en tant que ligands du récepteur CD36 . [Thesis]. Université de Montréal; 2012. Available from: http://hdl.handle.net/1866/8887

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

20. 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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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


Kyoto University / 京都大学

21. 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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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

22. 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 19, 2019. 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. 19 Apr 2019.

Vancouver:

Chang Y. Studies on PNP-Pincer Type Phosphaalkene Complexes of Iridium . [Internet] [Thesis]. Kyoto University; 2014. [cited 2019 Apr 19]. 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


University of Vienna

23. Deckardt, Sophie Katharina. Strukturelle Modifikation des Alkaloids Luotonin A.

Degree: 2017, University of Vienna

 Im Rahmen dieser Diplomarbeit konnte erfolgreich ein bisher unzugängliches 2-Hydroxy-ethyl-Derivat des zytotoxischen Naturstoffs Luotonin A hergestellt werden. Als Syntheseweg hierfür wurde die von unserer Arbeitsgruppe… (more)

Subjects/Keywords: 35.59 Heterocyclische Verbindungen; 35.07 Chemisches Labor, chemische Methoden; Luotonin A / Topoisomerasehemmer / Hydroxyethyl-Seitenkette / Weinreb-Amidierung / N-Alkylierung / aza-Diels-Alder-Reaktion; Luotonin A / topoisomerase inhibitor / hydroxyethyl side chain / weinreb amidation / N-alkylation / aza-Diels-Alder reaction

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

APA (6th Edition):

Deckardt, S. K. (2017). Strukturelle Modifikation des Alkaloids Luotonin A. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/48232/

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):

Deckardt, Sophie Katharina. “Strukturelle Modifikation des Alkaloids Luotonin A.” 2017. Thesis, University of Vienna. Accessed April 19, 2019. http://othes.univie.ac.at/48232/.

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

MLA Handbook (7th Edition):

Deckardt, Sophie Katharina. “Strukturelle Modifikation des Alkaloids Luotonin A.” 2017. Web. 19 Apr 2019.

Vancouver:

Deckardt SK. Strukturelle Modifikation des Alkaloids Luotonin A. [Internet] [Thesis]. University of Vienna; 2017. [cited 2019 Apr 19]. Available from: http://othes.univie.ac.at/48232/.

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

Council of Science Editors:

Deckardt SK. Strukturelle Modifikation des Alkaloids Luotonin A. [Thesis]. University of Vienna; 2017. Available from: http://othes.univie.ac.at/48232/

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


Université de Montréal

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

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 19, 2019. 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. 19 Apr 2019.

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 2019 Apr 19]. 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

25. Clay, Charles Michael. Synthesis of Isatin Derivatives Used for the Inhibition of Pro-Apoptotic Jurkat T Cells.

Degree: MS, Chemistry, 2011, Wright State University

 A range of substituted 1H-indole-2,3-diones (isatins) was synthesized to assess their capability to inhibit caspases and prevent apoptosis in Jurkat T cells. The key steps… (more)

Subjects/Keywords: Chemistry; Isatin; Oxindole; Benzylidene; N-alkylation; Knoevenagel condensation; Wolff-Kishner reduction; Apoptosis; Caspases; Caspase inhibitor; small molecule inhibitor; Biological Screening; DNA laddering; Q-VD-OPh

…77 vi LIST OF TABLES Page Table 1- Reported Solvents and Bases used for the N-Alkylation… …Irradiation ….…..38 Table 3- N-Alkylation of Isatin via Microwave Irradiation …. 39 Table 4… …N-Alkylation of Isatin via Conventional Heating ….. .42 Table 5- N-Alkylation of 5… …O SiO2 N X CH2Cl2, rt. S N O O H X = Cl, Br, I O 37 36 N-Alkylation of Isatin… …N-alkylation of isatin proceeds by reacting the isatin (32) substrate with any… 

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

APA (6th Edition):

Clay, C. M. (2011). Synthesis of Isatin Derivatives Used for the Inhibition of Pro-Apoptotic Jurkat T Cells. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1315518391

Chicago Manual of Style (16th Edition):

Clay, Charles Michael. “Synthesis of Isatin Derivatives Used for the Inhibition of Pro-Apoptotic Jurkat T Cells.” 2011. Masters Thesis, Wright State University. Accessed April 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1315518391.

MLA Handbook (7th Edition):

Clay, Charles Michael. “Synthesis of Isatin Derivatives Used for the Inhibition of Pro-Apoptotic Jurkat T Cells.” 2011. Web. 19 Apr 2019.

Vancouver:

Clay CM. Synthesis of Isatin Derivatives Used for the Inhibition of Pro-Apoptotic Jurkat T Cells. [Internet] [Masters thesis]. Wright State University; 2011. [cited 2019 Apr 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1315518391.

Council of Science Editors:

Clay CM. Synthesis of Isatin Derivatives Used for the Inhibition of Pro-Apoptotic Jurkat T Cells. [Masters Thesis]. Wright State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1315518391

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