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You searched for subject:(Oxazolidinones). Showing records 1 – 12 of 12 total matches.

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1. Simão, Ana Catarina. Ancrages sélectifs sur cétohexoses de thionocarbamates cycliques : Selective anchoring of cyclic thionocarbamates on ketohexoses.

Degree: Docteur es, Chimie organique, 2009, Orléans; Université de Lisbonne

Une réaction simple de condensation de l'acide thiocyanique avec un cétohexose peut conduire à la formation d’une dizaine de 10 oxazolidinethiones (OZTs) ou oxazolinethiones (OXTs)… (more)

Subjects/Keywords: Oxazolidinethiones; Oxazolidinones; Cétohexoses; D-fructose; D-psicose; D-tagatose; Thionocarbamates; Oxazolidinethiones; Oxazolidinones; Ketohexoses; D-fructose; D-psicose; D-tagatose; Thionocarbamates

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APA (6th Edition):

Simão, A. C. (2009). Ancrages sélectifs sur cétohexoses de thionocarbamates cycliques : Selective anchoring of cyclic thionocarbamates on ketohexoses. (Doctoral Dissertation). Orléans; Université de Lisbonne. Retrieved from http://www.theses.fr/2009ORLE2038

Chicago Manual of Style (16th Edition):

Simão, Ana Catarina. “Ancrages sélectifs sur cétohexoses de thionocarbamates cycliques : Selective anchoring of cyclic thionocarbamates on ketohexoses.” 2009. Doctoral Dissertation, Orléans; Université de Lisbonne. Accessed December 09, 2019. http://www.theses.fr/2009ORLE2038.

MLA Handbook (7th Edition):

Simão, Ana Catarina. “Ancrages sélectifs sur cétohexoses de thionocarbamates cycliques : Selective anchoring of cyclic thionocarbamates on ketohexoses.” 2009. Web. 09 Dec 2019.

Vancouver:

Simão AC. Ancrages sélectifs sur cétohexoses de thionocarbamates cycliques : Selective anchoring of cyclic thionocarbamates on ketohexoses. [Internet] [Doctoral dissertation]. Orléans; Université de Lisbonne; 2009. [cited 2019 Dec 09]. Available from: http://www.theses.fr/2009ORLE2038.

Council of Science Editors:

Simão AC. Ancrages sélectifs sur cétohexoses de thionocarbamates cycliques : Selective anchoring of cyclic thionocarbamates on ketohexoses. [Doctoral Dissertation]. Orléans; Université de Lisbonne; 2009. Available from: http://www.theses.fr/2009ORLE2038


University of Bath

2. Ho, Hoi Tong Lawrence. New methods in chiral synthesis.

Degree: PhD, 1999, University of Bath

Subjects/Keywords: 547; Solid phase; Oxazolidinones

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APA (6th Edition):

Ho, H. T. L. (1999). New methods in chiral synthesis. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/new-methods-in-chiral-synthesis(cbd07455-8466-43f4-95a6-9c472ddfc44f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301557

Chicago Manual of Style (16th Edition):

Ho, Hoi Tong Lawrence. “New methods in chiral synthesis.” 1999. Doctoral Dissertation, University of Bath. Accessed December 09, 2019. https://researchportal.bath.ac.uk/en/studentthesis/new-methods-in-chiral-synthesis(cbd07455-8466-43f4-95a6-9c472ddfc44f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301557.

MLA Handbook (7th Edition):

Ho, Hoi Tong Lawrence. “New methods in chiral synthesis.” 1999. Web. 09 Dec 2019.

Vancouver:

Ho HTL. New methods in chiral synthesis. [Internet] [Doctoral dissertation]. University of Bath; 1999. [cited 2019 Dec 09]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/new-methods-in-chiral-synthesis(cbd07455-8466-43f4-95a6-9c472ddfc44f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301557.

Council of Science Editors:

Ho HTL. New methods in chiral synthesis. [Doctoral Dissertation]. University of Bath; 1999. Available from: https://researchportal.bath.ac.uk/en/studentthesis/new-methods-in-chiral-synthesis(cbd07455-8466-43f4-95a6-9c472ddfc44f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.301557

3. Zheng, Zilong. Synthesis of Oxazolidinone Derivatives and Anti-Influenza Agents.

Degree: PhD, Chemistry and Biochemistry (Arts and Sciences), 2016, Ohio University

Oxazolidinones Derivatives are useful compounds in both synthetic chemistry and biochemistry. The addition reaction of fused ring aziridine and halides was developed, which provide a… (more)

Subjects/Keywords: Chemistry; Oxazolidinones; aziridine; anti-influenza

…25 Scheme 2.3: Synthesis of fused-ring oxazolidinones… …91 13 CHAPTER 1: INTRODUCTION TO OXAZOLIDINONE 2-Oxazolidinones are a type of… …prepare oxazolidinones. (Table 1.1, entry 2-5) Urea could also be used to introduce… …oxazolidinones, which work by binding to 23S ribosomal RNA and inhibit the translation at the… …oxazolidinones are able to bind two structurally related T box antiterminator model RNAs. For example… 

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APA (6th Edition):

Zheng, Z. (2016). Synthesis of Oxazolidinone Derivatives and Anti-Influenza Agents. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1470739369

Chicago Manual of Style (16th Edition):

Zheng, Zilong. “Synthesis of Oxazolidinone Derivatives and Anti-Influenza Agents.” 2016. Doctoral Dissertation, Ohio University. Accessed December 09, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1470739369.

MLA Handbook (7th Edition):

Zheng, Zilong. “Synthesis of Oxazolidinone Derivatives and Anti-Influenza Agents.” 2016. Web. 09 Dec 2019.

Vancouver:

Zheng Z. Synthesis of Oxazolidinone Derivatives and Anti-Influenza Agents. [Internet] [Doctoral dissertation]. Ohio University; 2016. [cited 2019 Dec 09]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1470739369.

Council of Science Editors:

Zheng Z. Synthesis of Oxazolidinone Derivatives and Anti-Influenza Agents. [Doctoral Dissertation]. Ohio University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1470739369


University of Cincinnati

4. HANCOCK, MATTHEW THOMAS. THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES.

Degree: PhD, Arts and Sciences : Chemistry, 2003, University of Cincinnati

 Several novel transformations of aziridines to 1,2-diamines, 2-oxazolidinones, and benzodiazepines have been developed. Previous work in the Pinhas group showed that an aziridine could be… (more)

Subjects/Keywords: Chemistry, Organic; aziridines; diamines; oxazolidinones; benzodiazepines; carbon dioxide insertion

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APA (6th Edition):

HANCOCK, M. T. (2003). THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1054137190

Chicago Manual of Style (16th Edition):

HANCOCK, MATTHEW THOMAS. “THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES.” 2003. Doctoral Dissertation, University of Cincinnati. Accessed December 09, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1054137190.

MLA Handbook (7th Edition):

HANCOCK, MATTHEW THOMAS. “THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES.” 2003. Web. 09 Dec 2019.

Vancouver:

HANCOCK MT. THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES. [Internet] [Doctoral dissertation]. University of Cincinnati; 2003. [cited 2019 Dec 09]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1054137190.

Council of Science Editors:

HANCOCK MT. THE DEVELOPMENT OF NOVEL AND CONVENIENT TRANSFORMATIONS OF AZIRIDINES. [Doctoral Dissertation]. University of Cincinnati; 2003. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1054137190

5. D.M. Carminati. METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS.

Degree: 2018, Università degli Studi di Milano

 Cyclopropanes and nitrogen-containing compounds, such as aziridines, indoles and amines, are interesting molecules from a synthetic point of view because they are often used as… (more)

Subjects/Keywords: porphyrin; metal porphyrin complexes; catalysis; cyclopropanes; aziridines; oxazolidinones; indoles; amines; Settore CHIM/03 - Chimica Generale e Inorganica

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APA (6th Edition):

Carminati, D. (2018). METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/541869

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):

Carminati, D.M.. “METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS.” 2018. Thesis, Università degli Studi di Milano. Accessed December 09, 2019. http://hdl.handle.net/2434/541869.

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

MLA Handbook (7th Edition):

Carminati, D.M.. “METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS.” 2018. Web. 09 Dec 2019.

Vancouver:

Carminati D. METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS. [Internet] [Thesis]. Università degli Studi di Milano; 2018. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2434/541869.

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

Council of Science Editors:

Carminati D. METAL PORPHYRIN COMPLEXES: SMART CATALYSTS TO PROMOTE ECO-FRIENDLY C-C AND C-N BOND FORMATIONS. [Thesis]. Università degli Studi di Milano; 2018. Available from: http://hdl.handle.net/2434/541869

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


University of Florida

6. Sahre, Martina. Pharmacokinetic/Pharmacodynamic Characterization of TR-700 (Torezolid).

Degree: PhD, Pharmaceutical Sciences - Pharmaceutics, 2010, University of Florida

 Infections with methicillin-resistant Staphylococcus aureus (MRSA) have become endemic in healthcare settings around the world and recently patients without risk-factors have become infected in the… (more)

Subjects/Keywords: Adipose tissues; Calibration; Dosage; Infections; Muscle tissues; Oxazolidinones; Pharmacokinetics; Plasmas; Quality assurance; Tissue samples; antibiotics, distribution, microdialysis, pharmacodynamics, pharmacokinetics, tissue, torezolid

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APA (6th Edition):

Sahre, M. (2010). Pharmacokinetic/Pharmacodynamic Characterization of TR-700 (Torezolid). (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042485

Chicago Manual of Style (16th Edition):

Sahre, Martina. “Pharmacokinetic/Pharmacodynamic Characterization of TR-700 (Torezolid).” 2010. Doctoral Dissertation, University of Florida. Accessed December 09, 2019. http://ufdc.ufl.edu/UFE0042485.

MLA Handbook (7th Edition):

Sahre, Martina. “Pharmacokinetic/Pharmacodynamic Characterization of TR-700 (Torezolid).” 2010. Web. 09 Dec 2019.

Vancouver:

Sahre M. Pharmacokinetic/Pharmacodynamic Characterization of TR-700 (Torezolid). [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 Dec 09]. Available from: http://ufdc.ufl.edu/UFE0042485.

Council of Science Editors:

Sahre M. Pharmacokinetic/Pharmacodynamic Characterization of TR-700 (Torezolid). [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0042485

7. Orac, Crina M. Stereochemical Synthesis of Ring E Analogs of Methyllycaconitine and 4,5-Disubstituted Oxazolidinones.

Degree: PhD, Chemistry and Biochemistry (Arts and Sciences), 2009, Ohio University

  The pharmacological activity of enantiomers of a chiral compound can be influenced to a great extent by molecular chiral recognition, the ability of a… (more)

Subjects/Keywords: Organic Chemistry; nicotinic; acetylcholine; methyllycaconitine; enantiomers; antibiotics; antiterminator; oxazolidinones

Oxazolidinones A dissertation presented to the faculty of the College of Arts and Sciences of Ohio… …Stereochemical Synthesis of Ring E Analogs of Methyllycaconitine and 4,5-Disubstituted Oxazolidinones… …Analogs of Methyllycaconitine and 4,5-Disubstituted Oxazolidinones (320 pp.) Director… …disubstituted oxazolidinones in an effort to understand their interaction with their biological… …oxazolidinones, has been developed that exhibit inhibitory activity at the T box transcription… 

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APA (6th Edition):

Orac, C. M. (2009). Stereochemical Synthesis of Ring E Analogs of Methyllycaconitine and 4,5-Disubstituted Oxazolidinones. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1258046479

Chicago Manual of Style (16th Edition):

Orac, Crina M. “Stereochemical Synthesis of Ring E Analogs of Methyllycaconitine and 4,5-Disubstituted Oxazolidinones.” 2009. Doctoral Dissertation, Ohio University. Accessed December 09, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1258046479.

MLA Handbook (7th Edition):

Orac, Crina M. “Stereochemical Synthesis of Ring E Analogs of Methyllycaconitine and 4,5-Disubstituted Oxazolidinones.” 2009. Web. 09 Dec 2019.

Vancouver:

Orac CM. Stereochemical Synthesis of Ring E Analogs of Methyllycaconitine and 4,5-Disubstituted Oxazolidinones. [Internet] [Doctoral dissertation]. Ohio University; 2009. [cited 2019 Dec 09]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1258046479.

Council of Science Editors:

Orac CM. Stereochemical Synthesis of Ring E Analogs of Methyllycaconitine and 4,5-Disubstituted Oxazolidinones. [Doctoral Dissertation]. Ohio University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1258046479


University of Manitoba

8. Hein, Jason Ellis. Tools for efficient asymmetric synthesis: design, synthesis and application of fluorous oxazolidinone chiral auxiliaries.

Degree: Chemistry, 2006, University of Manitoba

 A new class of oxazolidinone chiral auxiliary has been synthesized from various α-amino acids, incorporating a perfluoroalkyl functional chain as a soluble support. This feature… (more)

Subjects/Keywords: Fluorous chiral auxiliary; asymmetric synthesis; organic chemistry; oxazolidinones; aldol reactions

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APA (6th Edition):

Hein, J. E. (2006). Tools for efficient asymmetric synthesis: design, synthesis and application of fluorous oxazolidinone chiral auxiliaries. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/187

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):

Hein, Jason Ellis. “Tools for efficient asymmetric synthesis: design, synthesis and application of fluorous oxazolidinone chiral auxiliaries.” 2006. Thesis, University of Manitoba. Accessed December 09, 2019. http://hdl.handle.net/1993/187.

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

MLA Handbook (7th Edition):

Hein, Jason Ellis. “Tools for efficient asymmetric synthesis: design, synthesis and application of fluorous oxazolidinone chiral auxiliaries.” 2006. Web. 09 Dec 2019.

Vancouver:

Hein JE. Tools for efficient asymmetric synthesis: design, synthesis and application of fluorous oxazolidinone chiral auxiliaries. [Internet] [Thesis]. University of Manitoba; 2006. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1993/187.

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

Council of Science Editors:

Hein JE. Tools for efficient asymmetric synthesis: design, synthesis and application of fluorous oxazolidinone chiral auxiliaries. [Thesis]. University of Manitoba; 2006. Available from: http://hdl.handle.net/1993/187

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

9. Acquaah-Harrison, George. Antibacterial Agents: 1,4-Disubstituted 1,2,3-Triazole Analogs of the Oxazolidinone.

Degree: PhD, Chemistry and Biochemistry (Arts and Sciences), 2010, Ohio University

  The rational design, development and synthesis of structurally diverse small molecule that target RNA is immensely important in antibacterial therapy. Utilizing rational design approach… (more)

Subjects/Keywords: Chemistry; Antibacterial agents; Bioisosteric replacement; Analogs of oxazolidinones; RNA binding ligands

…these oxazolidinones bind RNA without significant dependence on electrostatic interactions but… …with enhanced biological activity.81,82 These lead oxazolidinones were also found to bind to… …their topological identity relative to the oxazolidinones. While biological evaluation of… 

Page 1 Page 2 Page 3 Page 4 Page 5

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APA (6th Edition):

Acquaah-Harrison, G. (2010). Antibacterial Agents: 1,4-Disubstituted 1,2,3-Triazole Analogs of the Oxazolidinone. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1273250347

Chicago Manual of Style (16th Edition):

Acquaah-Harrison, George. “Antibacterial Agents: 1,4-Disubstituted 1,2,3-Triazole Analogs of the Oxazolidinone.” 2010. Doctoral Dissertation, Ohio University. Accessed December 09, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1273250347.

MLA Handbook (7th Edition):

Acquaah-Harrison, George. “Antibacterial Agents: 1,4-Disubstituted 1,2,3-Triazole Analogs of the Oxazolidinone.” 2010. Web. 09 Dec 2019.

Vancouver:

Acquaah-Harrison G. Antibacterial Agents: 1,4-Disubstituted 1,2,3-Triazole Analogs of the Oxazolidinone. [Internet] [Doctoral dissertation]. Ohio University; 2010. [cited 2019 Dec 09]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1273250347.

Council of Science Editors:

Acquaah-Harrison G. Antibacterial Agents: 1,4-Disubstituted 1,2,3-Triazole Analogs of the Oxazolidinone. [Doctoral Dissertation]. Ohio University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1273250347


Université de Montréal

10. Huard, Kim. Les N-tosyloxycarbamates : une nouvelle source de nitrènes métalliques pour la réaction d'insertion de liens carbone-hydrogène .

Degree: 2008, Université de Montréal

Subjects/Keywords: N-tosyloxycarbamates; Dimères de rhodium; Amination; Nitrènes métalliques; Insertion de liens C-H; Oxazolidinones

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APA (6th Edition):

Huard, K. (2008). Les N-tosyloxycarbamates : une nouvelle source de nitrènes métalliques pour la réaction d'insertion de liens carbone-hydrogène . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6549

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):

Huard, Kim. “Les N-tosyloxycarbamates : une nouvelle source de nitrènes métalliques pour la réaction d'insertion de liens carbone-hydrogène .” 2008. Thesis, Université de Montréal. Accessed December 09, 2019. http://hdl.handle.net/1866/6549.

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

MLA Handbook (7th Edition):

Huard, Kim. “Les N-tosyloxycarbamates : une nouvelle source de nitrènes métalliques pour la réaction d'insertion de liens carbone-hydrogène .” 2008. Web. 09 Dec 2019.

Vancouver:

Huard K. Les N-tosyloxycarbamates : une nouvelle source de nitrènes métalliques pour la réaction d'insertion de liens carbone-hydrogène . [Internet] [Thesis]. Université de Montréal; 2008. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1866/6549.

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

Council of Science Editors:

Huard K. Les N-tosyloxycarbamates : une nouvelle source de nitrènes métalliques pour la réaction d'insertion de liens carbone-hydrogène . [Thesis]. Université de Montréal; 2008. Available from: http://hdl.handle.net/1866/6549

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


University of New Orleans

11. Ella-Menye, Jean-Rene. Synthesis of Novel Chiral Heterocyclic Compounds for Antibacterial Agents and Peptidomimetics.

Degree: PhD, Chemistry, 2007, University of New Orleans

 Small chiral molecules are very important building blocks in the synthesis of biologically active compounds. These building blocks include nitrogen and oxygen-containing heterocycles such as… (more)

Subjects/Keywords: Chiral heterocycles; 2-oxazolidinones; 1; 3-oxazinan-2-ones; aeruginosins; 2-carboxy-6-hydroxyoctahydroindole; serine protease inhibitors.

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APA (6th Edition):

Ella-Menye, J. (2007). Synthesis of Novel Chiral Heterocyclic Compounds for Antibacterial Agents and Peptidomimetics. (Doctoral Dissertation). University of New Orleans. Retrieved from https://scholarworks.uno.edu/td/611

Chicago Manual of Style (16th Edition):

Ella-Menye, Jean-Rene. “Synthesis of Novel Chiral Heterocyclic Compounds for Antibacterial Agents and Peptidomimetics.” 2007. Doctoral Dissertation, University of New Orleans. Accessed December 09, 2019. https://scholarworks.uno.edu/td/611.

MLA Handbook (7th Edition):

Ella-Menye, Jean-Rene. “Synthesis of Novel Chiral Heterocyclic Compounds for Antibacterial Agents and Peptidomimetics.” 2007. Web. 09 Dec 2019.

Vancouver:

Ella-Menye J. Synthesis of Novel Chiral Heterocyclic Compounds for Antibacterial Agents and Peptidomimetics. [Internet] [Doctoral dissertation]. University of New Orleans; 2007. [cited 2019 Dec 09]. Available from: https://scholarworks.uno.edu/td/611.

Council of Science Editors:

Ella-Menye J. Synthesis of Novel Chiral Heterocyclic Compounds for Antibacterial Agents and Peptidomimetics. [Doctoral Dissertation]. University of New Orleans; 2007. Available from: https://scholarworks.uno.edu/td/611

12. Mamani Laparra, Laura. Réaction d’amination intramoléculaire de liens C-H à partir de N-mésyloxycarbamates catalysée par des complexes de rhodium et d’autres métaux de transition : s ynthèse verte d’oxazolidinones .

Degree: 2016, Université de Montréal

 La réaction d’amination de liens C-H, impliquant la transformation directe d’un lien C-H en lien C-N constitue une approche synthétique d’avenir pour la préparation de… (more)

Subjects/Keywords: Amination de liens C-H; N-Mésyloxycarbamates; Oxazolidinones; Dimères de rhodium; Phtalocyanine de fer; Pinceurs de nickel; C-H Amination; N-Mesyloxycarbamates; Rhodium dimers; Iron phtalocyanin; Nickel pincers

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APA (6th Edition):

Mamani Laparra, L. (2016). Réaction d’amination intramoléculaire de liens C-H à partir de N-mésyloxycarbamates catalysée par des complexes de rhodium et d’autres métaux de transition : s ynthèse verte d’oxazolidinones . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/13960

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):

Mamani Laparra, Laura. “Réaction d’amination intramoléculaire de liens C-H à partir de N-mésyloxycarbamates catalysée par des complexes de rhodium et d’autres métaux de transition : s ynthèse verte d’oxazolidinones .” 2016. Thesis, Université de Montréal. Accessed December 09, 2019. http://hdl.handle.net/1866/13960.

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

MLA Handbook (7th Edition):

Mamani Laparra, Laura. “Réaction d’amination intramoléculaire de liens C-H à partir de N-mésyloxycarbamates catalysée par des complexes de rhodium et d’autres métaux de transition : s ynthèse verte d’oxazolidinones .” 2016. Web. 09 Dec 2019.

Vancouver:

Mamani Laparra L. Réaction d’amination intramoléculaire de liens C-H à partir de N-mésyloxycarbamates catalysée par des complexes de rhodium et d’autres métaux de transition : s ynthèse verte d’oxazolidinones . [Internet] [Thesis]. Université de Montréal; 2016. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1866/13960.

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

Council of Science Editors:

Mamani Laparra L. Réaction d’amination intramoléculaire de liens C-H à partir de N-mésyloxycarbamates catalysée par des complexes de rhodium et d’autres métaux de transition : s ynthèse verte d’oxazolidinones . [Thesis]. Université de Montréal; 2016. Available from: http://hdl.handle.net/1866/13960

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

.