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You searched for subject:(Diastereoselective Synthesis of Planar Chiral Ferrocenes). Showing records 1 – 30 of 242578 total matches.

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Brock University

1. John, Joshni. Diastereoselective Synthesis of Planar Chiral N-Substituted Ferrocenes Derived from Epimeric Imidazolones and their Application to Asymmetric Hydrogenation of Quinolines .

Degree: Department of Chemistry, 2015, Brock University

 This thesis describes the synthesis and use of an N-substituted ferrocene bearing a proline-derived chiral directing group and diastereoselective lithiation-electrophile quench of the pro-Sp hydrogen… (more)

Subjects/Keywords: Diastereoselective Synthesis of Planar Chiral Ferrocenes; Asymmetric Hydrogenation of Quinolines

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

APA (6th Edition):

John, J. (2015). Diastereoselective Synthesis of Planar Chiral N-Substituted Ferrocenes Derived from Epimeric Imidazolones and their Application to Asymmetric Hydrogenation of Quinolines . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/6118

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):

John, Joshni. “Diastereoselective Synthesis of Planar Chiral N-Substituted Ferrocenes Derived from Epimeric Imidazolones and their Application to Asymmetric Hydrogenation of Quinolines .” 2015. Thesis, Brock University. Accessed October 20, 2019. http://hdl.handle.net/10464/6118.

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

MLA Handbook (7th Edition):

John, Joshni. “Diastereoselective Synthesis of Planar Chiral N-Substituted Ferrocenes Derived from Epimeric Imidazolones and their Application to Asymmetric Hydrogenation of Quinolines .” 2015. Web. 20 Oct 2019.

Vancouver:

John J. Diastereoselective Synthesis of Planar Chiral N-Substituted Ferrocenes Derived from Epimeric Imidazolones and their Application to Asymmetric Hydrogenation of Quinolines . [Internet] [Thesis]. Brock University; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10464/6118.

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

Council of Science Editors:

John J. Diastereoselective Synthesis of Planar Chiral N-Substituted Ferrocenes Derived from Epimeric Imidazolones and their Application to Asymmetric Hydrogenation of Quinolines . [Thesis]. Brock University; 2015. Available from: http://hdl.handle.net/10464/6118

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


Université Montpellier II

2. Geant, Pierre-Yves. Synthèse d'aminoalcools assistée par un sulfoxyde chiral : Synthesis of aminoalcohols assisted by a chiral sulfoxide.

Degree: Docteur es, Ingénérie Moléculaire, 2011, Université Montpellier II

Les travaux présentés dans ce mémoire décrivent une nouvelle voie de synthèse d'aminoalcools 1,2 à partir de γ-bromo-β-cétosulfoxydes, dans lesquels seul le centre stéréogène du… (more)

Subjects/Keywords: Synthèse asymétrique; Sulfoxyde chiral; Aminoalcool; Dédoublement cinétique dynamique; Réduction diastéréosélective; Alcaloïdes pipéridin-3-ol; Asymmetric synthesis; Chiral sulfoxide; Aminoalcohol; Dynamic kinetic resolution; Diastereoselective reduction; Piperidin-3-ol alkaloids

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APA (6th Edition):

Geant, P. (2011). Synthèse d'aminoalcools assistée par un sulfoxyde chiral : Synthesis of aminoalcohols assisted by a chiral sulfoxide. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2011MON20169

Chicago Manual of Style (16th Edition):

Geant, Pierre-Yves. “Synthèse d'aminoalcools assistée par un sulfoxyde chiral : Synthesis of aminoalcohols assisted by a chiral sulfoxide.” 2011. Doctoral Dissertation, Université Montpellier II. Accessed October 20, 2019. http://www.theses.fr/2011MON20169.

MLA Handbook (7th Edition):

Geant, Pierre-Yves. “Synthèse d'aminoalcools assistée par un sulfoxyde chiral : Synthesis of aminoalcohols assisted by a chiral sulfoxide.” 2011. Web. 20 Oct 2019.

Vancouver:

Geant P. Synthèse d'aminoalcools assistée par un sulfoxyde chiral : Synthesis of aminoalcohols assisted by a chiral sulfoxide. [Internet] [Doctoral dissertation]. Université Montpellier II; 2011. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2011MON20169.

Council of Science Editors:

Geant P. Synthèse d'aminoalcools assistée par un sulfoxyde chiral : Synthesis of aminoalcohols assisted by a chiral sulfoxide. [Doctoral Dissertation]. Université Montpellier II; 2011. Available from: http://www.theses.fr/2011MON20169


North Carolina State University

3. Capracotta, Sonja Siefert. Novel Chiral Diamines and (S)-6-Chloronicotine Derivatives as Catalysts for Asymmetric Synthesis.

Degree: PhD, Chemistry, 2009, North Carolina State University

 Many enantiomerically pure products with biological activities are commonly used in the pharmaceutical industry due to their effectiveness. As such, procedures that produce stereochemically pure… (more)

Subjects/Keywords: asymmetric synthesis; chiral amino alcohols; chiral catalyst; amino phosphines; nicotine; allylic alkylation; addition of diethylzinc to aldehydes; chiral diamines

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APA (6th Edition):

Capracotta, S. S. (2009). Novel Chiral Diamines and (S)-6-Chloronicotine Derivatives as Catalysts for Asymmetric Synthesis. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/4982

Chicago Manual of Style (16th Edition):

Capracotta, Sonja Siefert. “Novel Chiral Diamines and (S)-6-Chloronicotine Derivatives as Catalysts for Asymmetric Synthesis.” 2009. Doctoral Dissertation, North Carolina State University. Accessed October 20, 2019. http://www.lib.ncsu.edu/resolver/1840.16/4982.

MLA Handbook (7th Edition):

Capracotta, Sonja Siefert. “Novel Chiral Diamines and (S)-6-Chloronicotine Derivatives as Catalysts for Asymmetric Synthesis.” 2009. Web. 20 Oct 2019.

Vancouver:

Capracotta SS. Novel Chiral Diamines and (S)-6-Chloronicotine Derivatives as Catalysts for Asymmetric Synthesis. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2019 Oct 20]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4982.

Council of Science Editors:

Capracotta SS. Novel Chiral Diamines and (S)-6-Chloronicotine Derivatives as Catalysts for Asymmetric Synthesis. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4982


University of Bath

4. Zhang, Xiao-An. The diastereoselectivity of some novel organic reactions.

Degree: PhD, 1987, University of Bath

Subjects/Keywords: 547; Diastereoselective synthesis

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APA (6th Edition):

Zhang, X. (1987). The diastereoselectivity of some novel organic reactions. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/the-diastereoselectivity-of-some-novel-organic-reactions(8f5e0e6e-7634-4b49-961c-85e36a031538).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.377963

Chicago Manual of Style (16th Edition):

Zhang, Xiao-An. “The diastereoselectivity of some novel organic reactions.” 1987. Doctoral Dissertation, University of Bath. Accessed October 20, 2019. https://researchportal.bath.ac.uk/en/studentthesis/the-diastereoselectivity-of-some-novel-organic-reactions(8f5e0e6e-7634-4b49-961c-85e36a031538).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.377963.

MLA Handbook (7th Edition):

Zhang, Xiao-An. “The diastereoselectivity of some novel organic reactions.” 1987. Web. 20 Oct 2019.

Vancouver:

Zhang X. The diastereoselectivity of some novel organic reactions. [Internet] [Doctoral dissertation]. University of Bath; 1987. [cited 2019 Oct 20]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/the-diastereoselectivity-of-some-novel-organic-reactions(8f5e0e6e-7634-4b49-961c-85e36a031538).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.377963.

Council of Science Editors:

Zhang X. The diastereoselectivity of some novel organic reactions. [Doctoral Dissertation]. University of Bath; 1987. Available from: https://researchportal.bath.ac.uk/en/studentthesis/the-diastereoselectivity-of-some-novel-organic-reactions(8f5e0e6e-7634-4b49-961c-85e36a031538).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.377963


Université de Montréal

5. Jarvis, Scott. Enantiopure 3-substituted piperidines via an aziridinium ion ring expansion .

Degree: 2012, Université de Montréal

 Ce mémoire décrit le développement d’une nouvelle méthodologie d’expansion de cycle irréversible à partir de N-alkyl-3,4-déhydroprolinols pour former des N-alkyl tétrahydropyridines 3-substituées en passant par… (more)

Subjects/Keywords: Pipéridine; Piperidine; Tétrahydropyridine; Tetrahydropyridine; Aziridinium; Aziridinium; Synthèse énantiosélective; Enantioselective synthesis; Synthèse diastereoselective; Diastereoselective synthesis

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APA (6th Edition):

Jarvis, S. (2012). Enantiopure 3-substituted piperidines via an aziridinium ion ring expansion . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6878

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):

Jarvis, Scott. “Enantiopure 3-substituted piperidines via an aziridinium ion ring expansion .” 2012. Thesis, Université de Montréal. Accessed October 20, 2019. http://hdl.handle.net/1866/6878.

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

MLA Handbook (7th Edition):

Jarvis, Scott. “Enantiopure 3-substituted piperidines via an aziridinium ion ring expansion .” 2012. Web. 20 Oct 2019.

Vancouver:

Jarvis S. Enantiopure 3-substituted piperidines via an aziridinium ion ring expansion . [Internet] [Thesis]. Université de Montréal; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1866/6878.

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

Council of Science Editors:

Jarvis S. Enantiopure 3-substituted piperidines via an aziridinium ion ring expansion . [Thesis]. Université de Montréal; 2012. Available from: http://hdl.handle.net/1866/6878

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


University of Leicester

6. Selim, Mohammed Refat Moustafa. Studies on asymmetric induction.

Degree: PhD, 1987, University of Leicester

 As a part of our studies on asymmetric induction, four topics were investigated in this thesis. Firstly, optically active menthyl and neo-menthyl phos-phonoacetates were prepared… (more)

Subjects/Keywords: 547; Synthesis of chiral aldehyde

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APA (6th Edition):

Selim, M. R. M. (1987). Studies on asymmetric induction. (Doctoral Dissertation). University of Leicester. Retrieved from http://hdl.handle.net/2381/33892

Chicago Manual of Style (16th Edition):

Selim, Mohammed Refat Moustafa. “Studies on asymmetric induction.” 1987. Doctoral Dissertation, University of Leicester. Accessed October 20, 2019. http://hdl.handle.net/2381/33892.

MLA Handbook (7th Edition):

Selim, Mohammed Refat Moustafa. “Studies on asymmetric induction.” 1987. Web. 20 Oct 2019.

Vancouver:

Selim MRM. Studies on asymmetric induction. [Internet] [Doctoral dissertation]. University of Leicester; 1987. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2381/33892.

Council of Science Editors:

Selim MRM. Studies on asymmetric induction. [Doctoral Dissertation]. University of Leicester; 1987. Available from: http://hdl.handle.net/2381/33892


Vanderbilt University

7. Mathew, Priya Ann. Progress Towards the Total Synthesis of Mitomycin C.

Degree: PhD, Chemistry, 2012, Vanderbilt University

  Mitomycin C is a clinically used antitumor natural product isolated from <i>Streptomyces caespitosus</i>. The biological activity and synthetic challenge of mitomycin C has generated… (more)

Subjects/Keywords: diastereoselective synthesis of complex polycyclic aziridines; advanced intermediates to mitomycin C; convergent synthesis of mitomycin C; spiroketal formation; aminoquinone; halonium promoted alkynyl amine cyclization

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APA (6th Edition):

Mathew, P. A. (2012). Progress Towards the Total Synthesis of Mitomycin C. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-07202012-092011/ ;

Chicago Manual of Style (16th Edition):

Mathew, Priya Ann. “Progress Towards the Total Synthesis of Mitomycin C.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed October 20, 2019. http://etd.library.vanderbilt.edu//available/etd-07202012-092011/ ;.

MLA Handbook (7th Edition):

Mathew, Priya Ann. “Progress Towards the Total Synthesis of Mitomycin C.” 2012. Web. 20 Oct 2019.

Vancouver:

Mathew PA. Progress Towards the Total Synthesis of Mitomycin C. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2019 Oct 20]. Available from: http://etd.library.vanderbilt.edu//available/etd-07202012-092011/ ;.

Council of Science Editors:

Mathew PA. Progress Towards the Total Synthesis of Mitomycin C. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu//available/etd-07202012-092011/ ;


Vanderbilt University

8. Davis, Tyler Andrew. Electronic Modification and Development of a More Reactive Chiral Proton Catalyst for the Enantioselective Aza-Henry Reaction and its Application to the Synthesis of Therapeutics.

Degree: PhD, Chemistry, 2011, Vanderbilt University

 BisAMidine chiral proton catalysts are a class of mixed Brønsted acid/Brønsted base reagents amenable to both electronic and steric modification. A counterintuitive approach in which… (more)

Subjects/Keywords: Chiral Proton Catalysis; Aza-Henry Reaction; Enantioselective Synthesis of Nutlin-3; Chiral Bisamidine Catalyst; Asymmetric Catalysis; PBAM

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APA (6th Edition):

Davis, T. A. (2011). Electronic Modification and Development of a More Reactive Chiral Proton Catalyst for the Enantioselective Aza-Henry Reaction and its Application to the Synthesis of Therapeutics. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-07222011-142610/ ;

Chicago Manual of Style (16th Edition):

Davis, Tyler Andrew. “Electronic Modification and Development of a More Reactive Chiral Proton Catalyst for the Enantioselective Aza-Henry Reaction and its Application to the Synthesis of Therapeutics.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed October 20, 2019. http://etd.library.vanderbilt.edu//available/etd-07222011-142610/ ;.

MLA Handbook (7th Edition):

Davis, Tyler Andrew. “Electronic Modification and Development of a More Reactive Chiral Proton Catalyst for the Enantioselective Aza-Henry Reaction and its Application to the Synthesis of Therapeutics.” 2011. Web. 20 Oct 2019.

Vancouver:

Davis TA. Electronic Modification and Development of a More Reactive Chiral Proton Catalyst for the Enantioselective Aza-Henry Reaction and its Application to the Synthesis of Therapeutics. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Oct 20]. Available from: http://etd.library.vanderbilt.edu//available/etd-07222011-142610/ ;.

Council of Science Editors:

Davis TA. Electronic Modification and Development of a More Reactive Chiral Proton Catalyst for the Enantioselective Aza-Henry Reaction and its Application to the Synthesis of Therapeutics. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu//available/etd-07222011-142610/ ;

9. Dema, Haythem Karim. Chiral aldimines in diastereoselective carbon nucleophile additions.

Degree: 2018, Universidad de Alicante

Subjects/Keywords: Chiral aldimines; Diastereoselective additions; Indium; Allylations; Aza-Henry reaction; Malonic synthesis; Betalactams; Alpha-amino acids; Gamma-butyrolactams; Química Orgánica

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APA (6th Edition):

Dema, H. K. (2018). Chiral aldimines in diastereoselective carbon nucleophile additions. (Thesis). Universidad de Alicante. Retrieved from http://hdl.handle.net/10045/27136

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):

Dema, Haythem Karim. “Chiral aldimines in diastereoselective carbon nucleophile additions.” 2018. Thesis, Universidad de Alicante. Accessed October 20, 2019. http://hdl.handle.net/10045/27136.

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

MLA Handbook (7th Edition):

Dema, Haythem Karim. “Chiral aldimines in diastereoselective carbon nucleophile additions.” 2018. Web. 20 Oct 2019.

Vancouver:

Dema HK. Chiral aldimines in diastereoselective carbon nucleophile additions. [Internet] [Thesis]. Universidad de Alicante; 2018. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10045/27136.

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

Council of Science Editors:

Dema HK. Chiral aldimines in diastereoselective carbon nucleophile additions. [Thesis]. Universidad de Alicante; 2018. Available from: http://hdl.handle.net/10045/27136

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


University of Toronto

10. Dubland, Joshua. Studies towards Developing Diastereoselective SN1 Reactions of α-Keto Carbocations.

Degree: 2010, University of Toronto

Although α-keto carbocations have been demonstrated to be viable intermediates in solvolysis reactions, their applications in synthesis are scarce. These species can be considered to… (more)

Subjects/Keywords: diastereoselective SN1 reaction; alpha-keto carbocation; nucleophilic substitution reaction; carbon-carbon bond forming reaction; carbon-heteroatom bond forming reaction; chiral auxiliary; asymmetric synthesis; Lewis acid-mediated; Bronsted acid-mediated; silver-mediated; organic chemistry; leaving group; ester; amide; imide; 0490; 0485

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APA (6th Edition):

Dubland, J. (2010). Studies towards Developing Diastereoselective SN1 Reactions of α-Keto Carbocations. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/24246

Chicago Manual of Style (16th Edition):

Dubland, Joshua. “Studies towards Developing Diastereoselective SN1 Reactions of α-Keto Carbocations.” 2010. Masters Thesis, University of Toronto. Accessed October 20, 2019. http://hdl.handle.net/1807/24246.

MLA Handbook (7th Edition):

Dubland, Joshua. “Studies towards Developing Diastereoselective SN1 Reactions of α-Keto Carbocations.” 2010. Web. 20 Oct 2019.

Vancouver:

Dubland J. Studies towards Developing Diastereoselective SN1 Reactions of α-Keto Carbocations. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1807/24246.

Council of Science Editors:

Dubland J. Studies towards Developing Diastereoselective SN1 Reactions of α-Keto Carbocations. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24246


University of Manchester

11. Aldosari, Obaid Fahad. Synthesis of Some Novel Chiral Dendrimers 1,1-Binaphthyl Derivatives.

Degree: 2011, University of Manchester

Despite a number of reports on synthetic methods for 1,1'- binaphthyl molecules with a substitution in certain positions, to the best of our knowledge neither… (more)

Subjects/Keywords: Synthesis; Chiral; Bionapthol; Core; Dendrimers

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APA (6th Edition):

Aldosari, O. F. (2011). Synthesis of Some Novel Chiral Dendrimers 1,1-Binaphthyl Derivatives. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:110962

Chicago Manual of Style (16th Edition):

Aldosari, Obaid Fahad. “Synthesis of Some Novel Chiral Dendrimers 1,1-Binaphthyl Derivatives.” 2011. Doctoral Dissertation, University of Manchester. Accessed October 20, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:110962.

MLA Handbook (7th Edition):

Aldosari, Obaid Fahad. “Synthesis of Some Novel Chiral Dendrimers 1,1-Binaphthyl Derivatives.” 2011. Web. 20 Oct 2019.

Vancouver:

Aldosari OF. Synthesis of Some Novel Chiral Dendrimers 1,1-Binaphthyl Derivatives. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2019 Oct 20]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:110962.

Council of Science Editors:

Aldosari OF. Synthesis of Some Novel Chiral Dendrimers 1,1-Binaphthyl Derivatives. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:110962


Brock University

12. Sadraei, Seyed Iraj. Diastereoselective Lithiation-Substitution of N-Silyl-Protected-(S)-Tetrahydro-1H-pyrrolo[1,2-c]imidazole-3(2H)-ones and Applications of Their Derivatives .

Degree: Department of Chemistry, 2014, Brock University

 This thesis describes a method involving the preparation of an L-proline-derived imidazolone protected with an N-triethylsilyl group that undergoes diastereoselective lithiation followed by electrophile quench… (more)

Subjects/Keywords: L-proline-derived; imidazolone protected; diastereoselective lithiation; chiral guanidines; N-heterocyclic carbene complexes

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APA (6th Edition):

Sadraei, S. I. (2014). Diastereoselective Lithiation-Substitution of N-Silyl-Protected-(S)-Tetrahydro-1H-pyrrolo[1,2-c]imidazole-3(2H)-ones and Applications of Their Derivatives . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/5696

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):

Sadraei, Seyed Iraj. “Diastereoselective Lithiation-Substitution of N-Silyl-Protected-(S)-Tetrahydro-1H-pyrrolo[1,2-c]imidazole-3(2H)-ones and Applications of Their Derivatives .” 2014. Thesis, Brock University. Accessed October 20, 2019. http://hdl.handle.net/10464/5696.

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

MLA Handbook (7th Edition):

Sadraei, Seyed Iraj. “Diastereoselective Lithiation-Substitution of N-Silyl-Protected-(S)-Tetrahydro-1H-pyrrolo[1,2-c]imidazole-3(2H)-ones and Applications of Their Derivatives .” 2014. Web. 20 Oct 2019.

Vancouver:

Sadraei SI. Diastereoselective Lithiation-Substitution of N-Silyl-Protected-(S)-Tetrahydro-1H-pyrrolo[1,2-c]imidazole-3(2H)-ones and Applications of Their Derivatives . [Internet] [Thesis]. Brock University; 2014. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10464/5696.

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

Council of Science Editors:

Sadraei SI. Diastereoselective Lithiation-Substitution of N-Silyl-Protected-(S)-Tetrahydro-1H-pyrrolo[1,2-c]imidazole-3(2H)-ones and Applications of Their Derivatives . [Thesis]. Brock University; 2014. Available from: http://hdl.handle.net/10464/5696

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

13. Gratais, Alexandre. Chimie des acrylamides chiraux : nouvelles méthodologies et application à la synthèse de nouvelles architectures moléculaires : Chemistry of chiral acrylamides : new methodologies and application to the synthesisof new molecular architectures.

Degree: Docteur es, Chimie organique, 2014, Rouen, INSA

Les réactions permettant la création de liaisons carbone-carbone sont des outils essentiels dans le domaine de la synthèse organique. Elles permettent d'accéder à des structures… (more)

Subjects/Keywords: Allylsilanes chiraux; Allylation diastéréosélective; Chiral acrylamides; Peptides; Pyrrole; Friedel-Crafts alkylation; Chiral allylsilanes; Diastereoselective allylation; 547

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APA (6th Edition):

Gratais, A. (2014). Chimie des acrylamides chiraux : nouvelles méthodologies et application à la synthèse de nouvelles architectures moléculaires : Chemistry of chiral acrylamides : new methodologies and application to the synthesisof new molecular architectures. (Doctoral Dissertation). Rouen, INSA. Retrieved from http://www.theses.fr/2014ISAM0013

Chicago Manual of Style (16th Edition):

Gratais, Alexandre. “Chimie des acrylamides chiraux : nouvelles méthodologies et application à la synthèse de nouvelles architectures moléculaires : Chemistry of chiral acrylamides : new methodologies and application to the synthesisof new molecular architectures.” 2014. Doctoral Dissertation, Rouen, INSA. Accessed October 20, 2019. http://www.theses.fr/2014ISAM0013.

MLA Handbook (7th Edition):

Gratais, Alexandre. “Chimie des acrylamides chiraux : nouvelles méthodologies et application à la synthèse de nouvelles architectures moléculaires : Chemistry of chiral acrylamides : new methodologies and application to the synthesisof new molecular architectures.” 2014. Web. 20 Oct 2019.

Vancouver:

Gratais A. Chimie des acrylamides chiraux : nouvelles méthodologies et application à la synthèse de nouvelles architectures moléculaires : Chemistry of chiral acrylamides : new methodologies and application to the synthesisof new molecular architectures. [Internet] [Doctoral dissertation]. Rouen, INSA; 2014. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2014ISAM0013.

Council of Science Editors:

Gratais A. Chimie des acrylamides chiraux : nouvelles méthodologies et application à la synthèse de nouvelles architectures moléculaires : Chemistry of chiral acrylamides : new methodologies and application to the synthesisof new molecular architectures. [Doctoral Dissertation]. Rouen, INSA; 2014. Available from: http://www.theses.fr/2014ISAM0013


Case Western Reserve University

14. KANISKAN, H. ÜMIT. A FORMAL TOTAL SYNTHESIS OF BIOXALOMYCIN BETA 2.

Degree: PhD, Chemistry, 2007, Case Western Reserve University

 A new cycloadditive approach for the asymmetric synthesis of the bioxalomycin family of antitumor antibiotics has been developed. Through this new synthetic route, a formal… (more)

Subjects/Keywords: Chemistry, Organic; total synthesis of bioxalomycin; pyrrolidines; 1,3-dipolar cycloaddition; chiral azomethine ylides

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APA (6th Edition):

KANISKAN, H. . (2007). A FORMAL TOTAL SYNTHESIS OF BIOXALOMYCIN BETA 2. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1180451443

Chicago Manual of Style (16th Edition):

KANISKAN, H ÜMIT. “A FORMAL TOTAL SYNTHESIS OF BIOXALOMYCIN BETA 2.” 2007. Doctoral Dissertation, Case Western Reserve University. Accessed October 20, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1180451443.

MLA Handbook (7th Edition):

KANISKAN, H ÜMIT. “A FORMAL TOTAL SYNTHESIS OF BIOXALOMYCIN BETA 2.” 2007. Web. 20 Oct 2019.

Vancouver:

KANISKAN H. A FORMAL TOTAL SYNTHESIS OF BIOXALOMYCIN BETA 2. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2007. [cited 2019 Oct 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1180451443.

Council of Science Editors:

KANISKAN H. A FORMAL TOTAL SYNTHESIS OF BIOXALOMYCIN BETA 2. [Doctoral Dissertation]. Case Western Reserve University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1180451443


Curtin University of Technology

15. McIldowie, Matthew. The synthesis and structure of C4 symmetric resorcinarenes .

Degree: 2007, Curtin University of Technology

 This study investigates methods for the synthesis and resolution of chiral resorcinarenes.The first direct synthesis of C4 dissymmetric resorcinarenes by the Lewis acid catalysed condensation… (more)

Subjects/Keywords: synthesis and resolution of chiral resorcinarenes

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APA (6th Edition):

McIldowie, M. (2007). The synthesis and structure of C4 symmetric resorcinarenes . (Thesis). Curtin University of Technology. Retrieved from http://hdl.handle.net/20.500.11937/1565

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):

McIldowie, Matthew. “The synthesis and structure of C4 symmetric resorcinarenes .” 2007. Thesis, Curtin University of Technology. Accessed October 20, 2019. http://hdl.handle.net/20.500.11937/1565.

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

MLA Handbook (7th Edition):

McIldowie, Matthew. “The synthesis and structure of C4 symmetric resorcinarenes .” 2007. Web. 20 Oct 2019.

Vancouver:

McIldowie M. The synthesis and structure of C4 symmetric resorcinarenes . [Internet] [Thesis]. Curtin University of Technology; 2007. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/20.500.11937/1565.

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

Council of Science Editors:

McIldowie M. The synthesis and structure of C4 symmetric resorcinarenes . [Thesis]. Curtin University of Technology; 2007. Available from: http://hdl.handle.net/20.500.11937/1565

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


University of Wisconsin – Milwaukee

16. Uddin, Md Nazim. I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B.

Degree: PhD, Chemistry, 2015, University of Wisconsin – Milwaukee

  The development of efficient catalytic enantioselective synthesis of all carbon quaternary centers is a significant challenge in chemical synthesis due to the difficulties of… (more)

Subjects/Keywords: Asymmetric Allylic Alkylation; Asymmetric Synthesis; Organometallic Chemistry; Phase Transfer Catalysis; Synthesis of Chiral Tryptophans and Total Synthesis of Tryprostatin; Synthesis of Quaternary Stereocenter; Chemistry; Organic Chemistry

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APA (6th Edition):

Uddin, M. N. (2015). I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B. (Doctoral Dissertation). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/931

Chicago Manual of Style (16th Edition):

Uddin, Md Nazim. “I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B.” 2015. Doctoral Dissertation, University of Wisconsin – Milwaukee. Accessed October 20, 2019. https://dc.uwm.edu/etd/931.

MLA Handbook (7th Edition):

Uddin, Md Nazim. “I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B.” 2015. Web. 20 Oct 2019.

Vancouver:

Uddin MN. I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B. [Internet] [Doctoral dissertation]. University of Wisconsin – Milwaukee; 2015. [cited 2019 Oct 20]. Available from: https://dc.uwm.edu/etd/931.

Council of Science Editors:

Uddin MN. I. Palladium (0)-Catalyzed Asymmetric Rearrangement of Allyl Enol Ether for the Synthesis of Α -aryl Quaternary Carbon Center. II. Synthesis of Chiral Tryptophan Analogs and Studies Towards Synthesis of Tryprostatin A and B. [Doctoral Dissertation]. University of Wisconsin – Milwaukee; 2015. Available from: https://dc.uwm.edu/etd/931


Université Paris-Sud – Paris XI

17. Abada, Zahra. Synthèse de porphyrines chirales : application en oxydation asymétrique et application antiparasitaire et anticancéreuse : Synthesis of chiral porphyrins : Application in asymmetric oxidation and applications as anticancerous and antiparasitic agents.

Degree: Docteur es, Synthèse organique, 2012, Université Paris-Sud – Paris XI

 Les molécules chirales représentent environ 60% des médicaments présents sur le marché pharmaceutique et plus de 80% des médicaments en développement avec plus de 150… (more)

Subjects/Keywords: Thérapie photodynamique; Synthèse asymétrique; Cible antiparasitaire; Cible anticancéreuse; Synthesis of chiral porphyrins; Olefin enantioselective oxidation; Chiral catalysis; Asymmetric synthesis; Antiparasitic therapy; Cancer therapy; Photodynamic therapy

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APA (6th Edition):

Abada, Z. (2012). Synthèse de porphyrines chirales : application en oxydation asymétrique et application antiparasitaire et anticancéreuse : Synthesis of chiral porphyrins : Application in asymmetric oxidation and applications as anticancerous and antiparasitic agents. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA114806

Chicago Manual of Style (16th Edition):

Abada, Zahra. “Synthèse de porphyrines chirales : application en oxydation asymétrique et application antiparasitaire et anticancéreuse : Synthesis of chiral porphyrins : Application in asymmetric oxidation and applications as anticancerous and antiparasitic agents.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 20, 2019. http://www.theses.fr/2012PA114806.

MLA Handbook (7th Edition):

Abada, Zahra. “Synthèse de porphyrines chirales : application en oxydation asymétrique et application antiparasitaire et anticancéreuse : Synthesis of chiral porphyrins : Application in asymmetric oxidation and applications as anticancerous and antiparasitic agents.” 2012. Web. 20 Oct 2019.

Vancouver:

Abada Z. Synthèse de porphyrines chirales : application en oxydation asymétrique et application antiparasitaire et anticancéreuse : Synthesis of chiral porphyrins : Application in asymmetric oxidation and applications as anticancerous and antiparasitic agents. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2012PA114806.

Council of Science Editors:

Abada Z. Synthèse de porphyrines chirales : application en oxydation asymétrique et application antiparasitaire et anticancéreuse : Synthesis of chiral porphyrins : Application in asymmetric oxidation and applications as anticancerous and antiparasitic agents. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA114806


University of California – Irvine

18. Uchenik, Dmitriy. Studies of Halogenated Lipids and Progress Toward the Synthesis of Crotogoudin.

Degree: Chemistry, 2017, University of California – Irvine

 ABSTRACT OF THE DISSERTATIONStudies of Halogenated Lipids andProgress Toward the Synthesis of CrotogoudinByDmitriy Igorovich UchenikDoctor of Philosophy in ChemistryUniversity of California, Irvine, 2017Professor Christopher D.… (more)

Subjects/Keywords: Chemistry; Conjugate Reduction; Diastereoselective Eliminations; Free Radical Cyclization; Natural Product Synthesis

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APA (6th Edition):

Uchenik, D. (2017). Studies of Halogenated Lipids and Progress Toward the Synthesis of Crotogoudin. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/2hc28159

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):

Uchenik, Dmitriy. “Studies of Halogenated Lipids and Progress Toward the Synthesis of Crotogoudin.” 2017. Thesis, University of California – Irvine. Accessed October 20, 2019. http://www.escholarship.org/uc/item/2hc28159.

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

MLA Handbook (7th Edition):

Uchenik, Dmitriy. “Studies of Halogenated Lipids and Progress Toward the Synthesis of Crotogoudin.” 2017. Web. 20 Oct 2019.

Vancouver:

Uchenik D. Studies of Halogenated Lipids and Progress Toward the Synthesis of Crotogoudin. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2019 Oct 20]. Available from: http://www.escholarship.org/uc/item/2hc28159.

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

Council of Science Editors:

Uchenik D. Studies of Halogenated Lipids and Progress Toward the Synthesis of Crotogoudin. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/2hc28159

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

19. Zarate Ruiz, Griselda Araceli. Vers la synthèse totale de la Thuggacine A : Approach to the total synthesis of Thuggacin A.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2011, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier)

Le travail présenté dans ce manuscrit concerne la synthèse du fragment C12-C25 de la Thuggacine A, macrolide antibiotique, par deux voies de synthèse. La première… (more)

Subjects/Keywords: Antituberculeux; Aldolisation; Macrolide; Synthèse diastéréosélective; Antituberculotic; Aldolization; Macrolide; Diastereoselective synthesis

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APA (6th Edition):

Zarate Ruiz, G. A. (2011). Vers la synthèse totale de la Thuggacine A : Approach to the total synthesis of Thuggacin A. (Doctoral Dissertation). Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Retrieved from http://www.theses.fr/2011ENCM0002

Chicago Manual of Style (16th Edition):

Zarate Ruiz, Griselda Araceli. “Vers la synthèse totale de la Thuggacine A : Approach to the total synthesis of Thuggacin A.” 2011. Doctoral Dissertation, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Accessed October 20, 2019. http://www.theses.fr/2011ENCM0002.

MLA Handbook (7th Edition):

Zarate Ruiz, Griselda Araceli. “Vers la synthèse totale de la Thuggacine A : Approach to the total synthesis of Thuggacin A.” 2011. Web. 20 Oct 2019.

Vancouver:

Zarate Ruiz GA. Vers la synthèse totale de la Thuggacine A : Approach to the total synthesis of Thuggacin A. [Internet] [Doctoral dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2011. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2011ENCM0002.

Council of Science Editors:

Zarate Ruiz GA. Vers la synthèse totale de la Thuggacine A : Approach to the total synthesis of Thuggacin A. [Doctoral Dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2011. Available from: http://www.theses.fr/2011ENCM0002


California State University – Sacramento

20. Kavikondala, Pawan. Generalized analytic method for near-field reconstruction of antenna currents in microwave hyperthermia cancer treatment systems.

Degree: MS, Electrical and Electronic Engineering, 2010, California State University – Sacramento

 Currently chemotherapy radiation and surgery are the standard treatments for cancer that are widely accepted and used. However, a fourth modality is emerging as an… (more)

Subjects/Keywords: Synthesis of planar, cylindrical and circular arrays; Identification of defective antenna; Matlab programs for different arrays

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APA (6th Edition):

Kavikondala, P. (2010). Generalized analytic method for near-field reconstruction of antenna currents in microwave hyperthermia cancer treatment systems. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.9/357

Chicago Manual of Style (16th Edition):

Kavikondala, Pawan. “Generalized analytic method for near-field reconstruction of antenna currents in microwave hyperthermia cancer treatment systems.” 2010. Masters Thesis, California State University – Sacramento. Accessed October 20, 2019. http://hdl.handle.net/10211.9/357.

MLA Handbook (7th Edition):

Kavikondala, Pawan. “Generalized analytic method for near-field reconstruction of antenna currents in microwave hyperthermia cancer treatment systems.” 2010. Web. 20 Oct 2019.

Vancouver:

Kavikondala P. Generalized analytic method for near-field reconstruction of antenna currents in microwave hyperthermia cancer treatment systems. [Internet] [Masters thesis]. California State University – Sacramento; 2010. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10211.9/357.

Council of Science Editors:

Kavikondala P. Generalized analytic method for near-field reconstruction of antenna currents in microwave hyperthermia cancer treatment systems. [Masters Thesis]. California State University – Sacramento; 2010. Available from: http://hdl.handle.net/10211.9/357


University of Toronto

21. Golas, Ewa. Stereoselective and Stereospecific Interactions with Amino Acids.

Degree: 2010, University of Toronto

The following study investigates the intramolecular and intermolecular interactions responsible for invoking stereoselectivity and stereospecificity in the synthesis of a chiral original species and amino… (more)

Subjects/Keywords: receptor; enantiomer; amino acid; sensor; lactone; helical; imine; chiral; helix; computation; computational; stereoselectivity; diastereoselective; stereospecific; 0490

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APA (6th Edition):

Golas, E. (2010). Stereoselective and Stereospecific Interactions with Amino Acids. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25598

Chicago Manual of Style (16th Edition):

Golas, Ewa. “Stereoselective and Stereospecific Interactions with Amino Acids.” 2010. Masters Thesis, University of Toronto. Accessed October 20, 2019. http://hdl.handle.net/1807/25598.

MLA Handbook (7th Edition):

Golas, Ewa. “Stereoselective and Stereospecific Interactions with Amino Acids.” 2010. Web. 20 Oct 2019.

Vancouver:

Golas E. Stereoselective and Stereospecific Interactions with Amino Acids. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1807/25598.

Council of Science Editors:

Golas E. Stereoselective and Stereospecific Interactions with Amino Acids. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25598


Kansas State University

22. Almkhelfe, Haider H. Scalable carbon nanotube growth and design of efficient catalysts for Fischer-Tropsch synthesis.

Degree: PhD, Department of Chemical Engineering, 2017, Kansas State University

 The continued depletion of fossil fuels and concomitant increase in greenhouse gases have encouraged worldwide research on alternative processes to produce clean fuel. Fischer-Tropsch synthesis(more)

Subjects/Keywords: Fischer-Tropsch synthesis; Synthesis carbon nanomaterials; Chiral and diameter control of single wall carbon nanotubes (SWCNTs); Carbon nanotubes (CNTs); Gaseous product mixture from Fischer-Tropsch synthesis (FTS-GP)

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APA (6th Edition):

Almkhelfe, H. H. (2017). Scalable carbon nanotube growth and design of efficient catalysts for Fischer-Tropsch synthesis. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/38213

Chicago Manual of Style (16th Edition):

Almkhelfe, Haider H. “Scalable carbon nanotube growth and design of efficient catalysts for Fischer-Tropsch synthesis.” 2017. Doctoral Dissertation, Kansas State University. Accessed October 20, 2019. http://hdl.handle.net/2097/38213.

MLA Handbook (7th Edition):

Almkhelfe, Haider H. “Scalable carbon nanotube growth and design of efficient catalysts for Fischer-Tropsch synthesis.” 2017. Web. 20 Oct 2019.

Vancouver:

Almkhelfe HH. Scalable carbon nanotube growth and design of efficient catalysts for Fischer-Tropsch synthesis. [Internet] [Doctoral dissertation]. Kansas State University; 2017. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2097/38213.

Council of Science Editors:

Almkhelfe HH. Scalable carbon nanotube growth and design of efficient catalysts for Fischer-Tropsch synthesis. [Doctoral Dissertation]. Kansas State University; 2017. Available from: http://hdl.handle.net/2097/38213

23. Prasanta Kumar, Bera. Synthesis, Characterization and Evaluation of Chiral Catalysts for Commercially Important Asymmetric Oxidative Organic Transformations;.

Degree: Chemistry, 2014, Maharaja Krishnakumarsinhji Bhavnagar University

None newline

Reference given in chapters.

Advisors/Committee Members: Sayed Hasan Razi Abdi.

Subjects/Keywords: Characterization; Evaluation of Chiral Catalysts; Oxidative Organic Transformations; Synthesis

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APA (6th Edition):

Prasanta Kumar, B. (2014). Synthesis, Characterization and Evaluation of Chiral Catalysts for Commercially Important Asymmetric Oxidative Organic Transformations;. (Thesis). Maharaja Krishnakumarsinhji Bhavnagar University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/35843

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):

Prasanta Kumar, Bera. “Synthesis, Characterization and Evaluation of Chiral Catalysts for Commercially Important Asymmetric Oxidative Organic Transformations;.” 2014. Thesis, Maharaja Krishnakumarsinhji Bhavnagar University. Accessed October 20, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/35843.

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

MLA Handbook (7th Edition):

Prasanta Kumar, Bera. “Synthesis, Characterization and Evaluation of Chiral Catalysts for Commercially Important Asymmetric Oxidative Organic Transformations;.” 2014. Web. 20 Oct 2019.

Vancouver:

Prasanta Kumar B. Synthesis, Characterization and Evaluation of Chiral Catalysts for Commercially Important Asymmetric Oxidative Organic Transformations;. [Internet] [Thesis]. Maharaja Krishnakumarsinhji Bhavnagar University; 2014. [cited 2019 Oct 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/35843.

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

Council of Science Editors:

Prasanta Kumar B. Synthesis, Characterization and Evaluation of Chiral Catalysts for Commercially Important Asymmetric Oxidative Organic Transformations;. [Thesis]. Maharaja Krishnakumarsinhji Bhavnagar University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/35843

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


Brock University

24. Whitbread, Kristina Marie. Synthesis of chiral homoallylic alcohols and phthalans through the asymmetric allylation of carbonyl compounds .

Degree: Department of Biological Sciences, 2009, Brock University

 The implementation of chiral centres within biologically active compounds has been a perplexing yet motivational force in chemistry. This work presents the attempted formation of… (more)

Subjects/Keywords: Asymmetric synthesis.; Carbonyl compounds.; Chiral drugs.; Biochemistry.

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APA (6th Edition):

Whitbread, K. M. (2009). Synthesis of chiral homoallylic alcohols and phthalans through the asymmetric allylation of carbonyl compounds . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/1603

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):

Whitbread, Kristina Marie. “Synthesis of chiral homoallylic alcohols and phthalans through the asymmetric allylation of carbonyl compounds .” 2009. Thesis, Brock University. Accessed October 20, 2019. http://hdl.handle.net/10464/1603.

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

MLA Handbook (7th Edition):

Whitbread, Kristina Marie. “Synthesis of chiral homoallylic alcohols and phthalans through the asymmetric allylation of carbonyl compounds .” 2009. Web. 20 Oct 2019.

Vancouver:

Whitbread KM. Synthesis of chiral homoallylic alcohols and phthalans through the asymmetric allylation of carbonyl compounds . [Internet] [Thesis]. Brock University; 2009. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10464/1603.

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

Council of Science Editors:

Whitbread KM. Synthesis of chiral homoallylic alcohols and phthalans through the asymmetric allylation of carbonyl compounds . [Thesis]. Brock University; 2009. Available from: http://hdl.handle.net/10464/1603

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


Virginia Tech

25. Khan, Iqtidar Ahmad. Analysis and Synthesis of a New Class of Low Side Lobe Planar Arrays.

Degree: MS, Electrical Engineering, 2018, Virginia Tech

 Numerical techniques for designing planar arrays with low side lobe level often require memory intensive optimization algorithms and also initialization in the form of some… (more)

Subjects/Keywords: planar arrays; array synthesis; rectangular arrays; low side lobe planar arrays.

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APA (6th Edition):

Khan, I. A. (2018). Analysis and Synthesis of a New Class of Low Side Lobe Planar Arrays. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/93222

Chicago Manual of Style (16th Edition):

Khan, Iqtidar Ahmad. “Analysis and Synthesis of a New Class of Low Side Lobe Planar Arrays.” 2018. Masters Thesis, Virginia Tech. Accessed October 20, 2019. http://hdl.handle.net/10919/93222.

MLA Handbook (7th Edition):

Khan, Iqtidar Ahmad. “Analysis and Synthesis of a New Class of Low Side Lobe Planar Arrays.” 2018. Web. 20 Oct 2019.

Vancouver:

Khan IA. Analysis and Synthesis of a New Class of Low Side Lobe Planar Arrays. [Internet] [Masters thesis]. Virginia Tech; 2018. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10919/93222.

Council of Science Editors:

Khan IA. Analysis and Synthesis of a New Class of Low Side Lobe Planar Arrays. [Masters Thesis]. Virginia Tech; 2018. Available from: http://hdl.handle.net/10919/93222


Vanderbilt University

26. Muchalski, Hubert. Stereospecific Reactions of α-Amino-β-Diazonium Intermediates: Mechanistic Studies, New Reaction Discovery and their Application to a Two-Directional Total Synthesis Of (+)-Zwittermicin A.

Degree: PhD, Chemistry, 2012, Vanderbilt University

  This dissertation is concerned with the stereospecific transformations of α-amino-β-diazonium intermediates. The mechanism of the Brønsted acid-catalyzed aza-Darzens reaction is explored by charting the… (more)

Subjects/Keywords: two-directional synthesis; total synthesis; bidirectional synthesis; cycloaddition; aminoalcohols; diazoimide; diastereoselective reaction; TIPDS; zwittermicin A; Huisgen; diazo compounds; aza-Darzens reaction

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APA (6th Edition):

Muchalski, H. (2012). Stereospecific Reactions of α-Amino-β-Diazonium Intermediates: Mechanistic Studies, New Reaction Discovery and their Application to a Two-Directional Total Synthesis Of (+)-Zwittermicin A. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-07102012-175202/ ;

Chicago Manual of Style (16th Edition):

Muchalski, Hubert. “Stereospecific Reactions of α-Amino-β-Diazonium Intermediates: Mechanistic Studies, New Reaction Discovery and their Application to a Two-Directional Total Synthesis Of (+)-Zwittermicin A.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed October 20, 2019. http://etd.library.vanderbilt.edu//available/etd-07102012-175202/ ;.

MLA Handbook (7th Edition):

Muchalski, Hubert. “Stereospecific Reactions of α-Amino-β-Diazonium Intermediates: Mechanistic Studies, New Reaction Discovery and their Application to a Two-Directional Total Synthesis Of (+)-Zwittermicin A.” 2012. Web. 20 Oct 2019.

Vancouver:

Muchalski H. Stereospecific Reactions of α-Amino-β-Diazonium Intermediates: Mechanistic Studies, New Reaction Discovery and their Application to a Two-Directional Total Synthesis Of (+)-Zwittermicin A. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2019 Oct 20]. Available from: http://etd.library.vanderbilt.edu//available/etd-07102012-175202/ ;.

Council of Science Editors:

Muchalski H. Stereospecific Reactions of α-Amino-β-Diazonium Intermediates: Mechanistic Studies, New Reaction Discovery and their Application to a Two-Directional Total Synthesis Of (+)-Zwittermicin A. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu//available/etd-07102012-175202/ ;


Baylor University

27. Van der Velde, Nelson A. Synthesis of new chiral pyrylium salts, the corresponding phosphinine and pyridine derivatives and the kinetic studies of the epimerization of pyrylium salts.

Degree: Chemistry and Biochemistry., 2013, Baylor University

 Despite the versatility of pyrylium salts as precursors to many heteroaromatic systems, chiral pyrylium salts are almost unknown in the literature. One reason for this… (more)

Subjects/Keywords: Chiral pyrylium salts.; Chiral phosphinines.; Chiral pyridines.; Epimerization of chiral pyrylium salts.

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APA (6th Edition):

Van der Velde, N. A. (2013). Synthesis of new chiral pyrylium salts, the corresponding phosphinine and pyridine derivatives and the kinetic studies of the epimerization of pyrylium salts. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/8732

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 der Velde, Nelson A. “Synthesis of new chiral pyrylium salts, the corresponding phosphinine and pyridine derivatives and the kinetic studies of the epimerization of pyrylium salts. ” 2013. Thesis, Baylor University. Accessed October 20, 2019. http://hdl.handle.net/2104/8732.

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

MLA Handbook (7th Edition):

Van der Velde, Nelson A. “Synthesis of new chiral pyrylium salts, the corresponding phosphinine and pyridine derivatives and the kinetic studies of the epimerization of pyrylium salts. ” 2013. Web. 20 Oct 2019.

Vancouver:

Van der Velde NA. Synthesis of new chiral pyrylium salts, the corresponding phosphinine and pyridine derivatives and the kinetic studies of the epimerization of pyrylium salts. [Internet] [Thesis]. Baylor University; 2013. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2104/8732.

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

Council of Science Editors:

Van der Velde NA. Synthesis of new chiral pyrylium salts, the corresponding phosphinine and pyridine derivatives and the kinetic studies of the epimerization of pyrylium salts. [Thesis]. Baylor University; 2013. Available from: http://hdl.handle.net/2104/8732

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


Université Paris-Sud – Paris XI

28. Mai, Thi thoa. Nouvelles voies d’accès à des acides alpha-aminés énantioenrichis par mémoire de chiralité ou chiralité gelée : Memory of chirality or frozen chirality of tertiary aromatique amides : access to enantioenriched alpha-amino acids.

Degree: Docteur es, Chimie organique, 2012, Université Paris-Sud – Paris XI

Les acides α-aminés non protéinogènes sont des composés riches d’applications et peuvent donner accès à des composés possédant des propriétés biologiques intéressantes ou à des… (more)

Subjects/Keywords: Mémoire de chiralité; Amide aromatique; Acide α-aminé; Chiralité axiale; Alkylation de l’énolate; Synthèse asymétrique absolue; Chiralité gelée; Cristal chiral; Cristallisation chirale; Memory of chirality; Aromatic amide; Amino acid; Axial chirality; Alkylation of an enolate; Asymmetric absolute synthesis; Frozen chirality; Chiral crystal; Chiral crystallisation

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APA (6th Edition):

Mai, T. t. (2012). Nouvelles voies d’accès à des acides alpha-aminés énantioenrichis par mémoire de chiralité ou chiralité gelée : Memory of chirality or frozen chirality of tertiary aromatique amides : access to enantioenriched alpha-amino acids. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA112045

Chicago Manual of Style (16th Edition):

Mai, Thi thoa. “Nouvelles voies d’accès à des acides alpha-aminés énantioenrichis par mémoire de chiralité ou chiralité gelée : Memory of chirality or frozen chirality of tertiary aromatique amides : access to enantioenriched alpha-amino acids.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 20, 2019. http://www.theses.fr/2012PA112045.

MLA Handbook (7th Edition):

Mai, Thi thoa. “Nouvelles voies d’accès à des acides alpha-aminés énantioenrichis par mémoire de chiralité ou chiralité gelée : Memory of chirality or frozen chirality of tertiary aromatique amides : access to enantioenriched alpha-amino acids.” 2012. Web. 20 Oct 2019.

Vancouver:

Mai Tt. Nouvelles voies d’accès à des acides alpha-aminés énantioenrichis par mémoire de chiralité ou chiralité gelée : Memory of chirality or frozen chirality of tertiary aromatique amides : access to enantioenriched alpha-amino acids. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2012PA112045.

Council of Science Editors:

Mai Tt. Nouvelles voies d’accès à des acides alpha-aminés énantioenrichis par mémoire de chiralité ou chiralité gelée : Memory of chirality or frozen chirality of tertiary aromatique amides : access to enantioenriched alpha-amino acids. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA112045


Stellenbosch University

29. Kleinhans, Dewald Johannes. Studies in the synthesis of benzoxazole compounds.

Degree: PhD, Chemistry and Polymer Science, 2015, Stellenbosch University

ENGLISH ABSTRACT: Benzoxazoles are an important class of π-electron-excessive, benzene-fused heterocyclic compounds found in natural products and display a wide range of pharmacological applications. It… (more)

Subjects/Keywords: Benzoxazole  – Synthesis; Coordination compounds; Chiral ligands; Organic synthesis; Heterocyclic compounds; UCTD

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

APA (6th Edition):

Kleinhans, D. J. (2015). Studies in the synthesis of benzoxazole compounds. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/97900

Chicago Manual of Style (16th Edition):

Kleinhans, Dewald Johannes. “Studies in the synthesis of benzoxazole compounds.” 2015. Doctoral Dissertation, Stellenbosch University. Accessed October 20, 2019. http://hdl.handle.net/10019.1/97900.

MLA Handbook (7th Edition):

Kleinhans, Dewald Johannes. “Studies in the synthesis of benzoxazole compounds.” 2015. Web. 20 Oct 2019.

Vancouver:

Kleinhans DJ. Studies in the synthesis of benzoxazole compounds. [Internet] [Doctoral dissertation]. Stellenbosch University; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10019.1/97900.

Council of Science Editors:

Kleinhans DJ. Studies in the synthesis of benzoxazole compounds. [Doctoral Dissertation]. Stellenbosch University; 2015. Available from: http://hdl.handle.net/10019.1/97900

30. Grenet, Erwann. Cyclisation de Nazarov torquosélective assistée par un sulfoxyde chiral : élaboration stéréocontrôlée d'oxycyclopentanes polysubstitués : Torquoselective Nazarov cyclization assisted by a chiral sulfoxide : stereocontroled synthesis of polysubstituted cyclopentenes.

Degree: Docteur es, Ingénierie biomoléculaire, 2016, Montpellier

Ce travail a été consacré à l’utilisation d’un sulfoxyde chiral pour effectuer une réaction de cyclisation polarisée de Nazarov asymétrique. Une méthodologie mettant en jeu… (more)

Subjects/Keywords: Sulfoxyde chiral; Réaction de Nazarov; Torquosélectivité; Synthèse asymétrique; Chiral sulfoxide; Nazarov reaction; Torquoselectivity; Asymmetric synthesis

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

APA (6th Edition):

Grenet, E. (2016). Cyclisation de Nazarov torquosélective assistée par un sulfoxyde chiral : élaboration stéréocontrôlée d'oxycyclopentanes polysubstitués : Torquoselective Nazarov cyclization assisted by a chiral sulfoxide : stereocontroled synthesis of polysubstituted cyclopentenes. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2016MONTS004

Chicago Manual of Style (16th Edition):

Grenet, Erwann. “Cyclisation de Nazarov torquosélective assistée par un sulfoxyde chiral : élaboration stéréocontrôlée d'oxycyclopentanes polysubstitués : Torquoselective Nazarov cyclization assisted by a chiral sulfoxide : stereocontroled synthesis of polysubstituted cyclopentenes.” 2016. Doctoral Dissertation, Montpellier. Accessed October 20, 2019. http://www.theses.fr/2016MONTS004.

MLA Handbook (7th Edition):

Grenet, Erwann. “Cyclisation de Nazarov torquosélective assistée par un sulfoxyde chiral : élaboration stéréocontrôlée d'oxycyclopentanes polysubstitués : Torquoselective Nazarov cyclization assisted by a chiral sulfoxide : stereocontroled synthesis of polysubstituted cyclopentenes.” 2016. Web. 20 Oct 2019.

Vancouver:

Grenet E. Cyclisation de Nazarov torquosélective assistée par un sulfoxyde chiral : élaboration stéréocontrôlée d'oxycyclopentanes polysubstitués : Torquoselective Nazarov cyclization assisted by a chiral sulfoxide : stereocontroled synthesis of polysubstituted cyclopentenes. [Internet] [Doctoral dissertation]. Montpellier; 2016. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2016MONTS004.

Council of Science Editors:

Grenet E. Cyclisation de Nazarov torquosélective assistée par un sulfoxyde chiral : élaboration stéréocontrôlée d'oxycyclopentanes polysubstitués : Torquoselective Nazarov cyclization assisted by a chiral sulfoxide : stereocontroled synthesis of polysubstituted cyclopentenes. [Doctoral Dissertation]. Montpellier; 2016. Available from: http://www.theses.fr/2016MONTS004

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