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You searched for subject:(cycloaddition). Showing records 1 – 30 of 44 total matches.

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1. GUTI?RREZ COLLAR, AAR?N. Enantioselective organocatalytic cycloaddition reactions between enolisable anhydrides and imines.

Degree: School of Chemistry. Discipline of Chemistry, 2019, Trinity College Dublin

Cycloaddition reactions between enolisable anhydrides and imines have long been known as excellent tools for the synthesis of natural products. The racemic version is well… (more)

Subjects/Keywords: Cycloaddition reactions

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APA (6th Edition):

GUTI?RREZ COLLAR, A. (2019). Enantioselective organocatalytic cycloaddition reactions between enolisable anhydrides and imines. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/88782

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):

GUTI?RREZ COLLAR, AAR?N. “Enantioselective organocatalytic cycloaddition reactions between enolisable anhydrides and imines.” 2019. Thesis, Trinity College Dublin. Accessed October 17, 2019. http://hdl.handle.net/2262/88782.

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

MLA Handbook (7th Edition):

GUTI?RREZ COLLAR, AAR?N. “Enantioselective organocatalytic cycloaddition reactions between enolisable anhydrides and imines.” 2019. Web. 17 Oct 2019.

Vancouver:

GUTI?RREZ COLLAR A. Enantioselective organocatalytic cycloaddition reactions between enolisable anhydrides and imines. [Internet] [Thesis]. Trinity College Dublin; 2019. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2262/88782.

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

Council of Science Editors:

GUTI?RREZ COLLAR A. Enantioselective organocatalytic cycloaddition reactions between enolisable anhydrides and imines. [Thesis]. Trinity College Dublin; 2019. Available from: http://hdl.handle.net/2262/88782

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


University of Guelph

2. Petko, Dina. Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition .

Degree: 2018, University of Guelph

 Synthetic organic chemistry is an integral part of pharmaceutical design and development, which builds upon past literature to create molecules that mimic nature. The synthesis… (more)

Subjects/Keywords: Ruthenium; catalyzed; cycloaddition; Diels-Alder

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APA (6th Edition):

Petko, D. (2018). Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094

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):

Petko, Dina. “Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition .” 2018. Thesis, University of Guelph. Accessed October 17, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094.

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

MLA Handbook (7th Edition):

Petko, Dina. “Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition .” 2018. Web. 17 Oct 2019.

Vancouver:

Petko D. Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition . [Internet] [Thesis]. University of Guelph; 2018. [cited 2019 Oct 17]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094.

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

Council of Science Editors:

Petko D. Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition . [Thesis]. University of Guelph; 2018. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094

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

3. LOCKETT-WALTERS, BRUCE. The Tamura Cycloaddition: Mechanism and Enantiocontrol.

Degree: School of Chemistry. Discipline of Chemistry, 2019, Trinity College Dublin

 This thesis documents attempts to employ succinimide derivatives as ?anhydride surrogates? in the organocatalytic cycloaddition between aryl succinic anhydrides and various electrophiles previously developed in… (more)

Subjects/Keywords: Succinimide derivatives; Tamura cycloaddition

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APA (6th Edition):

LOCKETT-WALTERS, B. (2019). The Tamura Cycloaddition: Mechanism and Enantiocontrol. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/88750

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):

LOCKETT-WALTERS, BRUCE. “The Tamura Cycloaddition: Mechanism and Enantiocontrol.” 2019. Thesis, Trinity College Dublin. Accessed October 17, 2019. http://hdl.handle.net/2262/88750.

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

MLA Handbook (7th Edition):

LOCKETT-WALTERS, BRUCE. “The Tamura Cycloaddition: Mechanism and Enantiocontrol.” 2019. Web. 17 Oct 2019.

Vancouver:

LOCKETT-WALTERS B. The Tamura Cycloaddition: Mechanism and Enantiocontrol. [Internet] [Thesis]. Trinity College Dublin; 2019. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2262/88750.

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

Council of Science Editors:

LOCKETT-WALTERS B. The Tamura Cycloaddition: Mechanism and Enantiocontrol. [Thesis]. Trinity College Dublin; 2019. Available from: http://hdl.handle.net/2262/88750

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


University of Ottawa

4. Rochon, Alexandra. Cycloaddition Reactions of Ni(0) Difluorocarbene Complexes: Investigating the Formation of Various Perfluorometallacycles .

Degree: 2019, University of Ottawa

 Formation of carbon–fluorine and carbon–fluoroalkyl bonds via transition metal complexes represents an efficient synthetic route towards a wide array of valuable fluorinated organic compounds and… (more)

Subjects/Keywords: Cycloaddition reactions; Carbon-fluoroalkyl; Carbon-fluorine

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APA (6th Edition):

Rochon, A. (2019). Cycloaddition Reactions of Ni(0) Difluorocarbene Complexes: Investigating the Formation of Various Perfluorometallacycles . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/39026

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):

Rochon, Alexandra. “Cycloaddition Reactions of Ni(0) Difluorocarbene Complexes: Investigating the Formation of Various Perfluorometallacycles .” 2019. Thesis, University of Ottawa. Accessed October 17, 2019. http://hdl.handle.net/10393/39026.

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

MLA Handbook (7th Edition):

Rochon, Alexandra. “Cycloaddition Reactions of Ni(0) Difluorocarbene Complexes: Investigating the Formation of Various Perfluorometallacycles .” 2019. Web. 17 Oct 2019.

Vancouver:

Rochon A. Cycloaddition Reactions of Ni(0) Difluorocarbene Complexes: Investigating the Formation of Various Perfluorometallacycles . [Internet] [Thesis]. University of Ottawa; 2019. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10393/39026.

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

Council of Science Editors:

Rochon A. Cycloaddition Reactions of Ni(0) Difluorocarbene Complexes: Investigating the Formation of Various Perfluorometallacycles . [Thesis]. University of Ottawa; 2019. Available from: http://hdl.handle.net/10393/39026

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


Florida Atlantic University

5. St.Germain, Elijah. Synthesis and Bioactivity Investigation of Bridged Bicyclic Compounds and a Mechanistic Investigation of a Propargyl Hydrazine Cycloaddition Catalyzed by an Ammonium Salt.

Degree: 2018, Florida Atlantic University

We report the development of a general route to the synthesis of [4.3.1], [3.3.1], an especially [3.2.1] bicyclic compounds structurally related to vitisinol D, a… (more)

Subjects/Keywords: Bicyclic compounds.; Ammonium salts.; Cycloaddition Reaction.

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APA (6th Edition):

St.Germain, E. (2018). Synthesis and Bioactivity Investigation of Bridged Bicyclic Compounds and a Mechanistic Investigation of a Propargyl Hydrazine Cycloaddition Catalyzed by an Ammonium Salt. (Thesis). Florida Atlantic University. Retrieved from http://fau.digital.flvc.org/islandora/object/fau:40756

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):

St.Germain, Elijah. “Synthesis and Bioactivity Investigation of Bridged Bicyclic Compounds and a Mechanistic Investigation of a Propargyl Hydrazine Cycloaddition Catalyzed by an Ammonium Salt.” 2018. Thesis, Florida Atlantic University. Accessed October 17, 2019. http://fau.digital.flvc.org/islandora/object/fau:40756.

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

MLA Handbook (7th Edition):

St.Germain, Elijah. “Synthesis and Bioactivity Investigation of Bridged Bicyclic Compounds and a Mechanistic Investigation of a Propargyl Hydrazine Cycloaddition Catalyzed by an Ammonium Salt.” 2018. Web. 17 Oct 2019.

Vancouver:

St.Germain E. Synthesis and Bioactivity Investigation of Bridged Bicyclic Compounds and a Mechanistic Investigation of a Propargyl Hydrazine Cycloaddition Catalyzed by an Ammonium Salt. [Internet] [Thesis]. Florida Atlantic University; 2018. [cited 2019 Oct 17]. Available from: http://fau.digital.flvc.org/islandora/object/fau:40756.

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

Council of Science Editors:

St.Germain E. Synthesis and Bioactivity Investigation of Bridged Bicyclic Compounds and a Mechanistic Investigation of a Propargyl Hydrazine Cycloaddition Catalyzed by an Ammonium Salt. [Thesis]. Florida Atlantic University; 2018. Available from: http://fau.digital.flvc.org/islandora/object/fau:40756

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


University of Minnesota

6. Xiao, Xiao. The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics.

Degree: PhD, Chemistry, 2019, University of Minnesota

 Polycyclic arenes are an important class of organic molecules with promising semiconducting properties. Their relatively low cost, band-gap tunability, and ease of fabrication render them… (more)

Subjects/Keywords: Cycloaddition; Diels–Alder; HDDA; Polyacene; Polyaromatic

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APA (6th Edition):

Xiao, X. (2019). The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/206228

Chicago Manual of Style (16th Edition):

Xiao, Xiao. “The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics.” 2019. Doctoral Dissertation, University of Minnesota. Accessed October 17, 2019. http://hdl.handle.net/11299/206228.

MLA Handbook (7th Edition):

Xiao, Xiao. “The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics.” 2019. Web. 17 Oct 2019.

Vancouver:

Xiao X. The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/11299/206228.

Council of Science Editors:

Xiao X. The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics. [Doctoral Dissertation]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/206228

7. Bernard, Sabrina. Les mésoioniques : de nouveaux outils pour la chimie bioorthogonale : Mesoionics : new tools for bioorthogonal chemistry.

Degree: Docteur es, Chimie, 2018, Paris Saclay

Notre laboratoire a récemment mis en évidence la réaction de cycloaddition entre les sydnones et les alcynes terminaux ou cycliques. Ces réactions sont bioorthogonales et… (more)

Subjects/Keywords: Chimie bioorthogonale; Mésoioniques; Criblage; Cycloaddition; Relargage; Bioorthogonal chemistry; Mesoionic compounds; Screening; Cycloaddition; Release reactions

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APA (6th Edition):

Bernard, S. (2018). Les mésoioniques : de nouveaux outils pour la chimie bioorthogonale : Mesoionics : new tools for bioorthogonal chemistry. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS289

Chicago Manual of Style (16th Edition):

Bernard, Sabrina. “Les mésoioniques : de nouveaux outils pour la chimie bioorthogonale : Mesoionics : new tools for bioorthogonal chemistry.” 2018. Doctoral Dissertation, Paris Saclay. Accessed October 17, 2019. http://www.theses.fr/2018SACLS289.

MLA Handbook (7th Edition):

Bernard, Sabrina. “Les mésoioniques : de nouveaux outils pour la chimie bioorthogonale : Mesoionics : new tools for bioorthogonal chemistry.” 2018. Web. 17 Oct 2019.

Vancouver:

Bernard S. Les mésoioniques : de nouveaux outils pour la chimie bioorthogonale : Mesoionics : new tools for bioorthogonal chemistry. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2018SACLS289.

Council of Science Editors:

Bernard S. Les mésoioniques : de nouveaux outils pour la chimie bioorthogonale : Mesoionics : new tools for bioorthogonal chemistry. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS289

8. Rouzier, Florian. Synthèse de nouveaux analogues C-glycosidiques d'alpha-galactosylcéramides : couplage des glycolipides à des anticorps spécifiques : Synthesis of new C-glycosidic analogs of alpha-galactosylceramides : glycoconjugates synthesis combining glycolipid and targeting agent.

Degree: Docteur es, Chimie moléculaire et macromoléculaire, 2018, Le Mans

Le sujet de thèse concerne l’immunothérapie induite par des glycolipides synthétiques dont le chef de file est le KRN7000. Ce composé montre une activité à… (more)

Subjects/Keywords: Galactosylcéramides; Vectorisation; C-glycoside; Cycloaddition 1,3-dipolaire; Galactosylceramides; Vectorization; C-glycoside; 1,3-dipolar cycloaddition; 547

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APA (6th Edition):

Rouzier, F. (2018). Synthèse de nouveaux analogues C-glycosidiques d'alpha-galactosylcéramides : couplage des glycolipides à des anticorps spécifiques : Synthesis of new C-glycosidic analogs of alpha-galactosylceramides : glycoconjugates synthesis combining glycolipid and targeting agent. (Doctoral Dissertation). Le Mans. Retrieved from http://www.theses.fr/2018LEMA1027

Chicago Manual of Style (16th Edition):

Rouzier, Florian. “Synthèse de nouveaux analogues C-glycosidiques d'alpha-galactosylcéramides : couplage des glycolipides à des anticorps spécifiques : Synthesis of new C-glycosidic analogs of alpha-galactosylceramides : glycoconjugates synthesis combining glycolipid and targeting agent.” 2018. Doctoral Dissertation, Le Mans. Accessed October 17, 2019. http://www.theses.fr/2018LEMA1027.

MLA Handbook (7th Edition):

Rouzier, Florian. “Synthèse de nouveaux analogues C-glycosidiques d'alpha-galactosylcéramides : couplage des glycolipides à des anticorps spécifiques : Synthesis of new C-glycosidic analogs of alpha-galactosylceramides : glycoconjugates synthesis combining glycolipid and targeting agent.” 2018. Web. 17 Oct 2019.

Vancouver:

Rouzier F. Synthèse de nouveaux analogues C-glycosidiques d'alpha-galactosylcéramides : couplage des glycolipides à des anticorps spécifiques : Synthesis of new C-glycosidic analogs of alpha-galactosylceramides : glycoconjugates synthesis combining glycolipid and targeting agent. [Internet] [Doctoral dissertation]. Le Mans; 2018. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2018LEMA1027.

Council of Science Editors:

Rouzier F. Synthèse de nouveaux analogues C-glycosidiques d'alpha-galactosylcéramides : couplage des glycolipides à des anticorps spécifiques : Synthesis of new C-glycosidic analogs of alpha-galactosylceramides : glycoconjugates synthesis combining glycolipid and targeting agent. [Doctoral Dissertation]. Le Mans; 2018. Available from: http://www.theses.fr/2018LEMA1027

9. Marques, Anne-Sophie. Développement de nouvelles réactions domino initiées par une cyclisation d'iso-Nazarov pour la synthèse de composés polycycliques : Development of iso-Nazarov-initiated domino reactions for the synthesis of polycyclic compounds.

Degree: Docteur es, Chimie, 2018, Paris Saclay

Les molécules polycycliques représentent un défi en synthèse organique en raison de leur complexité moléculaire. Elles sont contenues dans de nombreux produits naturels et font… (more)

Subjects/Keywords: Cycloaddition; Iso-Nazarov; Fer; Électrocyclisation; Polycycles; Cycloaddition; Iso-Nazarov; Iron; Electrocyclisation; Polycycles; 547

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APA (6th Edition):

Marques, A. (2018). Développement de nouvelles réactions domino initiées par une cyclisation d'iso-Nazarov pour la synthèse de composés polycycliques : Development of iso-Nazarov-initiated domino reactions for the synthesis of polycyclic compounds. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLV075

Chicago Manual of Style (16th Edition):

Marques, Anne-Sophie. “Développement de nouvelles réactions domino initiées par une cyclisation d'iso-Nazarov pour la synthèse de composés polycycliques : Development of iso-Nazarov-initiated domino reactions for the synthesis of polycyclic compounds.” 2018. Doctoral Dissertation, Paris Saclay. Accessed October 17, 2019. http://www.theses.fr/2018SACLV075.

MLA Handbook (7th Edition):

Marques, Anne-Sophie. “Développement de nouvelles réactions domino initiées par une cyclisation d'iso-Nazarov pour la synthèse de composés polycycliques : Development of iso-Nazarov-initiated domino reactions for the synthesis of polycyclic compounds.” 2018. Web. 17 Oct 2019.

Vancouver:

Marques A. Développement de nouvelles réactions domino initiées par une cyclisation d'iso-Nazarov pour la synthèse de composés polycycliques : Development of iso-Nazarov-initiated domino reactions for the synthesis of polycyclic compounds. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2018SACLV075.

Council of Science Editors:

Marques A. Développement de nouvelles réactions domino initiées par une cyclisation d'iso-Nazarov pour la synthèse de composés polycycliques : Development of iso-Nazarov-initiated domino reactions for the synthesis of polycyclic compounds. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLV075

10. Perez, Vincent. Synthèses sélectives d’isoxazolines et isoxazoles phosphonates : compétition de C- vs. O-alkylation et cycloadditions d’ynamido-phosphonates : Selective synthesis of isoxazoline- and isoxazole-phosphonates : competition of C- vs. O alkylation and cycloadditions of ynamido phosphonates.

Degree: Docteur es, Chimie, 2017, Paris Saclay

En raison de la vaste gamme d'activités biologiques qu'ils possèdent, les aminophosphonates cycliques ont attiré l’attention des chimistes et des biologistes. La synthèse d’hétérocycles substitués… (more)

Subjects/Keywords: Méthodologie; Aminophosphonates; Alkylation; Cycloaddition; Cyclisation; Oxydation; Methodology; Aminophosphonates; Alkylation; Cycloaddition; Cyclization; Oxidation

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APA (6th Edition):

Perez, V. (2017). Synthèses sélectives d’isoxazolines et isoxazoles phosphonates : compétition de C- vs. O-alkylation et cycloadditions d’ynamido-phosphonates : Selective synthesis of isoxazoline- and isoxazole-phosphonates : competition of C- vs. O alkylation and cycloadditions of ynamido phosphonates. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2017SACLS363

Chicago Manual of Style (16th Edition):

Perez, Vincent. “Synthèses sélectives d’isoxazolines et isoxazoles phosphonates : compétition de C- vs. O-alkylation et cycloadditions d’ynamido-phosphonates : Selective synthesis of isoxazoline- and isoxazole-phosphonates : competition of C- vs. O alkylation and cycloadditions of ynamido phosphonates.” 2017. Doctoral Dissertation, Paris Saclay. Accessed October 17, 2019. http://www.theses.fr/2017SACLS363.

MLA Handbook (7th Edition):

Perez, Vincent. “Synthèses sélectives d’isoxazolines et isoxazoles phosphonates : compétition de C- vs. O-alkylation et cycloadditions d’ynamido-phosphonates : Selective synthesis of isoxazoline- and isoxazole-phosphonates : competition of C- vs. O alkylation and cycloadditions of ynamido phosphonates.” 2017. Web. 17 Oct 2019.

Vancouver:

Perez V. Synthèses sélectives d’isoxazolines et isoxazoles phosphonates : compétition de C- vs. O-alkylation et cycloadditions d’ynamido-phosphonates : Selective synthesis of isoxazoline- and isoxazole-phosphonates : competition of C- vs. O alkylation and cycloadditions of ynamido phosphonates. [Internet] [Doctoral dissertation]. Paris Saclay; 2017. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2017SACLS363.

Council of Science Editors:

Perez V. Synthèses sélectives d’isoxazolines et isoxazoles phosphonates : compétition de C- vs. O-alkylation et cycloadditions d’ynamido-phosphonates : Selective synthesis of isoxazoline- and isoxazole-phosphonates : competition of C- vs. O alkylation and cycloadditions of ynamido phosphonates. [Doctoral Dissertation]. Paris Saclay; 2017. Available from: http://www.theses.fr/2017SACLS363

11. Feraldi-Xypolia, Alexandra. Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés.

Degree: Docteur es, Chimie Organique, 2017, Université Pierre et Marie Curie – Paris VI

L’introduction d’un atome de fluor sur un composé organique peut avoir une influence importante sur les propriétés chimiques et physico-chimiques de ce composé, ainsi qu’à… (more)

Subjects/Keywords: Contraction de cycle; Αlpha-(trifluorométhyl)pyrrolidines; Αlapha-(trifluorométhyl)pipéridines; Aziridinium; Cycloaddition; Alpha – (trifluorométhyl)pyridazines; Ring contraction; Cycloaddition; Trifluoromethyl; 547

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APA (6th Edition):

Feraldi-Xypolia, A. (2017). Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066444

Chicago Manual of Style (16th Edition):

Feraldi-Xypolia, Alexandra. “Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 17, 2019. http://www.theses.fr/2017PA066444.

MLA Handbook (7th Edition):

Feraldi-Xypolia, Alexandra. “Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés.” 2017. Web. 17 Oct 2019.

Vancouver:

Feraldi-Xypolia A. Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2017PA066444.

Council of Science Editors:

Feraldi-Xypolia A. Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066444

12. Buttard, Floris. 3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis.

Degree: Docteur es, Chimie Organique, 2018, Université d'Orléans

Le développement de nouvelles méthodes de synthèse de molécules hétérocycliques originales représente un enjeu actuel majeur en chimie organique. L’objectif est de fournir de nouveaux… (more)

Subjects/Keywords: Chimie hétéroaromatique; Réaction en cascade; Organocatalyse; Addition conjuguée; Cycloaddition; Heteroaromatic chemistry; Domino reactions; Organocatalysis; Conjugate addition; Cycloaddition; 547

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APA (6th Edition):

Buttard, F. (2018). 3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2018ORLE2032

Chicago Manual of Style (16th Edition):

Buttard, Floris. “3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis.” 2018. Doctoral Dissertation, Université d'Orléans. Accessed October 17, 2019. http://www.theses.fr/2018ORLE2032.

MLA Handbook (7th Edition):

Buttard, Floris. “3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis.” 2018. Web. 17 Oct 2019.

Vancouver:

Buttard F. 3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis. [Internet] [Doctoral dissertation]. Université d'Orléans; 2018. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2018ORLE2032.

Council of Science Editors:

Buttard F. 3-Vinyl-1,2,4-triazines comme plateformes bifonctionnelles pour la synthèse de nouvelles structures tétrahydro-[1,6]-naphthyridines : 3-vinyl-1,2,4-triazines as bifunctional platforms towards new tetrahydro-[1,6]-naphthyridines scaffolds synthesis. [Doctoral Dissertation]. Université d'Orléans; 2018. Available from: http://www.theses.fr/2018ORLE2032

13. Kassir, Ahmad. Photochemical approaches for the synthesis of oxygen- and sulphur-containing heterocycles : Approches photochimiques pour la synthèse d'hétérocycles oxygénés et soufrés.

Degree: Docteur es, Chimie, 2018, Paris Saclay

 Les oxétanes sont des cycles à quatre chaînons comportant un atome d’oxygène intracyclique. Le motif oxétane est présent dans la structure de nombreux produits naturels… (more)

Subjects/Keywords: Oxétine; Oxétane; Thiétane; Thiolane; Photochimie; Cycloaddition 2+2; Oxetin; Oxetane; Thietane; Thiolane; Photochemistry; 2+2 cycloaddition

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APA (6th Edition):

Kassir, A. (2018). Photochemical approaches for the synthesis of oxygen- and sulphur-containing heterocycles : Approches photochimiques pour la synthèse d'hétérocycles oxygénés et soufrés. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS065

Chicago Manual of Style (16th Edition):

Kassir, Ahmad. “Photochemical approaches for the synthesis of oxygen- and sulphur-containing heterocycles : Approches photochimiques pour la synthèse d'hétérocycles oxygénés et soufrés.” 2018. Doctoral Dissertation, Paris Saclay. Accessed October 17, 2019. http://www.theses.fr/2018SACLS065.

MLA Handbook (7th Edition):

Kassir, Ahmad. “Photochemical approaches for the synthesis of oxygen- and sulphur-containing heterocycles : Approches photochimiques pour la synthèse d'hétérocycles oxygénés et soufrés.” 2018. Web. 17 Oct 2019.

Vancouver:

Kassir A. Photochemical approaches for the synthesis of oxygen- and sulphur-containing heterocycles : Approches photochimiques pour la synthèse d'hétérocycles oxygénés et soufrés. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2018SACLS065.

Council of Science Editors:

Kassir A. Photochemical approaches for the synthesis of oxygen- and sulphur-containing heterocycles : Approches photochimiques pour la synthèse d'hétérocycles oxygénés et soufrés. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS065

14. Favre, Camille. Novel bioorthogonal chemical reporters and fluorogenic probes for biomolecules imaging : Nouveaux rapporteurs chimiques et sondes fluorogènes bioorthogonaux pour l'imagerie de biomolécules.

Degree: Docteur es, Interface Chimie Biologie, 2019, Bordeaux

L'imagerie de biomolécules, et plus particulièrement des glycanes, au sein d'organismes vivants, représente un incroyable challenge. Cependant, des progrès significatifs ont été réalisés ces dix… (more)

Subjects/Keywords: Chimie bioorthogonale; Sondes fluorogènes; Cycloaddition 1.3-Dipolaire; Cyclooctynes; Composés mésoioniques; Bioorthogonal chemistry; Fluorogenic probes; 1.3-Dipolar cycloaddition; Cyclooctynes; Meosionic compounds

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APA (6th Edition):

Favre, C. (2019). Novel bioorthogonal chemical reporters and fluorogenic probes for biomolecules imaging : Nouveaux rapporteurs chimiques et sondes fluorogènes bioorthogonaux pour l'imagerie de biomolécules. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2019BORD0079

Chicago Manual of Style (16th Edition):

Favre, Camille. “Novel bioorthogonal chemical reporters and fluorogenic probes for biomolecules imaging : Nouveaux rapporteurs chimiques et sondes fluorogènes bioorthogonaux pour l'imagerie de biomolécules.” 2019. Doctoral Dissertation, Bordeaux. Accessed October 17, 2019. http://www.theses.fr/2019BORD0079.

MLA Handbook (7th Edition):

Favre, Camille. “Novel bioorthogonal chemical reporters and fluorogenic probes for biomolecules imaging : Nouveaux rapporteurs chimiques et sondes fluorogènes bioorthogonaux pour l'imagerie de biomolécules.” 2019. Web. 17 Oct 2019.

Vancouver:

Favre C. Novel bioorthogonal chemical reporters and fluorogenic probes for biomolecules imaging : Nouveaux rapporteurs chimiques et sondes fluorogènes bioorthogonaux pour l'imagerie de biomolécules. [Internet] [Doctoral dissertation]. Bordeaux; 2019. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2019BORD0079.

Council of Science Editors:

Favre C. Novel bioorthogonal chemical reporters and fluorogenic probes for biomolecules imaging : Nouveaux rapporteurs chimiques et sondes fluorogènes bioorthogonaux pour l'imagerie de biomolécules. [Doctoral Dissertation]. Bordeaux; 2019. Available from: http://www.theses.fr/2019BORD0079

15. Leleu, Ludovic. Elaboration de librairies de molécules structurellement diversifiées à partir du squelette de l'acide kojique par des méthodes de synthèse micro-ondes et de flux continu : Elaboration of molecules' libraries structurelly diversified from kojic acid skeleton by microwave and continuous flow synthesis methodologies.

Degree: Docteur es, Chimie Moléculaire, 2017, Paris Sciences et Lettres

La structure de l’acide kojique et sa réactivité permet d’effectuer des transformations conduisant à la synthèse de composés polycycliques différents et structurellement très diversifiés. Ces… (more)

Subjects/Keywords: Dérivés d'acide kojique; Cycloaddition [5+2]; Cycloaddition tandem [5 + 2]/[4 + 2]; Flux continu; Micro-Ondes; Kojic acid derivatives; [5+2] cycloaddition; [5 + 2]/[4 + 2] tandem cycloaddition; Continuous flow; Microwave

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APA (6th Edition):

Leleu, L. (2017). Elaboration de librairies de molécules structurellement diversifiées à partir du squelette de l'acide kojique par des méthodes de synthèse micro-ondes et de flux continu : Elaboration of molecules' libraries structurelly diversified from kojic acid skeleton by microwave and continuous flow synthesis methodologies. (Doctoral Dissertation). Paris Sciences et Lettres. Retrieved from http://www.theses.fr/2017PSLEC005

Chicago Manual of Style (16th Edition):

Leleu, Ludovic. “Elaboration de librairies de molécules structurellement diversifiées à partir du squelette de l'acide kojique par des méthodes de synthèse micro-ondes et de flux continu : Elaboration of molecules' libraries structurelly diversified from kojic acid skeleton by microwave and continuous flow synthesis methodologies.” 2017. Doctoral Dissertation, Paris Sciences et Lettres. Accessed October 17, 2019. http://www.theses.fr/2017PSLEC005.

MLA Handbook (7th Edition):

Leleu, Ludovic. “Elaboration de librairies de molécules structurellement diversifiées à partir du squelette de l'acide kojique par des méthodes de synthèse micro-ondes et de flux continu : Elaboration of molecules' libraries structurelly diversified from kojic acid skeleton by microwave and continuous flow synthesis methodologies.” 2017. Web. 17 Oct 2019.

Vancouver:

Leleu L. Elaboration de librairies de molécules structurellement diversifiées à partir du squelette de l'acide kojique par des méthodes de synthèse micro-ondes et de flux continu : Elaboration of molecules' libraries structurelly diversified from kojic acid skeleton by microwave and continuous flow synthesis methodologies. [Internet] [Doctoral dissertation]. Paris Sciences et Lettres; 2017. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2017PSLEC005.

Council of Science Editors:

Leleu L. Elaboration de librairies de molécules structurellement diversifiées à partir du squelette de l'acide kojique par des méthodes de synthèse micro-ondes et de flux continu : Elaboration of molecules' libraries structurelly diversified from kojic acid skeleton by microwave and continuous flow synthesis methodologies. [Doctoral Dissertation]. Paris Sciences et Lettres; 2017. Available from: http://www.theses.fr/2017PSLEC005

16. CLAVEAU, ROMAIN. Development of novel organocatalysts towards the kinetic and dynamic resolution of chiral enolisable anhydrides.

Degree: School of Chemistry. Discipline of Chemistry, 2018, Trinity College Dublin

 In this thesis we explore the possibilities offered by the bifunctional properties of a series of organocatalysts derived from cinchona alkaloids for the promotion of… (more)

Subjects/Keywords: (dynamic) kinetic resolution; cycloaddition reaction; enolisable anhydrides; diastereoselectivity; enantioselectivity

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APA (6th Edition):

CLAVEAU, R. (2018). Development of novel organocatalysts towards the kinetic and dynamic resolution of chiral enolisable anhydrides. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/85201

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):

CLAVEAU, ROMAIN. “Development of novel organocatalysts towards the kinetic and dynamic resolution of chiral enolisable anhydrides.” 2018. Thesis, Trinity College Dublin. Accessed October 17, 2019. http://hdl.handle.net/2262/85201.

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

MLA Handbook (7th Edition):

CLAVEAU, ROMAIN. “Development of novel organocatalysts towards the kinetic and dynamic resolution of chiral enolisable anhydrides.” 2018. Web. 17 Oct 2019.

Vancouver:

CLAVEAU R. Development of novel organocatalysts towards the kinetic and dynamic resolution of chiral enolisable anhydrides. [Internet] [Thesis]. Trinity College Dublin; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2262/85201.

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

Council of Science Editors:

CLAVEAU R. Development of novel organocatalysts towards the kinetic and dynamic resolution of chiral enolisable anhydrides. [Thesis]. Trinity College Dublin; 2018. Available from: http://hdl.handle.net/2262/85201

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


University of Michigan

17. Ferguson, Kyle. A New Decarboxylase: A Mechanistic Characterization of PrFMN Decarboxylase FDC1.

Degree: PhD, Chemistry, 2018, University of Michigan

 The large number of inexpensive carboxylic acids found in nature has spurred research to convert carboxylic acids to an assortment of other functional groups for… (more)

Subjects/Keywords: FDC1 Decarboxylase; PrFMN; Enzymatic 1,3 Dipolar Cycloaddition; Chemistry; Science

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APA (6th Edition):

Ferguson, K. (2018). A New Decarboxylase: A Mechanistic Characterization of PrFMN Decarboxylase FDC1. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/144153

Chicago Manual of Style (16th Edition):

Ferguson, Kyle. “A New Decarboxylase: A Mechanistic Characterization of PrFMN Decarboxylase FDC1.” 2018. Doctoral Dissertation, University of Michigan. Accessed October 17, 2019. http://hdl.handle.net/2027.42/144153.

MLA Handbook (7th Edition):

Ferguson, Kyle. “A New Decarboxylase: A Mechanistic Characterization of PrFMN Decarboxylase FDC1.” 2018. Web. 17 Oct 2019.

Vancouver:

Ferguson K. A New Decarboxylase: A Mechanistic Characterization of PrFMN Decarboxylase FDC1. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2027.42/144153.

Council of Science Editors:

Ferguson K. A New Decarboxylase: A Mechanistic Characterization of PrFMN Decarboxylase FDC1. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/144153

18. Salacz, Laura. Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis.

Degree: Docteur es, Chimie, 2018, Université de Strasbourg

Ces travaux de thèse ont permis, au cours de deux projets, de s’attacher à la synthèse de structures complexes au moyen de réaction en cascade… (more)

Subjects/Keywords: Tropone; Cycloaddition carbonylative; Cyclohydrocarbonylation; Réaction en cascade; Rhodium; Hydroformylation désymétrisante; Aspidosperma; Tropone; Carbonylative cycloaddition; Cyclohydrocarbonylation; Cascade reactions; Rhodium; Dessymmetrising hydroformylation; Aspidosperma; 541.3

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APA (6th Edition):

Salacz, L. (2018). Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAF034

Chicago Manual of Style (16th Edition):

Salacz, Laura. “Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed October 17, 2019. http://www.theses.fr/2018STRAF034.

MLA Handbook (7th Edition):

Salacz, Laura. “Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis.” 2018. Web. 17 Oct 2019.

Vancouver:

Salacz L. Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2018STRAF034.

Council of Science Editors:

Salacz L. Synthèse de structures complexes par réactions en cascade et catalyse au rhodium : Synthesis of complex structures by means of cascade reactions and rhodium catalysis. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAF034

19. Chang, Zong. Photochemical Syntheses of Functionalized Complex Cyclobutane Derivatives : Synthèse photochimique de dérivés cyclobutaniques complexes fonctionnalisés.

Degree: Docteur es, Chimie, 2018, Paris Saclay

 Les transformations photochimiques sont des outils puissants pour créer de la diversité moléculaires à partir de substrats facilement accessibles; elles requièrent le réactif le plus… (more)

Subjects/Keywords: Cycloaddition [2+2] photochimique; Réactions domino; Réactions type SN2; Cyclobutane; Β-Acides aminés; Photochimie; Cyclobutane; Domino reactions; Β-Amino acids; Photochemical [2+2] cycloaddition; SN2-Type reactions; Photochemistry

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APA (6th Edition):

Chang, Z. (2018). Photochemical Syntheses of Functionalized Complex Cyclobutane Derivatives : Synthèse photochimique de dérivés cyclobutaniques complexes fonctionnalisés. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS420

Chicago Manual of Style (16th Edition):

Chang, Zong. “Photochemical Syntheses of Functionalized Complex Cyclobutane Derivatives : Synthèse photochimique de dérivés cyclobutaniques complexes fonctionnalisés.” 2018. Doctoral Dissertation, Paris Saclay. Accessed October 17, 2019. http://www.theses.fr/2018SACLS420.

MLA Handbook (7th Edition):

Chang, Zong. “Photochemical Syntheses of Functionalized Complex Cyclobutane Derivatives : Synthèse photochimique de dérivés cyclobutaniques complexes fonctionnalisés.” 2018. Web. 17 Oct 2019.

Vancouver:

Chang Z. Photochemical Syntheses of Functionalized Complex Cyclobutane Derivatives : Synthèse photochimique de dérivés cyclobutaniques complexes fonctionnalisés. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2018SACLS420.

Council of Science Editors:

Chang Z. Photochemical Syntheses of Functionalized Complex Cyclobutane Derivatives : Synthèse photochimique de dérivés cyclobutaniques complexes fonctionnalisés. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS420

20. Tangara, Salia. Synthèse d'aziridinyl iminosucres à partir de nitrones et évaluation de leur activité inhibitrice de glycosidases : Synthesis of aziridinyl iminosugars from nitrones and evaluation of their glycosidase inhibitory activities.

Degree: Docteur es, Chimie organique, 2018, Grenoble Alpes

Notre équipe a récemment décrit la synthèse de nouveaux iminosucres de type indolizidines et quinolizidines, qui se sont avérés être de puissants inhibiteurs sélectifs d’α-glucosidases… (more)

Subjects/Keywords: Nitrones dérivées de sucres; Cycloaddition 1.3-Dipolaire; Réarrangement de Baldwin; Aziridinyl iminosucres; Inhibiteurs de glycosidases; Carbohydrate-Derived nitrones; 1.3-Dipolar cycloaddition; Baldwin rearrangement; Aziridinyl iminosugars; Glycosidase inhibitors; 540

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APA (6th Edition):

Tangara, S. (2018). Synthèse d'aziridinyl iminosucres à partir de nitrones et évaluation de leur activité inhibitrice de glycosidases : Synthesis of aziridinyl iminosugars from nitrones and evaluation of their glycosidase inhibitory activities. (Doctoral Dissertation). Grenoble Alpes. Retrieved from http://www.theses.fr/2018GREAV053

Chicago Manual of Style (16th Edition):

Tangara, Salia. “Synthèse d'aziridinyl iminosucres à partir de nitrones et évaluation de leur activité inhibitrice de glycosidases : Synthesis of aziridinyl iminosugars from nitrones and evaluation of their glycosidase inhibitory activities.” 2018. Doctoral Dissertation, Grenoble Alpes. Accessed October 17, 2019. http://www.theses.fr/2018GREAV053.

MLA Handbook (7th Edition):

Tangara, Salia. “Synthèse d'aziridinyl iminosucres à partir de nitrones et évaluation de leur activité inhibitrice de glycosidases : Synthesis of aziridinyl iminosugars from nitrones and evaluation of their glycosidase inhibitory activities.” 2018. Web. 17 Oct 2019.

Vancouver:

Tangara S. Synthèse d'aziridinyl iminosucres à partir de nitrones et évaluation de leur activité inhibitrice de glycosidases : Synthesis of aziridinyl iminosugars from nitrones and evaluation of their glycosidase inhibitory activities. [Internet] [Doctoral dissertation]. Grenoble Alpes; 2018. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2018GREAV053.

Council of Science Editors:

Tangara S. Synthèse d'aziridinyl iminosucres à partir de nitrones et évaluation de leur activité inhibitrice de glycosidases : Synthesis of aziridinyl iminosugars from nitrones and evaluation of their glycosidase inhibitory activities. [Doctoral Dissertation]. Grenoble Alpes; 2018. Available from: http://www.theses.fr/2018GREAV053

21. WANG YANONG. MEDIUM-SIZED RING SYNTHESIS VIA PALLADIUM-CATALYZED CYCLOADDITION.

Degree: 2018, National University of Singapore

Subjects/Keywords: medium-sized rings; [6+4] cycloaddition; [8+4] cycloaddition; palladium; heterocycles; homogeneous catalysis

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APA (6th Edition):

YANONG, W. (2018). MEDIUM-SIZED RING SYNTHESIS VIA PALLADIUM-CATALYZED CYCLOADDITION. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/151083

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):

YANONG, WANG. “MEDIUM-SIZED RING SYNTHESIS VIA PALLADIUM-CATALYZED CYCLOADDITION.” 2018. Thesis, National University of Singapore. Accessed October 17, 2019. http://scholarbank.nus.edu.sg/handle/10635/151083.

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

MLA Handbook (7th Edition):

YANONG, WANG. “MEDIUM-SIZED RING SYNTHESIS VIA PALLADIUM-CATALYZED CYCLOADDITION.” 2018. Web. 17 Oct 2019.

Vancouver:

YANONG W. MEDIUM-SIZED RING SYNTHESIS VIA PALLADIUM-CATALYZED CYCLOADDITION. [Internet] [Thesis]. National University of Singapore; 2018. [cited 2019 Oct 17]. Available from: http://scholarbank.nus.edu.sg/handle/10635/151083.

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

Council of Science Editors:

YANONG W. MEDIUM-SIZED RING SYNTHESIS VIA PALLADIUM-CATALYZED CYCLOADDITION. [Thesis]. National University of Singapore; 2018. Available from: http://scholarbank.nus.edu.sg/handle/10635/151083

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

22. Laugeois, Maxime. Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis.

Degree: Docteur es, Chimie organique, 2017, Université Pierre et Marie Curie – Paris VI

Ce manuscrit présente le développement de nouvelles réactions de cycloaddition [3+2] palladocatalysées entre des vinylcyclopropanes électro-appauvris et diverses espèces dipolarophiles. La première partie de ces… (more)

Subjects/Keywords: Cycloaddition [3+2]; Palladium; Vinylcyclopropanes; Désaromatisation; Métallo-organocatalyse; Catalyse asymétrique; Palladium; Asymmetric catalysis; Vinylcyclopropanes; 547

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APA (6th Edition):

Laugeois, M. (2017). Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066353

Chicago Manual of Style (16th Edition):

Laugeois, Maxime. “Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed October 17, 2019. http://www.theses.fr/2017PA066353.

MLA Handbook (7th Edition):

Laugeois, Maxime. “Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis.” 2017. Web. 17 Oct 2019.

Vancouver:

Laugeois M. Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2017PA066353.

Council of Science Editors:

Laugeois M. Réactions de cycloadditions stéréosélectives originales reposant sur l'utilisation de vinylcyclopropanes électro-appauvris et la catalyse au palladium(0) : Original stereoselective cycloaddition reactions based on the use of electron-poor vinylcyclopropanes and palladium(0) calaysis. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066353

23. Ríos Gutiérrez, Mª del Mar. Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory.

Degree: 2018, TDX

 After the first classification of [3+2] cycloaddition (32CA) reactions into zw-type and pr-type reactions, established in 2014, the structure and reactivity of the most important… (more)

Subjects/Keywords: Molecular Electron Density Theory; [3+2] Cycloaddition Reactions; Molecular Mechanisms; Theoretical Organic Chemistry; Organic Reactivity

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

APA (6th Edition):

Ríos Gutiérrez, M. d. M. (2018). Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory. (Thesis). TDX. Retrieved from http://hdl.handle.net/10803/580543

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):

Ríos Gutiérrez, Mª del Mar. “Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory.” 2018. Thesis, TDX. Accessed October 17, 2019. http://hdl.handle.net/10803/580543.

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

MLA Handbook (7th Edition):

Ríos Gutiérrez, Mª del Mar. “Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory.” 2018. Web. 17 Oct 2019.

Vancouver:

Ríos Gutiérrez MdM. Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory. [Internet] [Thesis]. TDX; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10803/580543.

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

Council of Science Editors:

Ríos Gutiérrez MdM. Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory. [Thesis]. TDX; 2018. Available from: http://hdl.handle.net/10803/580543

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

24. Ríos Gutiérrez, Mª del Mar. Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory.

Degree: 2018, TDX

 After the first classification of [3+2] cycloaddition (32CA) reactions into zw-type and pr-type reactions, established in 2014, the structure and reactivity of the most important… (more)

Subjects/Keywords: Molecular Electron Density Theory; [3+2] Cycloaddition Reactions; Molecular Mechanisms; Theoretical Organic Chemistry; Organic Reactivity

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

APA (6th Edition):

Ríos Gutiérrez, M. d. M. (2018). Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory. (Thesis). TDX. Retrieved from http://hdl.handle.net/10803/571976

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):

Ríos Gutiérrez, Mª del Mar. “Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory.” 2018. Thesis, TDX. Accessed October 17, 2019. http://hdl.handle.net/10803/571976.

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

MLA Handbook (7th Edition):

Ríos Gutiérrez, Mª del Mar. “Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory.” 2018. Web. 17 Oct 2019.

Vancouver:

Ríos Gutiérrez MdM. Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory. [Internet] [Thesis]. TDX; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10803/571976.

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

Council of Science Editors:

Ríos Gutiérrez MdM. Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory. [Thesis]. TDX; 2018. Available from: http://hdl.handle.net/10803/571976

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


University of Lund

25. Peterson, Kristoffer. Molecular basis for galectin-ligand interactions : Design, synthesis and analysis of ligands.

Degree: 2018, University of Lund

 Galectins are a class of β-galactoside-binding proteins that bind glycoconjugates and have been implicated in cancer, regulation of immunity and inflammation. Design and synthesis have… (more)

Subjects/Keywords: Organisk kemi; Galectin; Structure-based design; Thiodigalactoside; Huisgen 1,3-dipolar cycloaddition; Protein-ligand binding interactions

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APA (6th Edition):

Peterson, K. (2018). Molecular basis for galectin-ligand interactions : Design, synthesis and analysis of ligands. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/777b2fa7-2293-453b-9771-0f0ab6f6a6d2 ; http://portal.research.lu.se/ws/files/38414625/Thesis.pdf

Chicago Manual of Style (16th Edition):

Peterson, Kristoffer. “Molecular basis for galectin-ligand interactions : Design, synthesis and analysis of ligands.” 2018. Doctoral Dissertation, University of Lund. Accessed October 17, 2019. http://lup.lub.lu.se/record/777b2fa7-2293-453b-9771-0f0ab6f6a6d2 ; http://portal.research.lu.se/ws/files/38414625/Thesis.pdf.

MLA Handbook (7th Edition):

Peterson, Kristoffer. “Molecular basis for galectin-ligand interactions : Design, synthesis and analysis of ligands.” 2018. Web. 17 Oct 2019.

Vancouver:

Peterson K. Molecular basis for galectin-ligand interactions : Design, synthesis and analysis of ligands. [Internet] [Doctoral dissertation]. University of Lund; 2018. [cited 2019 Oct 17]. Available from: http://lup.lub.lu.se/record/777b2fa7-2293-453b-9771-0f0ab6f6a6d2 ; http://portal.research.lu.se/ws/files/38414625/Thesis.pdf.

Council of Science Editors:

Peterson K. Molecular basis for galectin-ligand interactions : Design, synthesis and analysis of ligands. [Doctoral Dissertation]. University of Lund; 2018. Available from: http://lup.lub.lu.se/record/777b2fa7-2293-453b-9771-0f0ab6f6a6d2 ; http://portal.research.lu.se/ws/files/38414625/Thesis.pdf


Universitat de Valencia

26. Ríos Gutiérrez, Mª del Mar. Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory .

Degree: 2018, Universitat de Valencia

 Después de la primera clasificación de las reacciones 32CA en reacciones de tipo zw y pr, establecidas en el año 2014, la estructura y reactividad… (more)

Subjects/Keywords: Molecular Electron Density Theory; [3+2] Cycloaddition Reactions; Molecular Mechanisms; Theoretical Organic Chemistry; Organic Reactivity

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

APA (6th Edition):

Ríos Gutiérrez, M. d. M. (2018). Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/65482

Chicago Manual of Style (16th Edition):

Ríos Gutiérrez, Mª del Mar. “Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory .” 2018. Doctoral Dissertation, Universitat de Valencia. Accessed October 17, 2019. http://hdl.handle.net/10550/65482.

MLA Handbook (7th Edition):

Ríos Gutiérrez, Mª del Mar. “Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory .” 2018. Web. 17 Oct 2019.

Vancouver:

Ríos Gutiérrez MdM. Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10550/65482.

Council of Science Editors:

Ríos Gutiérrez MdM. Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory . [Doctoral Dissertation]. Universitat de Valencia; 2018. Available from: http://hdl.handle.net/10550/65482


Universidad de Extremadura

27. García de la Concepción, Juan. Estudio teórico-experimental de la reactividad 1,3-dipolar de tioisomünchnonas bicíclicas .

Degree: 2019, Universidad de Extremadura

 La reacción de cicloadición 1,3-dipolar se introdujo en 1960 como un método general de síntesis de anillos de cinco miembros y, en la actualidad, constituye… (more)

Subjects/Keywords: Cicloadición 1,3-dipolar; Heterociclos mesoiónicos; Química computacional; 1,3-Dipolar cycloaddition; Mesoionic heterocycles; Computational chemistry

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

APA (6th Edition):

García de la Concepción, J. (2019). Estudio teórico-experimental de la reactividad 1,3-dipolar de tioisomünchnonas bicíclicas . (Thesis). Universidad de Extremadura. Retrieved from http://hdl.handle.net/10662/8634

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):

García de la Concepción, Juan. “Estudio teórico-experimental de la reactividad 1,3-dipolar de tioisomünchnonas bicíclicas .” 2019. Thesis, Universidad de Extremadura. Accessed October 17, 2019. http://hdl.handle.net/10662/8634.

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

MLA Handbook (7th Edition):

García de la Concepción, Juan. “Estudio teórico-experimental de la reactividad 1,3-dipolar de tioisomünchnonas bicíclicas .” 2019. Web. 17 Oct 2019.

Vancouver:

García de la Concepción J. Estudio teórico-experimental de la reactividad 1,3-dipolar de tioisomünchnonas bicíclicas . [Internet] [Thesis]. Universidad de Extremadura; 2019. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10662/8634.

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

Council of Science Editors:

García de la Concepción J. Estudio teórico-experimental de la reactividad 1,3-dipolar de tioisomünchnonas bicíclicas . [Thesis]. Universidad de Extremadura; 2019. Available from: http://hdl.handle.net/10662/8634

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


NSYSU

28. Chen, Yi-siang. Boroxole Modified Microarray for Glycoprotein Immobilization and Glycan profiling.

Degree: Master, Chemistry, 2018, NSYSU

 The glycosyl group of glycoprotein influences proteinâs structure, stability and functional. Not only do the cell identification on the surface of cell membrane, but also… (more)

Subjects/Keywords: strain-promoted azide-alkyne cycloaddition; tosyl; boroxole; glycoprotein microarray; Epoxy group array

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

APA (6th Edition):

Chen, Y. (2018). Boroxole Modified Microarray for Glycoprotein Immobilization and Glycan profiling. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0721118-141535

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):

Chen, Yi-siang. “Boroxole Modified Microarray for Glycoprotein Immobilization and Glycan profiling.” 2018. Thesis, NSYSU. Accessed October 17, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0721118-141535.

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

MLA Handbook (7th Edition):

Chen, Yi-siang. “Boroxole Modified Microarray for Glycoprotein Immobilization and Glycan profiling.” 2018. Web. 17 Oct 2019.

Vancouver:

Chen Y. Boroxole Modified Microarray for Glycoprotein Immobilization and Glycan profiling. [Internet] [Thesis]. NSYSU; 2018. [cited 2019 Oct 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0721118-141535.

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

Council of Science Editors:

Chen Y. Boroxole Modified Microarray for Glycoprotein Immobilization and Glycan profiling. [Thesis]. NSYSU; 2018. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0721118-141535

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

29. GERMAINE KOK PUI YANN. SYNTHESIS OF N-HETEROCYCLES WITH ACTIVATED ISOCYANIDES.

Degree: 2018, National University of Singapore

Subjects/Keywords: isocyanoacetates; cycloaddition; pyrroles; tetrahydropyrimidine; catalysis; methodology

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

APA (6th Edition):

YANN, G. K. P. (2018). SYNTHESIS OF N-HETEROCYCLES WITH ACTIVATED ISOCYANIDES. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/151876

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):

YANN, GERMAINE KOK PUI. “SYNTHESIS OF N-HETEROCYCLES WITH ACTIVATED ISOCYANIDES.” 2018. Thesis, National University of Singapore. Accessed October 17, 2019. http://scholarbank.nus.edu.sg/handle/10635/151876.

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

MLA Handbook (7th Edition):

YANN, GERMAINE KOK PUI. “SYNTHESIS OF N-HETEROCYCLES WITH ACTIVATED ISOCYANIDES.” 2018. Web. 17 Oct 2019.

Vancouver:

YANN GKP. SYNTHESIS OF N-HETEROCYCLES WITH ACTIVATED ISOCYANIDES. [Internet] [Thesis]. National University of Singapore; 2018. [cited 2019 Oct 17]. Available from: http://scholarbank.nus.edu.sg/handle/10635/151876.

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

Council of Science Editors:

YANN GKP. SYNTHESIS OF N-HETEROCYCLES WITH ACTIVATED ISOCYANIDES. [Thesis]. National University of Singapore; 2018. Available from: http://scholarbank.nus.edu.sg/handle/10635/151876

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


East Tennessee State University

30. Kalu, Chimdi Eke. Synthesis and Evaluation of 1,2,4-oxadiazolidinones: The Search for A Potential Non-β-lactam β-lactamase Inhibitors.

Degree: MS, Chemistry, 2019, East Tennessee State University

  β-lactam antibiotics have been the most widely used drug of choice to combat infectious disease caused by bacteria. Unfortunately, their effectiveness is drastically threatened… (more)

Subjects/Keywords: Antibiotic resistance; β-Lactamases inhibitors; Nitrones; Cycloaddition Reaction; Oxadiazolidinones and Enzyme kinetics; Organic Chemistry

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

APA (6th Edition):

Kalu, C. E. (2019). Synthesis and Evaluation of 1,2,4-oxadiazolidinones: The Search for A Potential Non-β-lactam β-lactamase Inhibitors. (Masters Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/3578

Chicago Manual of Style (16th Edition):

Kalu, Chimdi Eke. “Synthesis and Evaluation of 1,2,4-oxadiazolidinones: The Search for A Potential Non-β-lactam β-lactamase Inhibitors.” 2019. Masters Thesis, East Tennessee State University. Accessed October 17, 2019. https://dc.etsu.edu/etd/3578.

MLA Handbook (7th Edition):

Kalu, Chimdi Eke. “Synthesis and Evaluation of 1,2,4-oxadiazolidinones: The Search for A Potential Non-β-lactam β-lactamase Inhibitors.” 2019. Web. 17 Oct 2019.

Vancouver:

Kalu CE. Synthesis and Evaluation of 1,2,4-oxadiazolidinones: The Search for A Potential Non-β-lactam β-lactamase Inhibitors. [Internet] [Masters thesis]. East Tennessee State University; 2019. [cited 2019 Oct 17]. Available from: https://dc.etsu.edu/etd/3578.

Council of Science Editors:

Kalu CE. Synthesis and Evaluation of 1,2,4-oxadiazolidinones: The Search for A Potential Non-β-lactam β-lactamase Inhibitors. [Masters Thesis]. East Tennessee State University; 2019. Available from: https://dc.etsu.edu/etd/3578

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