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You searched for subject:(cycloaddition). Showing records 1 – 30 of 150 total matches.

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1. Montagu, Aurélien. Préparation d'analoques de nucléosides et de leurs prodrogues pour une thérapie antivirale des poxvirus : Preparation of nucleoside analogues and their prodrugs targeting an antiviral therapy for poxviruses.

Degree: Docteur es, Chimie organique, 2011, Université d'Orléans

La menace bioterroriste que preprésente le virus de la variole et l’absence d’un traitement vaccinal ou curratif universel rend primordiale la mise au point d’un… (more)

Subjects/Keywords: Phosphononucléosides; Cycloaddition; Métathèse; Phosphononucléosides; Cycloaddition; Metathesis

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APA (6th Edition):

Montagu, A. (2011). Préparation d'analoques de nucléosides et de leurs prodrogues pour une thérapie antivirale des poxvirus : Preparation of nucleoside analogues and their prodrugs targeting an antiviral therapy for poxviruses. (Doctoral Dissertation). Université d'Orléans. Retrieved from http://www.theses.fr/2011ORLE2009

Chicago Manual of Style (16th Edition):

Montagu, Aurélien. “Préparation d'analoques de nucléosides et de leurs prodrogues pour une thérapie antivirale des poxvirus : Preparation of nucleoside analogues and their prodrugs targeting an antiviral therapy for poxviruses.” 2011. Doctoral Dissertation, Université d'Orléans. Accessed October 19, 2019. http://www.theses.fr/2011ORLE2009.

MLA Handbook (7th Edition):

Montagu, Aurélien. “Préparation d'analoques de nucléosides et de leurs prodrogues pour une thérapie antivirale des poxvirus : Preparation of nucleoside analogues and their prodrugs targeting an antiviral therapy for poxviruses.” 2011. Web. 19 Oct 2019.

Vancouver:

Montagu A. Préparation d'analoques de nucléosides et de leurs prodrogues pour une thérapie antivirale des poxvirus : Preparation of nucleoside analogues and their prodrugs targeting an antiviral therapy for poxviruses. [Internet] [Doctoral dissertation]. Université d'Orléans; 2011. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2011ORLE2009.

Council of Science Editors:

Montagu A. Préparation d'analoques de nucléosides et de leurs prodrogues pour une thérapie antivirale des poxvirus : Preparation of nucleoside analogues and their prodrugs targeting an antiviral therapy for poxviruses. [Doctoral Dissertation]. Université d'Orléans; 2011. Available from: http://www.theses.fr/2011ORLE2009


University of Alberta

2. Chan, Bryan Chi Kit. Cobalt(III)-Mediated Cycloalkenyl-Alkyne Cycloaddition and Cycloexpansion Reactions.

Degree: PhD, Department of Chemistry, 2010, University of Alberta

 A comprehensive investigation of cycloalkenyl-alkyne coupling reactions mediated by cobalt(III) templates is presented. The in situ derived cationic η3-cyclohexenyl complexes of cobalt(III) react with some… (more)

Subjects/Keywords: cycloexpansion; cycloalkenyl; cycloaddition

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APA (6th Edition):

Chan, B. C. K. (2010). Cobalt(III)-Mediated Cycloalkenyl-Alkyne Cycloaddition and Cycloexpansion Reactions. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/mw22v636t

Chicago Manual of Style (16th Edition):

Chan, Bryan Chi Kit. “Cobalt(III)-Mediated Cycloalkenyl-Alkyne Cycloaddition and Cycloexpansion Reactions.” 2010. Doctoral Dissertation, University of Alberta. Accessed October 19, 2019. https://era.library.ualberta.ca/files/mw22v636t.

MLA Handbook (7th Edition):

Chan, Bryan Chi Kit. “Cobalt(III)-Mediated Cycloalkenyl-Alkyne Cycloaddition and Cycloexpansion Reactions.” 2010. Web. 19 Oct 2019.

Vancouver:

Chan BCK. Cobalt(III)-Mediated Cycloalkenyl-Alkyne Cycloaddition and Cycloexpansion Reactions. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2019 Oct 19]. Available from: https://era.library.ualberta.ca/files/mw22v636t.

Council of Science Editors:

Chan BCK. Cobalt(III)-Mediated Cycloalkenyl-Alkyne Cycloaddition and Cycloexpansion Reactions. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/mw22v636t


University of Vermont

3. Draghici, Cristian. Discovery of a Novel Ring Fragmentation Reaction; Efficient Preparation of Tethered Aldehyde Ynoates and N-Containing Heterocycles;Radical Addition Approach to Asymmetric Amine Synthesis.

Degree: PhD, Chemistry, 2009, University of Vermont

 This dissertation describes the development of a novel ring fragmentation reaction in which cyclic γ-silyloxy-β-hydroxy-α-diazoesters undergo efficient rupture of the Cβ−Cγ bond when treated with… (more)

Subjects/Keywords: intramolecular dipolar cycloaddition; zaomethine ylides

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APA (6th Edition):

Draghici, C. (2009). Discovery of a Novel Ring Fragmentation Reaction; Efficient Preparation of Tethered Aldehyde Ynoates and N-Containing Heterocycles;Radical Addition Approach to Asymmetric Amine Synthesis. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/70

Chicago Manual of Style (16th Edition):

Draghici, Cristian. “Discovery of a Novel Ring Fragmentation Reaction; Efficient Preparation of Tethered Aldehyde Ynoates and N-Containing Heterocycles;Radical Addition Approach to Asymmetric Amine Synthesis.” 2009. Doctoral Dissertation, University of Vermont. Accessed October 19, 2019. https://scholarworks.uvm.edu/graddis/70.

MLA Handbook (7th Edition):

Draghici, Cristian. “Discovery of a Novel Ring Fragmentation Reaction; Efficient Preparation of Tethered Aldehyde Ynoates and N-Containing Heterocycles;Radical Addition Approach to Asymmetric Amine Synthesis.” 2009. Web. 19 Oct 2019.

Vancouver:

Draghici C. Discovery of a Novel Ring Fragmentation Reaction; Efficient Preparation of Tethered Aldehyde Ynoates and N-Containing Heterocycles;Radical Addition Approach to Asymmetric Amine Synthesis. [Internet] [Doctoral dissertation]. University of Vermont; 2009. [cited 2019 Oct 19]. Available from: https://scholarworks.uvm.edu/graddis/70.

Council of Science Editors:

Draghici C. Discovery of a Novel Ring Fragmentation Reaction; Efficient Preparation of Tethered Aldehyde Ynoates and N-Containing Heterocycles;Radical Addition Approach to Asymmetric Amine Synthesis. [Doctoral Dissertation]. University of Vermont; 2009. Available from: https://scholarworks.uvm.edu/graddis/70


University of Bradford

4. Abdullahi, Mohamed Hussain Haji. General method for the synthesis of pseudodisaccharides : Diels-Alder approach to the synthesis of pseudodisaccharides.

Degree: 2010, University of Bradford

 This thesis describes a new method for the synthesis of pseudodisaccharides containing a carbasugar analogue attached to a "true" sugar. The methodology is based on… (more)

Subjects/Keywords: 547.78; Pseudodisaccharides; Synthesis; Diels-Alder cycloaddition; Sugars; Cytotoxicity; Carbasugar; Cycloaddition

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APA (6th Edition):

Abdullahi, M. H. H. (2010). General method for the synthesis of pseudodisaccharides : Diels-Alder approach to the synthesis of pseudodisaccharides. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/4887

Chicago Manual of Style (16th Edition):

Abdullahi, Mohamed Hussain Haji. “General method for the synthesis of pseudodisaccharides : Diels-Alder approach to the synthesis of pseudodisaccharides.” 2010. Doctoral Dissertation, University of Bradford. Accessed October 19, 2019. http://hdl.handle.net/10454/4887.

MLA Handbook (7th Edition):

Abdullahi, Mohamed Hussain Haji. “General method for the synthesis of pseudodisaccharides : Diels-Alder approach to the synthesis of pseudodisaccharides.” 2010. Web. 19 Oct 2019.

Vancouver:

Abdullahi MHH. General method for the synthesis of pseudodisaccharides : Diels-Alder approach to the synthesis of pseudodisaccharides. [Internet] [Doctoral dissertation]. University of Bradford; 2010. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/10454/4887.

Council of Science Editors:

Abdullahi MHH. General method for the synthesis of pseudodisaccharides : Diels-Alder approach to the synthesis of pseudodisaccharides. [Doctoral Dissertation]. University of Bradford; 2010. Available from: http://hdl.handle.net/10454/4887


Université Paris-Sud – Paris XI

5. Laurent, Grégory. Réactions de cycloadditions énantiosélectives catalysées par des dérivés d’acides de Brønsted chiraux : Enantioselectives cycloadditions reactions catalyzed by chirals Brønsted acids derivatives.

Degree: Docteur es, Chimie, 2014, Université Paris-Sud – Paris XI

Ces travaux de thèse avaient pour objectif la synthèse asymétrique d’hétérocycles énantioenrichis par des méthodes à hautes valeurs ajoutées. Pour cela des catalyseurs ont été… (more)

Subjects/Keywords: Cycloaddition; Organocatalyse; Acide phosphorique; Énecarbamate; Cycloaddition; Organocatalysys; Phosphoric acid; Enecarbamate

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APA (6th Edition):

Laurent, G. (2014). Réactions de cycloadditions énantiosélectives catalysées par des dérivés d’acides de Brønsted chiraux : Enantioselectives cycloadditions reactions catalyzed by chirals Brønsted acids derivatives. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA112419

Chicago Manual of Style (16th Edition):

Laurent, Grégory. “Réactions de cycloadditions énantiosélectives catalysées par des dérivés d’acides de Brønsted chiraux : Enantioselectives cycloadditions reactions catalyzed by chirals Brønsted acids derivatives.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 19, 2019. http://www.theses.fr/2014PA112419.

MLA Handbook (7th Edition):

Laurent, Grégory. “Réactions de cycloadditions énantiosélectives catalysées par des dérivés d’acides de Brønsted chiraux : Enantioselectives cycloadditions reactions catalyzed by chirals Brønsted acids derivatives.” 2014. Web. 19 Oct 2019.

Vancouver:

Laurent G. Réactions de cycloadditions énantiosélectives catalysées par des dérivés d’acides de Brønsted chiraux : Enantioselectives cycloadditions reactions catalyzed by chirals Brønsted acids derivatives. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2014PA112419.

Council of Science Editors:

Laurent G. Réactions de cycloadditions énantiosélectives catalysées par des dérivés d’acides de Brønsted chiraux : Enantioselectives cycloadditions reactions catalyzed by chirals Brønsted acids derivatives. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA112419


University of Utah

6. Lane, Timothy Karl. The development of iron-catalyzed [2+2+2] cycloadditions to produce 6-membered nitrogen heterocycles.

Degree: PhD, Chemistry, 2015, University of Utah

 One of the greatest challenges in synthetic chemistry is the development of reactions that can efficiently afford target compounds without creating byproducts. One such class… (more)

Subjects/Keywords: Catalyst; Cycloaddition; Inorganic; Organometallic; Pyridine; Pyrimidine

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APA (6th Edition):

Lane, T. K. (2015). The development of iron-catalyzed [2+2+2] cycloadditions to produce 6-membered nitrogen heterocycles. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4058/rec/2441

Chicago Manual of Style (16th Edition):

Lane, Timothy Karl. “The development of iron-catalyzed [2+2+2] cycloadditions to produce 6-membered nitrogen heterocycles.” 2015. Doctoral Dissertation, University of Utah. Accessed October 19, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4058/rec/2441.

MLA Handbook (7th Edition):

Lane, Timothy Karl. “The development of iron-catalyzed [2+2+2] cycloadditions to produce 6-membered nitrogen heterocycles.” 2015. Web. 19 Oct 2019.

Vancouver:

Lane TK. The development of iron-catalyzed [2+2+2] cycloadditions to produce 6-membered nitrogen heterocycles. [Internet] [Doctoral dissertation]. University of Utah; 2015. [cited 2019 Oct 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4058/rec/2441.

Council of Science Editors:

Lane TK. The development of iron-catalyzed [2+2+2] cycloadditions to produce 6-membered nitrogen heterocycles. [Doctoral Dissertation]. University of Utah; 2015. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/4058/rec/2441


University of Cincinnati

7. Rodrigo, Sanjeewa K. Nickel Catalyzed Regioselective Reductive Coupling Reactions.

Degree: PhD, Arts and Sciences: Chemistry, 2014, University of Cincinnati

 Coupling or cycloaddition of two different p-components for the construction of more complex structural motifs is commonly used in organic synthesis. Most of these systems… (more)

Subjects/Keywords: Analytical Chemistry; Chemistry; reductive coupling reactions; cycloaddition

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APA (6th Edition):

Rodrigo, S. K. (2014). Nickel Catalyzed Regioselective Reductive Coupling Reactions. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622

Chicago Manual of Style (16th Edition):

Rodrigo, Sanjeewa K. “Nickel Catalyzed Regioselective Reductive Coupling Reactions.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed October 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622.

MLA Handbook (7th Edition):

Rodrigo, Sanjeewa K. “Nickel Catalyzed Regioselective Reductive Coupling Reactions.” 2014. Web. 19 Oct 2019.

Vancouver:

Rodrigo SK. Nickel Catalyzed Regioselective Reductive Coupling Reactions. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2019 Oct 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622.

Council of Science Editors:

Rodrigo SK. Nickel Catalyzed Regioselective Reductive Coupling Reactions. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1396532622


Miami University

8. Craft, Derek T. Palladium and Gold-Catalyzed transannular [4+3] cycloaddition reactions: Application to the ABCD carbon framework of Cortistatin A. A short synthesis of S-(+)-Siphonodiol. New chiral Au(I) N-heterocyclic carbene complexes and their use in intramolecular c.

Degree: PhD, Chemistry, 2010, Miami University

 Unit I, Using allene RCM reactions, 12, 14 and 16 membered furan/allene macrocycles were synthesized. Selective epoxidation reactions and Platinum catalysis were unable to initiate… (more)

Subjects/Keywords: Chemistry; transannular; cycloaddition; Cortistatin A; Gold

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APA (6th Edition):

Craft, D. T. (2010). Palladium and Gold-Catalyzed transannular [4+3] cycloaddition reactions: Application to the ABCD carbon framework of Cortistatin A. A short synthesis of S-(+)-Siphonodiol. New chiral Au(I) N-heterocyclic carbene complexes and their use in intramolecular c. (Doctoral Dissertation). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1272036117

Chicago Manual of Style (16th Edition):

Craft, Derek T. “Palladium and Gold-Catalyzed transannular [4+3] cycloaddition reactions: Application to the ABCD carbon framework of Cortistatin A. A short synthesis of S-(+)-Siphonodiol. New chiral Au(I) N-heterocyclic carbene complexes and their use in intramolecular c.” 2010. Doctoral Dissertation, Miami University. Accessed October 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=miami1272036117.

MLA Handbook (7th Edition):

Craft, Derek T. “Palladium and Gold-Catalyzed transannular [4+3] cycloaddition reactions: Application to the ABCD carbon framework of Cortistatin A. A short synthesis of S-(+)-Siphonodiol. New chiral Au(I) N-heterocyclic carbene complexes and their use in intramolecular c.” 2010. Web. 19 Oct 2019.

Vancouver:

Craft DT. Palladium and Gold-Catalyzed transannular [4+3] cycloaddition reactions: Application to the ABCD carbon framework of Cortistatin A. A short synthesis of S-(+)-Siphonodiol. New chiral Au(I) N-heterocyclic carbene complexes and their use in intramolecular c. [Internet] [Doctoral dissertation]. Miami University; 2010. [cited 2019 Oct 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1272036117.

Council of Science Editors:

Craft DT. Palladium and Gold-Catalyzed transannular [4+3] cycloaddition reactions: Application to the ABCD carbon framework of Cortistatin A. A short synthesis of S-(+)-Siphonodiol. New chiral Au(I) N-heterocyclic carbene complexes and their use in intramolecular c. [Doctoral Dissertation]. Miami University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1272036117

9. Vanbeselaere, Jorick. Analyses structurales et métaboliques de la sialylation des vertébrés : Structural and metabolic analysis in the sialylation of vertebrates.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2013, Université Lille I – Sciences et Technologies

Les travaux présentés explorent la diversité structurale des glycannes dans l’organisme modèle du Poisson Zèbre et analysent la régulation des sialoconjugués lors d’évènements physiopathologiques particuliers.… (more)

Subjects/Keywords: Glycome; Cycloaddition cuivre-azide-alcyne; 572.68

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APA (6th Edition):

Vanbeselaere, J. (2013). Analyses structurales et métaboliques de la sialylation des vertébrés : Structural and metabolic analysis in the sialylation of vertebrates. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2013LIL10153

Chicago Manual of Style (16th Edition):

Vanbeselaere, Jorick. “Analyses structurales et métaboliques de la sialylation des vertébrés : Structural and metabolic analysis in the sialylation of vertebrates.” 2013. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 19, 2019. http://www.theses.fr/2013LIL10153.

MLA Handbook (7th Edition):

Vanbeselaere, Jorick. “Analyses structurales et métaboliques de la sialylation des vertébrés : Structural and metabolic analysis in the sialylation of vertebrates.” 2013. Web. 19 Oct 2019.

Vancouver:

Vanbeselaere J. Analyses structurales et métaboliques de la sialylation des vertébrés : Structural and metabolic analysis in the sialylation of vertebrates. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2013. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2013LIL10153.

Council of Science Editors:

Vanbeselaere J. Analyses structurales et métaboliques de la sialylation des vertébrés : Structural and metabolic analysis in the sialylation of vertebrates. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2013. Available from: http://www.theses.fr/2013LIL10153


Wayne State University

10. Abou Aleiwi, Bilal. Transition Metal-Mediated Higher-Order Cycloaddition Reactions: Application To The Total Synthesis Of Complex Natural Products.

Degree: PhD, Chemistry, 2010, Wayne State University

  ABSTRACT TRANSITION METAL-MEDIATED HIGHER-ORDER CYCLOADDITION REACTIONS: APPLICATION TO THE TOTAL SYNTHESIS OF COMPLEX NATURAL PRODUCTS by BILAL ABOU ALEIWI October 2010 Advisor: Dr. James… (more)

Subjects/Keywords: HIGHER ORDER CYCLOADDITION REACTIONS; Organic Chemistry

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APA (6th Edition):

Abou Aleiwi, B. (2010). Transition Metal-Mediated Higher-Order Cycloaddition Reactions: Application To The Total Synthesis Of Complex Natural Products. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/136

Chicago Manual of Style (16th Edition):

Abou Aleiwi, Bilal. “Transition Metal-Mediated Higher-Order Cycloaddition Reactions: Application To The Total Synthesis Of Complex Natural Products.” 2010. Doctoral Dissertation, Wayne State University. Accessed October 19, 2019. https://digitalcommons.wayne.edu/oa_dissertations/136.

MLA Handbook (7th Edition):

Abou Aleiwi, Bilal. “Transition Metal-Mediated Higher-Order Cycloaddition Reactions: Application To The Total Synthesis Of Complex Natural Products.” 2010. Web. 19 Oct 2019.

Vancouver:

Abou Aleiwi B. Transition Metal-Mediated Higher-Order Cycloaddition Reactions: Application To The Total Synthesis Of Complex Natural Products. [Internet] [Doctoral dissertation]. Wayne State University; 2010. [cited 2019 Oct 19]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/136.

Council of Science Editors:

Abou Aleiwi B. Transition Metal-Mediated Higher-Order Cycloaddition Reactions: Application To The Total Synthesis Of Complex Natural Products. [Doctoral Dissertation]. Wayne State University; 2010. Available from: https://digitalcommons.wayne.edu/oa_dissertations/136


Boston College

11. Fort, Eric Henry. Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems.

Degree: PhD, Chemistry, 2010, Boston College

 The work described herein stems from an effort to develop a method for growing single-chirality carbon nanotubes from small hydrocarbon templates using a Diels-Alder cycloaddition/rearomatization… (more)

Subjects/Keywords: Armchair; Carbon Nanotubes; cycloaddition; Diels-Alder; rearomatization

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APA (6th Edition):

Fort, E. H. (2010). Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101647

Chicago Manual of Style (16th Edition):

Fort, Eric Henry. “Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems.” 2010. Doctoral Dissertation, Boston College. Accessed October 19, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101647.

MLA Handbook (7th Edition):

Fort, Eric Henry. “Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems.” 2010. Web. 19 Oct 2019.

Vancouver:

Fort EH. Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems. [Internet] [Doctoral dissertation]. Boston College; 2010. [cited 2019 Oct 19]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101647.

Council of Science Editors:

Fort EH. Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems. [Doctoral Dissertation]. Boston College; 2010. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101647


University of Notre Dame

12. Joshua Kyle Bolger. Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>.

Degree: PhD, Chemistry and Biochemistry, 2009, University of Notre Dame

  Acylnitroso cycloadducts have proven to be valuable intermediates in the syntheses of a plethora of biologically active molecules. The utility of relatively simple intermediates… (more)

Subjects/Keywords: acylnitroso cycloaddition; lipoxygenase inhibitors; regioselective ring-opening

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APA (6th Edition):

Bolger, J. K. (2009). Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/7p88cf97h8n

Chicago Manual of Style (16th Edition):

Bolger, Joshua Kyle. “Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>.” 2009. Doctoral Dissertation, University of Notre Dame. Accessed October 19, 2019. https://curate.nd.edu/show/7p88cf97h8n.

MLA Handbook (7th Edition):

Bolger, Joshua Kyle. “Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>.” 2009. Web. 19 Oct 2019.

Vancouver:

Bolger JK. Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2009. [cited 2019 Oct 19]. Available from: https://curate.nd.edu/show/7p88cf97h8n.

Council of Science Editors:

Bolger JK. Regioselective Copper-Mediated Organometallic Ring Openings of Acylnitroso Cycloadducts and the Development of 5-Lipoxygenase Inhibitors</h1>. [Doctoral Dissertation]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/7p88cf97h8n


University of Minnesota

13. 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 19, 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. 19 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 19]. 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


University of Bath

14. Moss, William Osburn. Novel amino acid synthons based on ketene thioacetals.

Degree: PhD, 1990, University of Bath

Subjects/Keywords: 547; Cycloaddition reactions

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APA (6th Edition):

Moss, W. O. (1990). Novel amino acid synthons based on ketene thioacetals. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/novel-amino-acid-synthons-based-on-ketene-thioacetals(eadd46cf-05cb-475a-851a-074ee84679ce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253997

Chicago Manual of Style (16th Edition):

Moss, William Osburn. “Novel amino acid synthons based on ketene thioacetals.” 1990. Doctoral Dissertation, University of Bath. Accessed October 19, 2019. https://researchportal.bath.ac.uk/en/studentthesis/novel-amino-acid-synthons-based-on-ketene-thioacetals(eadd46cf-05cb-475a-851a-074ee84679ce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253997.

MLA Handbook (7th Edition):

Moss, William Osburn. “Novel amino acid synthons based on ketene thioacetals.” 1990. Web. 19 Oct 2019.

Vancouver:

Moss WO. Novel amino acid synthons based on ketene thioacetals. [Internet] [Doctoral dissertation]. University of Bath; 1990. [cited 2019 Oct 19]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/novel-amino-acid-synthons-based-on-ketene-thioacetals(eadd46cf-05cb-475a-851a-074ee84679ce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253997.

Council of Science Editors:

Moss WO. Novel amino acid synthons based on ketene thioacetals. [Doctoral Dissertation]. University of Bath; 1990. Available from: https://researchportal.bath.ac.uk/en/studentthesis/novel-amino-acid-synthons-based-on-ketene-thioacetals(eadd46cf-05cb-475a-851a-074ee84679ce).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253997


Princeton University

15. Hoyt, Jordan. Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions .

Degree: PhD, 2015, Princeton University

 The synthesis of a new bis(imino)pyridine iron dinitogen compound, (iPr(tb)PDI)Fe(N2)2, was undertaken in order to explore the effect of restricting imine dissociation on catalysis. While… (more)

Subjects/Keywords: Catalysis; Cycloaddition; Cycloisomerization; Hydrogenation; Hydrosilylation; Iron

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APA (6th Edition):

Hoyt, J. (2015). Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp0112579v570

Chicago Manual of Style (16th Edition):

Hoyt, Jordan. “Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions .” 2015. Doctoral Dissertation, Princeton University. Accessed October 19, 2019. http://arks.princeton.edu/ark:/88435/dsp0112579v570.

MLA Handbook (7th Edition):

Hoyt, Jordan. “Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions .” 2015. Web. 19 Oct 2019.

Vancouver:

Hoyt J. Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions . [Internet] [Doctoral dissertation]. Princeton University; 2015. [cited 2019 Oct 19]. Available from: http://arks.princeton.edu/ark:/88435/dsp0112579v570.

Council of Science Editors:

Hoyt J. Iron Catalyzed C-X (X = C, Si, B, H) Bond Forming Reactions . [Doctoral Dissertation]. Princeton University; 2015. Available from: http://arks.princeton.edu/ark:/88435/dsp0112579v570


Johannes Gutenberg Universität Mainz

16. Nissen, Felix. Synthese von Carbolinen durch übergangsmetall-katalysierte [2+2+2]-Cycloaddition von Alkinen und Nitrilen: Ein neuer Weg zur Totalsynthese von Lavendamycin.

Degree: 2008, Johannes Gutenberg Universität Mainz

Carboline sind eine große Gruppe von natürlich vorkommenden Alkaloiden, die eine tricyclische Pyrido[b]indol-Ringstruktur gemeinsam habe. Das breite Spektrum biologischer Eigenschaften dieser Verbindungsklasse macht sie zu… (more)

Subjects/Keywords: Cycloaddition, Pyridin, Lavendamycin, Inamide, alkin; cycloaddition, pyridine, lavendamycin, ynamides, alkyne; Chemistry and allied sciences

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APA (6th Edition):

Nissen, F. (2008). Synthese von Carbolinen durch übergangsmetall-katalysierte [2+2+2]-Cycloaddition von Alkinen und Nitrilen: Ein neuer Weg zur Totalsynthese von Lavendamycin. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2011/2561/

Chicago Manual of Style (16th Edition):

Nissen, Felix. “Synthese von Carbolinen durch übergangsmetall-katalysierte [2+2+2]-Cycloaddition von Alkinen und Nitrilen: Ein neuer Weg zur Totalsynthese von Lavendamycin.” 2008. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed October 19, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2011/2561/.

MLA Handbook (7th Edition):

Nissen, Felix. “Synthese von Carbolinen durch übergangsmetall-katalysierte [2+2+2]-Cycloaddition von Alkinen und Nitrilen: Ein neuer Weg zur Totalsynthese von Lavendamycin.” 2008. Web. 19 Oct 2019.

Vancouver:

Nissen F. Synthese von Carbolinen durch übergangsmetall-katalysierte [2+2+2]-Cycloaddition von Alkinen und Nitrilen: Ein neuer Weg zur Totalsynthese von Lavendamycin. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2008. [cited 2019 Oct 19]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2011/2561/.

Council of Science Editors:

Nissen F. Synthese von Carbolinen durch übergangsmetall-katalysierte [2+2+2]-Cycloaddition von Alkinen und Nitrilen: Ein neuer Weg zur Totalsynthese von Lavendamycin. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2008. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2011/2561/


Johannes Gutenberg Universität Mainz

17. Dassonneville, Benjamin. Synthesis of carbolines and analogues via rhodhium-catalyzed [2+2+2] cycloaddition with alkynyl-ynamides : application to the total synthesis of alkaloids.

Degree: 2010, Johannes Gutenberg Universität Mainz

The main research theme of this dissertation is the synthesis of g- and b-carbolines using a metal-catalyzed [2+2+2] cycloaddition strategy of tethered alkynyl-ynamides (diynes) with… (more)

Subjects/Keywords: Carboline, Cycloaddition, Inamid, Rhodium; Carboline, Cycloaddition, Ynamide, Rhodium; Chemistry and allied sciences

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APA (6th Edition):

Dassonneville, B. (2010). Synthesis of carbolines and analogues via rhodhium-catalyzed [2+2+2] cycloaddition with alkynyl-ynamides : application to the total synthesis of alkaloids. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3404/

Chicago Manual of Style (16th Edition):

Dassonneville, Benjamin. “Synthesis of carbolines and analogues via rhodhium-catalyzed [2+2+2] cycloaddition with alkynyl-ynamides : application to the total synthesis of alkaloids.” 2010. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed October 19, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2013/3404/.

MLA Handbook (7th Edition):

Dassonneville, Benjamin. “Synthesis of carbolines and analogues via rhodhium-catalyzed [2+2+2] cycloaddition with alkynyl-ynamides : application to the total synthesis of alkaloids.” 2010. Web. 19 Oct 2019.

Vancouver:

Dassonneville B. Synthesis of carbolines and analogues via rhodhium-catalyzed [2+2+2] cycloaddition with alkynyl-ynamides : application to the total synthesis of alkaloids. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2010. [cited 2019 Oct 19]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3404/.

Council of Science Editors:

Dassonneville B. Synthesis of carbolines and analogues via rhodhium-catalyzed [2+2+2] cycloaddition with alkynyl-ynamides : application to the total synthesis of alkaloids. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2010. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3404/


McMaster University

18. Rambarran, Talena. New Routes to Functional Siloxanes: Applications of the Thermal Azide-Alkyne Cycloaddition for the Silicone Chemist.

Degree: PhD, 2016, McMaster University

Silicone oils (polysiloxane) and elastomers are a class of hydrophobic polymers with an extensive range of uses. While the high hydrophobicity can be beneficial in… (more)

Subjects/Keywords: silicones; azide-alkyne cycloaddition; click chemistry; modification; Huisgen 1,3 dipolar cycloaddition; thermal; PDMS

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APA (6th Edition):

Rambarran, T. (2016). New Routes to Functional Siloxanes: Applications of the Thermal Azide-Alkyne Cycloaddition for the Silicone Chemist. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/20557

Chicago Manual of Style (16th Edition):

Rambarran, Talena. “New Routes to Functional Siloxanes: Applications of the Thermal Azide-Alkyne Cycloaddition for the Silicone Chemist.” 2016. Doctoral Dissertation, McMaster University. Accessed October 19, 2019. http://hdl.handle.net/11375/20557.

MLA Handbook (7th Edition):

Rambarran, Talena. “New Routes to Functional Siloxanes: Applications of the Thermal Azide-Alkyne Cycloaddition for the Silicone Chemist.” 2016. Web. 19 Oct 2019.

Vancouver:

Rambarran T. New Routes to Functional Siloxanes: Applications of the Thermal Azide-Alkyne Cycloaddition for the Silicone Chemist. [Internet] [Doctoral dissertation]. McMaster University; 2016. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/11375/20557.

Council of Science Editors:

Rambarran T. New Routes to Functional Siloxanes: Applications of the Thermal Azide-Alkyne Cycloaddition for the Silicone Chemist. [Doctoral Dissertation]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20557

19. Plougastel, Lucie. Développement de la cycloaddition entre les sydnones et les alcynes tendus pour des applications en bioconjugaison : Development of the strain promoted sydnone-alkyne cycloaddition for bioconjugation applications.

Degree: Docteur es, Chimie, 2016, Paris Saclay

La découverte et l’exploration des réactions bio-orthogonales pour le marquage spécifique d’entités biologiques est un défi majeur à portée de main depuis une dizaine d’années.… (more)

Subjects/Keywords: Chimie click; Réactions bioorthogonales; Bioconjugaison; Cycloaddition; Sydnones; Click chemistry; Bio-Orthogonal reactions; Bioconjugation; Cycloaddition; Sydnones

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APA (6th Edition):

Plougastel, L. (2016). Développement de la cycloaddition entre les sydnones et les alcynes tendus pour des applications en bioconjugaison : Development of the strain promoted sydnone-alkyne cycloaddition for bioconjugation applications. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2016SACLS328

Chicago Manual of Style (16th Edition):

Plougastel, Lucie. “Développement de la cycloaddition entre les sydnones et les alcynes tendus pour des applications en bioconjugaison : Development of the strain promoted sydnone-alkyne cycloaddition for bioconjugation applications.” 2016. Doctoral Dissertation, Paris Saclay. Accessed October 19, 2019. http://www.theses.fr/2016SACLS328.

MLA Handbook (7th Edition):

Plougastel, Lucie. “Développement de la cycloaddition entre les sydnones et les alcynes tendus pour des applications en bioconjugaison : Development of the strain promoted sydnone-alkyne cycloaddition for bioconjugation applications.” 2016. Web. 19 Oct 2019.

Vancouver:

Plougastel L. Développement de la cycloaddition entre les sydnones et les alcynes tendus pour des applications en bioconjugaison : Development of the strain promoted sydnone-alkyne cycloaddition for bioconjugation applications. [Internet] [Doctoral dissertation]. Paris Saclay; 2016. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2016SACLS328.

Council of Science Editors:

Plougastel L. Développement de la cycloaddition entre les sydnones et les alcynes tendus pour des applications en bioconjugaison : Development of the strain promoted sydnone-alkyne cycloaddition for bioconjugation applications. [Doctoral Dissertation]. Paris Saclay; 2016. Available from: http://www.theses.fr/2016SACLS328

20. 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 19, 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. 19 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 19]. 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

21. 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 19, 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. 19 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 19]. 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

22. 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 19, 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. 19 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 19]. 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

23. Mandel, Jérémie. Approches synthétiques de tétrahydroisoquinoléines par cyclisation Pallado-Catalysée & synthèse de composés spirocétaliques par RRM : A Pallado-Catalyzed cycloaddition for a new acces to Tetrahydroisoquinolins & a ring rearrangement metathesis strategy for the rapid elaboration of Spiroketal.

Degree: Docteur es, Chimie organique, 2010, Mulhouse

Après avoir exposé les enjeux de ce travail en présentant dans le chapitre 1 les produits naturels possédant le motif tétrahydroisoquinoléinique, leurs intérêts pharmacologiques et… (more)

Subjects/Keywords: Tetrahydroisoquinoléine; Spirocétal; Métathèse; Palladium; Cycloaddition; Alpha-alcoxyfurane; Tetrahydroisoquinolin; Spiroketal; Metathesis; Palladium; Cycloaddition; Alpha-alcoxyfurane

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APA (6th Edition):

Mandel, J. (2010). Approches synthétiques de tétrahydroisoquinoléines par cyclisation Pallado-Catalysée & synthèse de composés spirocétaliques par RRM : A Pallado-Catalyzed cycloaddition for a new acces to Tetrahydroisoquinolins & a ring rearrangement metathesis strategy for the rapid elaboration of Spiroketal. (Doctoral Dissertation). Mulhouse. Retrieved from http://www.theses.fr/2010MULH3199

Chicago Manual of Style (16th Edition):

Mandel, Jérémie. “Approches synthétiques de tétrahydroisoquinoléines par cyclisation Pallado-Catalysée & synthèse de composés spirocétaliques par RRM : A Pallado-Catalyzed cycloaddition for a new acces to Tetrahydroisoquinolins & a ring rearrangement metathesis strategy for the rapid elaboration of Spiroketal.” 2010. Doctoral Dissertation, Mulhouse. Accessed October 19, 2019. http://www.theses.fr/2010MULH3199.

MLA Handbook (7th Edition):

Mandel, Jérémie. “Approches synthétiques de tétrahydroisoquinoléines par cyclisation Pallado-Catalysée & synthèse de composés spirocétaliques par RRM : A Pallado-Catalyzed cycloaddition for a new acces to Tetrahydroisoquinolins & a ring rearrangement metathesis strategy for the rapid elaboration of Spiroketal.” 2010. Web. 19 Oct 2019.

Vancouver:

Mandel J. Approches synthétiques de tétrahydroisoquinoléines par cyclisation Pallado-Catalysée & synthèse de composés spirocétaliques par RRM : A Pallado-Catalyzed cycloaddition for a new acces to Tetrahydroisoquinolins & a ring rearrangement metathesis strategy for the rapid elaboration of Spiroketal. [Internet] [Doctoral dissertation]. Mulhouse; 2010. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2010MULH3199.

Council of Science Editors:

Mandel J. Approches synthétiques de tétrahydroisoquinoléines par cyclisation Pallado-Catalysée & synthèse de composés spirocétaliques par RRM : A Pallado-Catalyzed cycloaddition for a new acces to Tetrahydroisoquinolins & a ring rearrangement metathesis strategy for the rapid elaboration of Spiroketal. [Doctoral Dissertation]. Mulhouse; 2010. Available from: http://www.theses.fr/2010MULH3199

24. Lacambra, Aitor. Nouvelle méthode pour des réactions de cycloaddition/désaromatisation stéreocontrolées sous conditions catalytiques : Novel methods for stereocontrolled cycloaddition/dearomatization reactions under catalytic conditions.

Degree: Docteur es, Chimie organique, 2017, Bordeaux

Les alcaloïdes sont, en général, une famille de composés hétérocycliquesd'origine végétale qui intègrent des atomes d'azote dans leur structure complexe.Leur intérêt réside dans les activités… (more)

Subjects/Keywords: Produit Naturels; Ferrocényle Prolines; Réactions de Cycloaddition; Natural Products; Ferrocenyl Prolines; Cycloaddition Reactions

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APA (6th Edition):

Lacambra, A. (2017). Nouvelle méthode pour des réactions de cycloaddition/désaromatisation stéreocontrolées sous conditions catalytiques : Novel methods for stereocontrolled cycloaddition/dearomatization reactions under catalytic conditions. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2017BORD0576

Chicago Manual of Style (16th Edition):

Lacambra, Aitor. “Nouvelle méthode pour des réactions de cycloaddition/désaromatisation stéreocontrolées sous conditions catalytiques : Novel methods for stereocontrolled cycloaddition/dearomatization reactions under catalytic conditions.” 2017. Doctoral Dissertation, Bordeaux. Accessed October 19, 2019. http://www.theses.fr/2017BORD0576.

MLA Handbook (7th Edition):

Lacambra, Aitor. “Nouvelle méthode pour des réactions de cycloaddition/désaromatisation stéreocontrolées sous conditions catalytiques : Novel methods for stereocontrolled cycloaddition/dearomatization reactions under catalytic conditions.” 2017. Web. 19 Oct 2019.

Vancouver:

Lacambra A. Nouvelle méthode pour des réactions de cycloaddition/désaromatisation stéreocontrolées sous conditions catalytiques : Novel methods for stereocontrolled cycloaddition/dearomatization reactions under catalytic conditions. [Internet] [Doctoral dissertation]. Bordeaux; 2017. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2017BORD0576.

Council of Science Editors:

Lacambra A. Nouvelle méthode pour des réactions de cycloaddition/désaromatisation stéreocontrolées sous conditions catalytiques : Novel methods for stereocontrolled cycloaddition/dearomatization reactions under catalytic conditions. [Doctoral Dissertation]. Bordeaux; 2017. Available from: http://www.theses.fr/2017BORD0576

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

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 19, 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. 19 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 19]. 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

26. Liu, Xiang. Nanomatériaux à base d'éléments de transition tardifs pour la catalyse de réactions "click" et impliquant des liaisons carbone-azote : Late transition-metal nanomaterials for the catalysis of “click” and other reactions involving C-N bond formation and reactivity.

Degree: Docteur es, Chimie, 2017, Rennes 1

La conception et la synthèse de nanomatériaux à base d'éléments de transition tardifs est d’un intérêt considérable pour des applications potentielles respectueuses de l’environnement en… (more)

Subjects/Keywords: Dendrimères; Nanoparticules; Cycloaddition; Complexes bases de Schiff; Catalyse; Dendrimers; Nanoparticles; Schiff-Base Complexes; Catalysis; Cycloaddition

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APA (6th Edition):

Liu, X. (2017). Nanomatériaux à base d'éléments de transition tardifs pour la catalyse de réactions "click" et impliquant des liaisons carbone-azote : Late transition-metal nanomaterials for the catalysis of “click” and other reactions involving C-N bond formation and reactivity. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2017REN1S113

Chicago Manual of Style (16th Edition):

Liu, Xiang. “Nanomatériaux à base d'éléments de transition tardifs pour la catalyse de réactions "click" et impliquant des liaisons carbone-azote : Late transition-metal nanomaterials for the catalysis of “click” and other reactions involving C-N bond formation and reactivity.” 2017. Doctoral Dissertation, Rennes 1. Accessed October 19, 2019. http://www.theses.fr/2017REN1S113.

MLA Handbook (7th Edition):

Liu, Xiang. “Nanomatériaux à base d'éléments de transition tardifs pour la catalyse de réactions "click" et impliquant des liaisons carbone-azote : Late transition-metal nanomaterials for the catalysis of “click” and other reactions involving C-N bond formation and reactivity.” 2017. Web. 19 Oct 2019.

Vancouver:

Liu X. Nanomatériaux à base d'éléments de transition tardifs pour la catalyse de réactions "click" et impliquant des liaisons carbone-azote : Late transition-metal nanomaterials for the catalysis of “click” and other reactions involving C-N bond formation and reactivity. [Internet] [Doctoral dissertation]. Rennes 1; 2017. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2017REN1S113.

Council of Science Editors:

Liu X. Nanomatériaux à base d'éléments de transition tardifs pour la catalyse de réactions "click" et impliquant des liaisons carbone-azote : Late transition-metal nanomaterials for the catalysis of “click” and other reactions involving C-N bond formation and reactivity. [Doctoral Dissertation]. Rennes 1; 2017. Available from: http://www.theses.fr/2017REN1S113

27. Duret, Guillaume. Synthèse de 4-aminopyridines par réaction de cycloaddition (4+2) d’ynamides : 4-aminopyridines synthesis through 4+2 cycloaddition of ynamides.

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

Les motifs de type pyridine sont des motifs centraux dans de nombreux domaines, aussi bien rencontrés dans divers principes actifs en chimie médicinale, qu’en agrochimie,… (more)

Subjects/Keywords: Pyridine; Cycloaddition 4+2; Flux; Micro-ondes; Ynamide; Furopyridine; Aminopyridine; Pyridine; 4+2 cycloaddition; Flux; Microvawes; Ynamide; Furopyridine; Aminopyridine; 547.2

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

APA (6th Edition):

Duret, G. (2017). Synthèse de 4-aminopyridines par réaction de cycloaddition (4+2) d’ynamides : 4-aminopyridines synthesis through 4+2 cycloaddition of ynamides. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAF012

Chicago Manual of Style (16th Edition):

Duret, Guillaume. “Synthèse de 4-aminopyridines par réaction de cycloaddition (4+2) d’ynamides : 4-aminopyridines synthesis through 4+2 cycloaddition of ynamides.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed October 19, 2019. http://www.theses.fr/2017STRAF012.

MLA Handbook (7th Edition):

Duret, Guillaume. “Synthèse de 4-aminopyridines par réaction de cycloaddition (4+2) d’ynamides : 4-aminopyridines synthesis through 4+2 cycloaddition of ynamides.” 2017. Web. 19 Oct 2019.

Vancouver:

Duret G. Synthèse de 4-aminopyridines par réaction de cycloaddition (4+2) d’ynamides : 4-aminopyridines synthesis through 4+2 cycloaddition of ynamides. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2017STRAF012.

Council of Science Editors:

Duret G. Synthèse de 4-aminopyridines par réaction de cycloaddition (4+2) d’ynamides : 4-aminopyridines synthesis through 4+2 cycloaddition of ynamides. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAF012


Université de Grenoble

28. Grisel, Julien. Des cyclobutanones chirales vers la (-)-Salinosporamide A : From chiral cylobutanones to (-)-Salinosporamide A.

Degree: Docteur es, Chimie, 2012, Université de Grenoble

Le travail présenté dans ce manuscrit concerne le développement d'une nouvelle voie d'accès à une famille de butyrolactames naturels à fort potentiel thérapeutique basé sur… (more)

Subjects/Keywords: Cycloaddition; Cétène symétrique; Cétène dissymétrique; Produits naturels; Lactame; Expansion de cycle; Cycloaddition; Symmetric ketene; Unsymmetric ketene; Natural products; Lactame; Cycle expansion

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

APA (6th Edition):

Grisel, J. (2012). Des cyclobutanones chirales vers la (-)-Salinosporamide A : From chiral cylobutanones to (-)-Salinosporamide A. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2012GRENV058

Chicago Manual of Style (16th Edition):

Grisel, Julien. “Des cyclobutanones chirales vers la (-)-Salinosporamide A : From chiral cylobutanones to (-)-Salinosporamide A.” 2012. Doctoral Dissertation, Université de Grenoble. Accessed October 19, 2019. http://www.theses.fr/2012GRENV058.

MLA Handbook (7th Edition):

Grisel, Julien. “Des cyclobutanones chirales vers la (-)-Salinosporamide A : From chiral cylobutanones to (-)-Salinosporamide A.” 2012. Web. 19 Oct 2019.

Vancouver:

Grisel J. Des cyclobutanones chirales vers la (-)-Salinosporamide A : From chiral cylobutanones to (-)-Salinosporamide A. [Internet] [Doctoral dissertation]. Université de Grenoble; 2012. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2012GRENV058.

Council of Science Editors:

Grisel J. Des cyclobutanones chirales vers la (-)-Salinosporamide A : From chiral cylobutanones to (-)-Salinosporamide A. [Doctoral Dissertation]. Université de Grenoble; 2012. Available from: http://www.theses.fr/2012GRENV058


Université de Grenoble

29. Rulliere, Pauline. Vers la synthèse totale de la (-)-salinosporamide A et de la (+)-lactacystine par cycloaddition [2+2] asymétrique : Towards the total synthesis of (-)-salinosporamide A and (+)-lactacystin based on asymmetric [2+2] cycloaddition.

Degree: Docteur es, Chimie organique, 2014, Université de Grenoble

Ce travail de thèse s'intéresse à la cycloaddition [2+2] asymétrique de cétènes et à son application en synthèse totale. La meilleure réactivité des oléfines Z… (more)

Subjects/Keywords: Synthèse totale; Cycloaddition [2+2]; Asymétrique; Salinosporamide A; Lactacystine; Cétène; Total synthesis; [2+2] cycloaddition; Asymmetric; Salinosporamide A; Lactacystin; Ketene; 540

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APA (6th Edition):

Rulliere, P. (2014). Vers la synthèse totale de la (-)-salinosporamide A et de la (+)-lactacystine par cycloaddition [2+2] asymétrique : Towards the total synthesis of (-)-salinosporamide A and (+)-lactacystin based on asymmetric [2+2] cycloaddition. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2014GRENV023

Chicago Manual of Style (16th Edition):

Rulliere, Pauline. “Vers la synthèse totale de la (-)-salinosporamide A et de la (+)-lactacystine par cycloaddition [2+2] asymétrique : Towards the total synthesis of (-)-salinosporamide A and (+)-lactacystin based on asymmetric [2+2] cycloaddition.” 2014. Doctoral Dissertation, Université de Grenoble. Accessed October 19, 2019. http://www.theses.fr/2014GRENV023.

MLA Handbook (7th Edition):

Rulliere, Pauline. “Vers la synthèse totale de la (-)-salinosporamide A et de la (+)-lactacystine par cycloaddition [2+2] asymétrique : Towards the total synthesis of (-)-salinosporamide A and (+)-lactacystin based on asymmetric [2+2] cycloaddition.” 2014. Web. 19 Oct 2019.

Vancouver:

Rulliere P. Vers la synthèse totale de la (-)-salinosporamide A et de la (+)-lactacystine par cycloaddition [2+2] asymétrique : Towards the total synthesis of (-)-salinosporamide A and (+)-lactacystin based on asymmetric [2+2] cycloaddition. [Internet] [Doctoral dissertation]. Université de Grenoble; 2014. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2014GRENV023.

Council of Science Editors:

Rulliere P. Vers la synthèse totale de la (-)-salinosporamide A et de la (+)-lactacystine par cycloaddition [2+2] asymétrique : Towards the total synthesis of (-)-salinosporamide A and (+)-lactacystin based on asymmetric [2+2] cycloaddition. [Doctoral Dissertation]. Université de Grenoble; 2014. Available from: http://www.theses.fr/2014GRENV023

30. Tillet, Guillaume. Utilisation de la réaction de cycloaddition de Huisgen afin d'améliorer les propriétés des polymères fluorés : Using Huisgen cycloaddition to improve fluorinated polymer properties.

Degree: Docteur es, Chimie et Physicochimie des matériaux, 2010, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier)

L'utilisation de la réaction de cycloaddition 1,3 de Huisgen afin d'optimiser les propriétés de polymères fluorés constitue l'objectif de ce travail. Cette cycloaddition a été… (more)

Subjects/Keywords: Réticulation; Cycloaddition de Huisgen; Click chemistry; Polymère fluoré; Photovoltaïque; Phthalocyanine; Crosslinking; Huisgen cycloaddition; Click chemistry; Fluorinated polymer; Photovoltaic; Phtalocyanine

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

APA (6th Edition):

Tillet, G. (2010). Utilisation de la réaction de cycloaddition de Huisgen afin d'améliorer les propriétés des polymères fluorés : Using Huisgen cycloaddition to improve fluorinated polymer properties. (Doctoral Dissertation). Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Retrieved from http://www.theses.fr/2010ENCM0011

Chicago Manual of Style (16th Edition):

Tillet, Guillaume. “Utilisation de la réaction de cycloaddition de Huisgen afin d'améliorer les propriétés des polymères fluorés : Using Huisgen cycloaddition to improve fluorinated polymer properties.” 2010. Doctoral Dissertation, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Accessed October 19, 2019. http://www.theses.fr/2010ENCM0011.

MLA Handbook (7th Edition):

Tillet, Guillaume. “Utilisation de la réaction de cycloaddition de Huisgen afin d'améliorer les propriétés des polymères fluorés : Using Huisgen cycloaddition to improve fluorinated polymer properties.” 2010. Web. 19 Oct 2019.

Vancouver:

Tillet G. Utilisation de la réaction de cycloaddition de Huisgen afin d'améliorer les propriétés des polymères fluorés : Using Huisgen cycloaddition to improve fluorinated polymer properties. [Internet] [Doctoral dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2010. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2010ENCM0011.

Council of Science Editors:

Tillet G. Utilisation de la réaction de cycloaddition de Huisgen afin d'améliorer les propriétés des polymères fluorés : Using Huisgen cycloaddition to improve fluorinated polymer properties. [Doctoral Dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2010. Available from: http://www.theses.fr/2010ENCM0011

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