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You searched for subject:(cycloaddition). Showing records 1 – 30 of 436 total matches.

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Oregon State University

1. Naffziger, Michael R. Aryl acetylene substituent effects : the synthesis and application of biaryls.

Degree: MS, Chemistry, 2010, Oregon State University

 The work described herein details the synthesis and application of biphenyls that probe the effects of hydrogen, Cl / Br, and methyl substituents on the… (more)

Subjects/Keywords: cycloaddition

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APA (6th Edition):

Naffziger, M. R. (2010). Aryl acetylene substituent effects : the synthesis and application of biaryls. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/19650

Chicago Manual of Style (16th Edition):

Naffziger, Michael R. “Aryl acetylene substituent effects : the synthesis and application of biaryls.” 2010. Masters Thesis, Oregon State University. Accessed April 17, 2021. http://hdl.handle.net/1957/19650.

MLA Handbook (7th Edition):

Naffziger, Michael R. “Aryl acetylene substituent effects : the synthesis and application of biaryls.” 2010. Web. 17 Apr 2021.

Vancouver:

Naffziger MR. Aryl acetylene substituent effects : the synthesis and application of biaryls. [Internet] [Masters thesis]. Oregon State University; 2010. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1957/19650.

Council of Science Editors:

Naffziger MR. Aryl acetylene substituent effects : the synthesis and application of biaryls. [Masters Thesis]. Oregon State University; 2010. Available from: http://hdl.handle.net/1957/19650

2. 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 April 17, 2021. 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. 17 Apr 2021.

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 2021 Apr 17]. 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

3. 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 April 17, 2021. 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. 17 Apr 2021.

Vancouver:

Chan BCK. Cobalt(III)-Mediated Cycloalkenyl-Alkyne Cycloaddition and Cycloexpansion Reactions. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2021 Apr 17]. 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


NSYSU

4. Huang, Chang-Gin. An Efficient Synthesis of γ-Substituted α,β-Unsaturated δ-Lactams. Formal Synthesis of (±)-Protoemetinol.

Degree: Master, Chemistry, 2002, NSYSU

γ-Substituted α,β-unsaturated δ-lactams was synthesized from α-sulfinyl acetamides in three steps. Formal synthesis of (±)-Protoemetinol was also reported. Advisors/Committee Members: Chou, C. H. (chair), Nein-Chen Chang (committee member), none (chair).

Subjects/Keywords: cycloaddition reaction

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APA (6th Edition):

Huang, C. (2002). An Efficient Synthesis of γ-Substituted α,β-Unsaturated δ-Lactams. Formal Synthesis of (±)-Protoemetinol. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618102-094444

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):

Huang, Chang-Gin. “An Efficient Synthesis of γ-Substituted α,β-Unsaturated δ-Lactams. Formal Synthesis of (±)-Protoemetinol.” 2002. Thesis, NSYSU. Accessed April 17, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618102-094444.

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

MLA Handbook (7th Edition):

Huang, Chang-Gin. “An Efficient Synthesis of γ-Substituted α,β-Unsaturated δ-Lactams. Formal Synthesis of (±)-Protoemetinol.” 2002. Web. 17 Apr 2021.

Vancouver:

Huang C. An Efficient Synthesis of γ-Substituted α,β-Unsaturated δ-Lactams. Formal Synthesis of (±)-Protoemetinol. [Internet] [Thesis]. NSYSU; 2002. [cited 2021 Apr 17]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618102-094444.

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

Council of Science Editors:

Huang C. An Efficient Synthesis of γ-Substituted α,β-Unsaturated δ-Lactams. Formal Synthesis of (±)-Protoemetinol. [Thesis]. NSYSU; 2002. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0618102-094444

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


Université du Québec à Montréal

5. Zaghdane, Helmi. Études synthétiques de la (-)-kopsine via un réarrangement d'Ireland-Claisen et une cycloaddition de Diels-Alder intramoléculaire.

Degree: 2008, Université du Québec à Montréal

 La (-)-kopsine appartient à la famille des alcaloïdes aspidofractinine. Isolée pour la première fois en 1890 par l'équipe du professeur Ber à partir de plantes… (more)

Subjects/Keywords: Alcaloïde; Cycloaddition; Kopsine; Synthèse chimique

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APA (6th Edition):

Zaghdane, H. (2008). Études synthétiques de la (-)-kopsine via un réarrangement d'Ireland-Claisen et une cycloaddition de Diels-Alder intramoléculaire. (Thesis). Université du Québec à Montréal. Retrieved from http://www.archipel.uqam.ca/1322/1/M10373.pdf

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):

Zaghdane, Helmi. “Études synthétiques de la (-)-kopsine via un réarrangement d'Ireland-Claisen et une cycloaddition de Diels-Alder intramoléculaire.” 2008. Thesis, Université du Québec à Montréal. Accessed April 17, 2021. http://www.archipel.uqam.ca/1322/1/M10373.pdf.

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

MLA Handbook (7th Edition):

Zaghdane, Helmi. “Études synthétiques de la (-)-kopsine via un réarrangement d'Ireland-Claisen et une cycloaddition de Diels-Alder intramoléculaire.” 2008. Web. 17 Apr 2021.

Vancouver:

Zaghdane H. Études synthétiques de la (-)-kopsine via un réarrangement d'Ireland-Claisen et une cycloaddition de Diels-Alder intramoléculaire. [Internet] [Thesis]. Université du Québec à Montréal; 2008. [cited 2021 Apr 17]. Available from: http://www.archipel.uqam.ca/1322/1/M10373.pdf.

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

Council of Science Editors:

Zaghdane H. Études synthétiques de la (-)-kopsine via un réarrangement d'Ireland-Claisen et une cycloaddition de Diels-Alder intramoléculaire. [Thesis]. Université du Québec à Montréal; 2008. Available from: http://www.archipel.uqam.ca/1322/1/M10373.pdf

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

6. Santosh L Gaonkar. Synthesis of biologically active heterocycles via cycloaddition reactions; -.

Degree: Chemistry, 2006, University of Mysore

The thesis describes the synthesis of 1,2-oxazines, fused ring oxazines, newlinetetrahydropyridazines, fused ring pyridazines via [4+2] cycloaddition reactions newlinewhile 1,3,4-oxadiazoles, 2-isoxazolines, fused ring imidazoles etc… (more)

Subjects/Keywords: Chemistry; cycloaddition reactions; heterocycles

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APA (6th Edition):

Gaonkar, S. L. (2006). Synthesis of biologically active heterocycles via cycloaddition reactions; -. (Thesis). University of Mysore. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/15929

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):

Gaonkar, Santosh L. “Synthesis of biologically active heterocycles via cycloaddition reactions; -.” 2006. Thesis, University of Mysore. Accessed April 17, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/15929.

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

MLA Handbook (7th Edition):

Gaonkar, Santosh L. “Synthesis of biologically active heterocycles via cycloaddition reactions; -.” 2006. Web. 17 Apr 2021.

Vancouver:

Gaonkar SL. Synthesis of biologically active heterocycles via cycloaddition reactions; -. [Internet] [Thesis]. University of Mysore; 2006. [cited 2021 Apr 17]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/15929.

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

Council of Science Editors:

Gaonkar SL. Synthesis of biologically active heterocycles via cycloaddition reactions; -. [Thesis]. University of Mysore; 2006. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/15929

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

7. Wagner, Bernd. Homogene Goldkatalyse zur Darstellung neuartiger heterocyclischer Spiroverbindungen.

Degree: 2016, Technische Universität Dortmund

 In recent years, a variety of new entries to interesting heterocylic compounds has been reported in the field of gold catalysis. On this occasion, it… (more)

Subjects/Keywords: Goldkatalyse; Spiroacetale; Alkine; Cycloaddition; 540

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APA (6th Edition):

Wagner, B. (2016). Homogene Goldkatalyse zur Darstellung neuartiger heterocyclischer Spiroverbindungen. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-17255

Chicago Manual of Style (16th Edition):

Wagner, Bernd. “Homogene Goldkatalyse zur Darstellung neuartiger heterocyclischer Spiroverbindungen.” 2016. Doctoral Dissertation, Technische Universität Dortmund. Accessed April 17, 2021. http://dx.doi.org/10.17877/DE290R-17255.

MLA Handbook (7th Edition):

Wagner, Bernd. “Homogene Goldkatalyse zur Darstellung neuartiger heterocyclischer Spiroverbindungen.” 2016. Web. 17 Apr 2021.

Vancouver:

Wagner B. Homogene Goldkatalyse zur Darstellung neuartiger heterocyclischer Spiroverbindungen. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2016. [cited 2021 Apr 17]. Available from: http://dx.doi.org/10.17877/DE290R-17255.

Council of Science Editors:

Wagner B. Homogene Goldkatalyse zur Darstellung neuartiger heterocyclischer Spiroverbindungen. [Doctoral Dissertation]. Technische Universität Dortmund; 2016. Available from: http://dx.doi.org/10.17877/DE290R-17255


University of Guelph

8. Haner, Jamie. Synthesis of Substituted Oxabenzonorbornadienes and their Reactions.

Degree: MS, Department of Chemistry, 2011, University of Guelph

 This thesis describes investigations on the topic of the versatile organic scaffold, 7-oxabenzonorbornadiene. The synthesis of 2-alkyl substituted furans via iron-catalyzed coupling of Grignard reagents… (more)

Subjects/Keywords: Oxabenzonorbornadiene; Cycloaddition; Organic Chemistry; Synthesis

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APA (6th Edition):

Haner, J. (2011). Synthesis of Substituted Oxabenzonorbornadienes and their Reactions. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/2958

Chicago Manual of Style (16th Edition):

Haner, Jamie. “Synthesis of Substituted Oxabenzonorbornadienes and their Reactions.” 2011. Masters Thesis, University of Guelph. Accessed April 17, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/2958.

MLA Handbook (7th Edition):

Haner, Jamie. “Synthesis of Substituted Oxabenzonorbornadienes and their Reactions.” 2011. Web. 17 Apr 2021.

Vancouver:

Haner J. Synthesis of Substituted Oxabenzonorbornadienes and their Reactions. [Internet] [Masters thesis]. University of Guelph; 2011. [cited 2021 Apr 17]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/2958.

Council of Science Editors:

Haner J. Synthesis of Substituted Oxabenzonorbornadienes and their Reactions. [Masters Thesis]. University of Guelph; 2011. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/2958

9. Rajotte, Isabelle. Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome.

Degree: M. Sc., Chimie, 2016, Université de Sherbrooke

 Des travaux précédents ont explorés la réactivité des aminocarbènes de chrome. Dans cet ouvrage, il sera question d’appliquer cette réactivité à la synthèse de la… (more)

Subjects/Keywords: Cylindrocarine; Aminocarbène; Cycloaddition; Chrome; Aspidosperma

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APA (6th Edition):

Rajotte, I. (2016). Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome. (Masters Thesis). Université de Sherbrooke. Retrieved from http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_8742.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/8742/3/Rajotte_Isabelle_MSc_2016.pdf

Chicago Manual of Style (16th Edition):

Rajotte, Isabelle. “Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome.” 2016. Masters Thesis, Université de Sherbrooke. Accessed April 17, 2021. http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_8742.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/8742/3/Rajotte_Isabelle_MSc_2016.pdf.

MLA Handbook (7th Edition):

Rajotte, Isabelle. “Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome.” 2016. Web. 17 Apr 2021.

Vancouver:

Rajotte I. Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome. [Internet] [Masters thesis]. Université de Sherbrooke; 2016. [cited 2021 Apr 17]. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_8742.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/8742/3/Rajotte_Isabelle_MSc_2016.pdf.

Council of Science Editors:

Rajotte I. Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome. [Masters Thesis]. Université de Sherbrooke; 2016. Available from: http://www.collectionscanada.gc.ca/obj/thesescanada/vol2/QSHERU/TC-QSHERU-11143_8742.pdf ; http://savoirs.usherbrooke.ca/bitstream/11143/8742/3/Rajotte_Isabelle_MSc_2016.pdf


University of Ottawa

10. Ranasinghe Gamage, Indeewari. New Reactivity Involving N-Isothiocyanates: Aminothiocarbonylation and [3+2] Cycloadditions to Form Molecules Containing NNCS Motifs .

Degree: 2017, University of Ottawa

 Nitrogen-containing heterocycles are of vital importance for the pharmaceutical and agrochemical industries. The Beauchemin group has been studying rare, amphoteric nitrogen-substituted isocyanates over the past… (more)

Subjects/Keywords: aminothiocarbonylation; heterocycles; cycloaddition; isothiocyanates

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APA (6th Edition):

Ranasinghe Gamage, I. (2017). New Reactivity Involving N-Isothiocyanates: Aminothiocarbonylation and [3+2] Cycloadditions to Form Molecules Containing NNCS Motifs . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/36042

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):

Ranasinghe Gamage, Indeewari. “New Reactivity Involving N-Isothiocyanates: Aminothiocarbonylation and [3+2] Cycloadditions to Form Molecules Containing NNCS Motifs .” 2017. Thesis, University of Ottawa. Accessed April 17, 2021. http://hdl.handle.net/10393/36042.

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

MLA Handbook (7th Edition):

Ranasinghe Gamage, Indeewari. “New Reactivity Involving N-Isothiocyanates: Aminothiocarbonylation and [3+2] Cycloadditions to Form Molecules Containing NNCS Motifs .” 2017. Web. 17 Apr 2021.

Vancouver:

Ranasinghe Gamage I. New Reactivity Involving N-Isothiocyanates: Aminothiocarbonylation and [3+2] Cycloadditions to Form Molecules Containing NNCS Motifs . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10393/36042.

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

Council of Science Editors:

Ranasinghe Gamage I. New Reactivity Involving N-Isothiocyanates: Aminothiocarbonylation and [3+2] Cycloadditions to Form Molecules Containing NNCS Motifs . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/36042

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


Université de Sherbrooke

11. Rajotte, Isabelle. Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome.

Degree: 2016, Université de Sherbrooke

 Des travaux précédents ont explorés la réactivité des aminocarbènes de chrome. Dans cet ouvrage, il sera question d’appliquer cette réactivité à la synthèse de la… (more)

Subjects/Keywords: Cylindrocarine; Aminocarbène; Cycloaddition; Chrome; Aspidosperma

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

APA (6th Edition):

Rajotte, I. (2016). Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/8742

Chicago Manual of Style (16th Edition):

Rajotte, Isabelle. “Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome.” 2016. Masters Thesis, Université de Sherbrooke. Accessed April 17, 2021. http://hdl.handle.net/11143/8742.

MLA Handbook (7th Edition):

Rajotte, Isabelle. “Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome.” 2016. Web. 17 Apr 2021.

Vancouver:

Rajotte I. Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome. [Internet] [Masters thesis]. Université de Sherbrooke; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11143/8742.

Council of Science Editors:

Rajotte I. Efforts vers la synthèse totale de la cylindrocarine par cycloaddition intramoléculaire impliquant des aminocarbènes de chrome. [Masters Thesis]. Université de Sherbrooke; 2016. Available from: http://hdl.handle.net/11143/8742

12. 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 April 17, 2021. 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 Apr 2021.

Vancouver:

LOCKETT-WALTERS B. The Tamura Cycloaddition: Mechanism and Enantiocontrol. [Internet] [Thesis]. Trinity College Dublin; 2019. [cited 2021 Apr 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 Minnesota

13. Jarvi, Melissa. Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition.

Degree: MS, Chemistry, 2019, University of Minnesota

 Isoxazole is a five membered heterocyclic compound containing oxygen and nitrogen atoms in the 1,2 positions. Isoxazole rings are found in natural products, such as… (more)

Subjects/Keywords: Cycloaddition; Hypervalent iodine(III); Isoxazole

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APA (6th Edition):

Jarvi, M. (2019). Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/208932

Chicago Manual of Style (16th Edition):

Jarvi, Melissa. “Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition.” 2019. Masters Thesis, University of Minnesota. Accessed April 17, 2021. http://hdl.handle.net/11299/208932.

MLA Handbook (7th Edition):

Jarvi, Melissa. “Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition.” 2019. Web. 17 Apr 2021.

Vancouver:

Jarvi M. Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition. [Internet] [Masters thesis]. University of Minnesota; 2019. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11299/208932.

Council of Science Editors:

Jarvi M. Regioselective Synthesis of Isoxazoles by Hypervalent Iodine(III) Reagent Mediated Oxidative Cycloaddition. [Masters Thesis]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/208932

14. Tsetan, Kunga. JULIA-KOCIENSKI APPROACH TO 4-SUBSTITUTED 1- ALKENYL-1H-1,2,3-TRIAZOLES.

Degree: MS(M.S.), Chemistry, 2016, City University of New York

  A modular approach to the synthesis of 4-substituted N-vinyltriazoles was developed. The triazole cores were assembled by copper-catalyzed 1,3-dipolar cycloaddition of 1-phenyl-1H-tetrazol-5-yl (PT) azidomethyl… (more)

Subjects/Keywords: triazole; cycloaddition; olefination; Chemistry

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APA (6th Edition):

Tsetan, K. (2016). JULIA-KOCIENSKI APPROACH TO 4-SUBSTITUTED 1- ALKENYL-1H-1,2,3-TRIAZOLES. (Thesis). City University of New York. Retrieved from https://academicworks.cuny.edu/cc_etds_theses/610

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):

Tsetan, Kunga. “JULIA-KOCIENSKI APPROACH TO 4-SUBSTITUTED 1- ALKENYL-1H-1,2,3-TRIAZOLES.” 2016. Thesis, City University of New York. Accessed April 17, 2021. https://academicworks.cuny.edu/cc_etds_theses/610.

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

MLA Handbook (7th Edition):

Tsetan, Kunga. “JULIA-KOCIENSKI APPROACH TO 4-SUBSTITUTED 1- ALKENYL-1H-1,2,3-TRIAZOLES.” 2016. Web. 17 Apr 2021.

Vancouver:

Tsetan K. JULIA-KOCIENSKI APPROACH TO 4-SUBSTITUTED 1- ALKENYL-1H-1,2,3-TRIAZOLES. [Internet] [Thesis]. City University of New York; 2016. [cited 2021 Apr 17]. Available from: https://academicworks.cuny.edu/cc_etds_theses/610.

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

Council of Science Editors:

Tsetan K. JULIA-KOCIENSKI APPROACH TO 4-SUBSTITUTED 1- ALKENYL-1H-1,2,3-TRIAZOLES. [Thesis]. City University of New York; 2016. Available from: https://academicworks.cuny.edu/cc_etds_theses/610

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


Brock University

15. Bissett, Tyler. Explorations of Intramolecular [5+2] Cycloadditions of Ring-Constrained Vinylcyclopropanes .

Degree: Department of Chemistry, 2014, Brock University

 The first example of a [5+2] cycloaddition reaction wherein the olefin of the vinylcyclopropyl moiety is constrained in a carbocycle was explored, and possible reasons… (more)

Subjects/Keywords: cycloaddition reaction; vinylcyclopropyl moiety

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APA (6th Edition):

Bissett, T. (2014). Explorations of Intramolecular [5+2] Cycloadditions of Ring-Constrained Vinylcyclopropanes . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/5741

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):

Bissett, Tyler. “Explorations of Intramolecular [5+2] Cycloadditions of Ring-Constrained Vinylcyclopropanes .” 2014. Thesis, Brock University. Accessed April 17, 2021. http://hdl.handle.net/10464/5741.

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

MLA Handbook (7th Edition):

Bissett, Tyler. “Explorations of Intramolecular [5+2] Cycloadditions of Ring-Constrained Vinylcyclopropanes .” 2014. Web. 17 Apr 2021.

Vancouver:

Bissett T. Explorations of Intramolecular [5+2] Cycloadditions of Ring-Constrained Vinylcyclopropanes . [Internet] [Thesis]. Brock University; 2014. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10464/5741.

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

Council of Science Editors:

Bissett T. Explorations of Intramolecular [5+2] Cycloadditions of Ring-Constrained Vinylcyclopropanes . [Thesis]. Brock University; 2014. Available from: http://hdl.handle.net/10464/5741

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


Université de Sherbrooke

16. D. Lefebvre, Louis-Philippe. Développement d'une réaction de cycloaddition (4+1) intramoléculaire formelle impliquant des aminocarbènes de chrome.

Degree: 2012, Université de Sherbrooke

 Ce mémoire résume les percées effectuées vers le développement d'une réaction de cycloaddition (4+1) intramoléculaire formelle entre des aminocarbènes de chrome et des diènes. Une… (more)

Subjects/Keywords: Cyclopentène; Cycloaddition; Diène; Fischer; Aminocarbène

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APA (6th Edition):

D. Lefebvre, L. (2012). Développement d'une réaction de cycloaddition (4+1) intramoléculaire formelle impliquant des aminocarbènes de chrome. (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/5752

Chicago Manual of Style (16th Edition):

D. Lefebvre, Louis-Philippe. “Développement d'une réaction de cycloaddition (4+1) intramoléculaire formelle impliquant des aminocarbènes de chrome.” 2012. Masters Thesis, Université de Sherbrooke. Accessed April 17, 2021. http://hdl.handle.net/11143/5752.

MLA Handbook (7th Edition):

D. Lefebvre, Louis-Philippe. “Développement d'une réaction de cycloaddition (4+1) intramoléculaire formelle impliquant des aminocarbènes de chrome.” 2012. Web. 17 Apr 2021.

Vancouver:

D. Lefebvre L. Développement d'une réaction de cycloaddition (4+1) intramoléculaire formelle impliquant des aminocarbènes de chrome. [Internet] [Masters thesis]. Université de Sherbrooke; 2012. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/11143/5752.

Council of Science Editors:

D. Lefebvre L. Développement d'une réaction de cycloaddition (4+1) intramoléculaire formelle impliquant des aminocarbènes de chrome. [Masters Thesis]. Université de Sherbrooke; 2012. Available from: http://hdl.handle.net/11143/5752


Université Paris-Sud – Paris XI

17. 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 April 17, 2021. 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. 17 Apr 2021.

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 2021 Apr 17]. 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 Guelph

18. Jack, Kelsey. Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes.

Degree: MS, Department of Chemistry, 2012, University of Guelph

 Oxabicyclic alkenes have been the focus of many synthetic studies as they are versatile compounds which act as synthetic intermediates to produce a variety of… (more)

Subjects/Keywords: Cycloaddition; Oxabicyclic Alkenes; Dimerization; Cycloaddition; Ring Opening; Ruthenium

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APA (6th Edition):

Jack, K. (2012). Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4738

Chicago Manual of Style (16th Edition):

Jack, Kelsey. “Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes.” 2012. Masters Thesis, University of Guelph. Accessed April 17, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4738.

MLA Handbook (7th Edition):

Jack, Kelsey. “Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes.” 2012. Web. 17 Apr 2021.

Vancouver:

Jack K. Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes. [Internet] [Masters thesis]. University of Guelph; 2012. [cited 2021 Apr 17]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4738.

Council of Science Editors:

Jack K. Investigations into the Ruthenium Catalyzed Ring Opening and Dimerization Reactions of Oxabicyclic Alkenes. [Masters Thesis]. University of Guelph; 2012. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4738


University of Utah

19. 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 April 17, 2021. 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. 17 Apr 2021.

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 2021 Apr 17]. 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


Université du Québec à Montréal

20. Desjardins, Marc-André. Cycloaddition 1,3-dipolaire intramoléculaire impliquant l'oxyde de nitrile et l'azoture comme dipôles et des 2-vinyloxazolidines dérivés de la noréphédrine.

Degree: 2008, Université du Québec à Montréal

 L'utilisation de la réaction de cycloaddition 1,3-dipolaire permet la formation d'hétérocycles hautement fonctionnalisés. L'étude de cette réaction de manière intramoléculaire permet la formation de centres… (more)

Subjects/Keywords: Phénylpropanolamine; Cycloaddition; Oxyde de nitrile; Isoxazoline

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APA (6th Edition):

Desjardins, M. (2008). Cycloaddition 1,3-dipolaire intramoléculaire impliquant l'oxyde de nitrile et l'azoture comme dipôles et des 2-vinyloxazolidines dérivés de la noréphédrine. (Thesis). Université du Québec à Montréal. Retrieved from http://www.archipel.uqam.ca/1047/1/M10355.pdf

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):

Desjardins, Marc-André. “Cycloaddition 1,3-dipolaire intramoléculaire impliquant l'oxyde de nitrile et l'azoture comme dipôles et des 2-vinyloxazolidines dérivés de la noréphédrine.” 2008. Thesis, Université du Québec à Montréal. Accessed April 17, 2021. http://www.archipel.uqam.ca/1047/1/M10355.pdf.

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

MLA Handbook (7th Edition):

Desjardins, Marc-André. “Cycloaddition 1,3-dipolaire intramoléculaire impliquant l'oxyde de nitrile et l'azoture comme dipôles et des 2-vinyloxazolidines dérivés de la noréphédrine.” 2008. Web. 17 Apr 2021.

Vancouver:

Desjardins M. Cycloaddition 1,3-dipolaire intramoléculaire impliquant l'oxyde de nitrile et l'azoture comme dipôles et des 2-vinyloxazolidines dérivés de la noréphédrine. [Internet] [Thesis]. Université du Québec à Montréal; 2008. [cited 2021 Apr 17]. Available from: http://www.archipel.uqam.ca/1047/1/M10355.pdf.

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

Council of Science Editors:

Desjardins M. Cycloaddition 1,3-dipolaire intramoléculaire impliquant l'oxyde de nitrile et l'azoture comme dipôles et des 2-vinyloxazolidines dérivés de la noréphédrine. [Thesis]. Université du Québec à Montréal; 2008. Available from: http://www.archipel.uqam.ca/1047/1/M10355.pdf

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


Texas A&M University

21. Wang, Xiaoshan. The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery.

Degree: PhD, Chemistry, 2018, Texas A&M University

 This study is composed of two parts. In the first part, we discussed nitrilimine-alkene cycloaddition for protein labeling. The mechanism of this nitrilimine-alkene cycloaddition was… (more)

Subjects/Keywords: nitrilimine-alkene cycloaddition; cyclic peptide; HDAC8 inhibitor

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APA (6th Edition):

Wang, X. (2018). The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173491

Chicago Manual of Style (16th Edition):

Wang, Xiaoshan. “The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery.” 2018. Doctoral Dissertation, Texas A&M University. Accessed April 17, 2021. http://hdl.handle.net/1969.1/173491.

MLA Handbook (7th Edition):

Wang, Xiaoshan. “The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery.” 2018. Web. 17 Apr 2021.

Vancouver:

Wang X. The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1969.1/173491.

Council of Science Editors:

Wang X. The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173491

22. Thomas, David Robert. Efforts towards understanding the nickel catalyzed cycloaddition of ciynes and nitriles to make pyridines.

Degree: MS, Chemistry, 2014, University of Utah

 Efforts towards understanding the nickel catalyzed cycloaddition of diynes and nitriles to make pyridines are described. During the course of this mechanistic study, a previously… (more)

Subjects/Keywords: Cycloaddition; Pyridine

…x5B;1a], kobs vs [IPr], and kobs vs [MeCN] for the cycloaddition of… …and angles in Figure 3. Dimer 3 was found to catalyze the cycloaddition of nitriles and… …x5D; for the cycloaddition of 4 at 0 °C in C7D8 10 Scheme 5. Possible mechanistic… …cycloaddition of nitriles and diynes to form pyridines. Kinetic studies showed a dependence of the… …28.8, 24.8, 23.7.19 Cycloaddition catalyzed by 3a. A stock solution of 3a was prepared by… 

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APA (6th Edition):

Thomas, D. R. (2014). Efforts towards understanding the nickel catalyzed cycloaddition of ciynes and nitriles to make pyridines. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2883/rec/842

Chicago Manual of Style (16th Edition):

Thomas, David Robert. “Efforts towards understanding the nickel catalyzed cycloaddition of ciynes and nitriles to make pyridines.” 2014. Masters Thesis, University of Utah. Accessed April 17, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2883/rec/842.

MLA Handbook (7th Edition):

Thomas, David Robert. “Efforts towards understanding the nickel catalyzed cycloaddition of ciynes and nitriles to make pyridines.” 2014. Web. 17 Apr 2021.

Vancouver:

Thomas DR. Efforts towards understanding the nickel catalyzed cycloaddition of ciynes and nitriles to make pyridines. [Internet] [Masters thesis]. University of Utah; 2014. [cited 2021 Apr 17]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2883/rec/842.

Council of Science Editors:

Thomas DR. Efforts towards understanding the nickel catalyzed cycloaddition of ciynes and nitriles to make pyridines. [Masters Thesis]. University of Utah; 2014. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2883/rec/842

23. 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 April 17, 2021. 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. 17 Apr 2021.

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 2021 Apr 17]. 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

24. Nöcker, Christina. Synthese von Naturstoff-basierten Substanzbibliotheken.

Degree: 2017, Technische Universität Dortmund

 The following thesis describes the synthesis of natural product inspired compound libraries. The synthesis of depsipeptides Chondramid C and analogues was conducted. The synthesis strategy… (more)

Subjects/Keywords: Cyclodepsipeptide; Sec14p; Cycloaddition; Organische Synthese; 570; 540

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APA (6th Edition):

Nöcker, C. (2017). Synthese von Naturstoff-basierten Substanzbibliotheken. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-17961

Chicago Manual of Style (16th Edition):

Nöcker, Christina. “Synthese von Naturstoff-basierten Substanzbibliotheken.” 2017. Doctoral Dissertation, Technische Universität Dortmund. Accessed April 17, 2021. http://dx.doi.org/10.17877/DE290R-17961.

MLA Handbook (7th Edition):

Nöcker, Christina. “Synthese von Naturstoff-basierten Substanzbibliotheken.” 2017. Web. 17 Apr 2021.

Vancouver:

Nöcker C. Synthese von Naturstoff-basierten Substanzbibliotheken. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2017. [cited 2021 Apr 17]. Available from: http://dx.doi.org/10.17877/DE290R-17961.

Council of Science Editors:

Nöcker C. Synthese von Naturstoff-basierten Substanzbibliotheken. [Doctoral Dissertation]. Technische Universität Dortmund; 2017. Available from: http://dx.doi.org/10.17877/DE290R-17961


Colorado State University

25. Dalton, Derek M. Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions.

Degree: PhD, Chemistry, 2013, Colorado State University

 Described herein are mechanistic studies and ligand development for Rh(I) catalyzed [2+2+2] cycloaddition reactions of alkene tethered isocyanates and exogenous alkynes. A mechanistic hypothesis has… (more)

Subjects/Keywords: cycloaddition; zinc; rhodium; enantioselective; heterocycles; catalysis

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APA (6th Edition):

Dalton, D. M. (2013). Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/80142

Chicago Manual of Style (16th Edition):

Dalton, Derek M. “Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions.” 2013. Doctoral Dissertation, Colorado State University. Accessed April 17, 2021. http://hdl.handle.net/10217/80142.

MLA Handbook (7th Edition):

Dalton, Derek M. “Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions.” 2013. Web. 17 Apr 2021.

Vancouver:

Dalton DM. Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions. [Internet] [Doctoral dissertation]. Colorado State University; 2013. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10217/80142.

Council of Science Editors:

Dalton DM. Mechanistic investigations and ligand development for rhodium catalyzed [2+2+2] and zinc catalyzed [4+2] cycloadditions. [Doctoral Dissertation]. Colorado State University; 2013. Available from: http://hdl.handle.net/10217/80142


University of Ottawa

26. 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 April 17, 2021. 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 Apr 2021.

Vancouver:

Rochon A. Cycloaddition Reactions of Ni(0) Difluorocarbene Complexes: Investigating the Formation of Various Perfluorometallacycles . [Internet] [Thesis]. University of Ottawa; 2019. [cited 2021 Apr 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


Boston College

27. 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 April 17, 2021. 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. 17 Apr 2021.

Vancouver:

Fort EH. Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems. [Internet] [Doctoral dissertation]. Boston College; 2010. [cited 2021 Apr 17]. 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 Bath

28. 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 April 17, 2021. 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. 17 Apr 2021.

Vancouver:

Moss WO. Novel amino acid synthons based on ketene thioacetals. [Internet] [Doctoral dissertation]. University of Bath; 1990. [cited 2021 Apr 17]. 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


University of Western Ontario

29. Farhadpour, Bahareh. Doubly Bonded Derivatives of Si and Ge: Cycloaddition Reactions and Polymer Chemistry.

Degree: 2017, University of Western Ontario

 (Di)tetrelenes are a fundamental class of unsaturated Group 14 compounds and play a central role in the synthesis of functional Group 14 compounds. The objective… (more)

Subjects/Keywords: Silene; Germene; Polygermene; Polysilene; Cycloaddition; Chemistry

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APA (6th Edition):

Farhadpour, B. (2017). Doubly Bonded Derivatives of Si and Ge: Cycloaddition Reactions and Polymer Chemistry. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4606

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):

Farhadpour, Bahareh. “Doubly Bonded Derivatives of Si and Ge: Cycloaddition Reactions and Polymer Chemistry.” 2017. Thesis, University of Western Ontario. Accessed April 17, 2021. https://ir.lib.uwo.ca/etd/4606.

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

MLA Handbook (7th Edition):

Farhadpour, Bahareh. “Doubly Bonded Derivatives of Si and Ge: Cycloaddition Reactions and Polymer Chemistry.” 2017. Web. 17 Apr 2021.

Vancouver:

Farhadpour B. Doubly Bonded Derivatives of Si and Ge: Cycloaddition Reactions and Polymer Chemistry. [Internet] [Thesis]. University of Western Ontario; 2017. [cited 2021 Apr 17]. Available from: https://ir.lib.uwo.ca/etd/4606.

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

Council of Science Editors:

Farhadpour B. Doubly Bonded Derivatives of Si and Ge: Cycloaddition Reactions and Polymer Chemistry. [Thesis]. University of Western Ontario; 2017. Available from: https://ir.lib.uwo.ca/etd/4606

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


University of Victoria

30. Morrow, Krista Maria Elena. Phosphorus-containing ruthenacycles: exploring their potential in processes relevant to hydrophosphination.

Degree: Dept. of Chemistry, 2012, University of Victoria

 Phosphorus-containing metallacycles formed from the [2+2] cycloaddition of unsaturated substrates at the Ru-P π-bond of [Ru(η5-indenyl)(PCy2)(PPh3)] (2) were examined as possible intermediates relevant to hydrophosphination.… (more)

Subjects/Keywords: cycloaddition; metallacycles; ruthenium; P ligands; hydrophosphination

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

APA (6th Edition):

Morrow, K. M. E. (2012). Phosphorus-containing ruthenacycles: exploring their potential in processes relevant to hydrophosphination. (Masters Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/3890

Chicago Manual of Style (16th Edition):

Morrow, Krista Maria Elena. “Phosphorus-containing ruthenacycles: exploring their potential in processes relevant to hydrophosphination.” 2012. Masters Thesis, University of Victoria. Accessed April 17, 2021. http://hdl.handle.net/1828/3890.

MLA Handbook (7th Edition):

Morrow, Krista Maria Elena. “Phosphorus-containing ruthenacycles: exploring their potential in processes relevant to hydrophosphination.” 2012. Web. 17 Apr 2021.

Vancouver:

Morrow KME. Phosphorus-containing ruthenacycles: exploring their potential in processes relevant to hydrophosphination. [Internet] [Masters thesis]. University of Victoria; 2012. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1828/3890.

Council of Science Editors:

Morrow KME. Phosphorus-containing ruthenacycles: exploring their potential in processes relevant to hydrophosphination. [Masters Thesis]. University of Victoria; 2012. Available from: http://hdl.handle.net/1828/3890

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