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You searched for subject:(Diels Alder reaction). Showing records 1 – 30 of 166 total matches.

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Oregon State University

1. Schwartz, Johanna Perkins. Expanding the scope of a Diels-Alder approach to biaryl synthesis.

Degree: PhD, Chemistry, 2009, Oregon State University

 A Diels-Alder approach to biaryls (DAB) has been applied towards the synthesis of highly substituted, programmable biaryl templates. Tri- and tetra-ortho-substituted biaryls can be produced… (more)

Subjects/Keywords: Biaryls; Diels-Alder reaction

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APA (6th Edition):

Schwartz, J. P. (2009). Expanding the scope of a Diels-Alder approach to biaryl synthesis. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/12403

Chicago Manual of Style (16th Edition):

Schwartz, Johanna Perkins. “Expanding the scope of a Diels-Alder approach to biaryl synthesis.” 2009. Doctoral Dissertation, Oregon State University. Accessed October 30, 2020. http://hdl.handle.net/1957/12403.

MLA Handbook (7th Edition):

Schwartz, Johanna Perkins. “Expanding the scope of a Diels-Alder approach to biaryl synthesis.” 2009. Web. 30 Oct 2020.

Vancouver:

Schwartz JP. Expanding the scope of a Diels-Alder approach to biaryl synthesis. [Internet] [Doctoral dissertation]. Oregon State University; 2009. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1957/12403.

Council of Science Editors:

Schwartz JP. Expanding the scope of a Diels-Alder approach to biaryl synthesis. [Doctoral Dissertation]. Oregon State University; 2009. Available from: http://hdl.handle.net/1957/12403

2. Barbosa, Jader da Silva. Estudo sobre a síntese de furanoliangolidos pela Reação de Diels-Alder.

Degree: Mestrado, Química, 2010, University of São Paulo

Nosso grupo de pesquisa já vem há alguns anos estudando métodos para a síntese do núcleo estrutural dos furanoeliangolidos, mais especificamente do goiazensolido. A estrutura… (more)

Subjects/Keywords: Diels-Alder reaction; Furanoheliangolides; furanoliangolidos; Reação de Diels-Alder

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APA (6th Edition):

Barbosa, J. d. S. (2010). Estudo sobre a síntese de furanoliangolidos pela Reação de Diels-Alder. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/59/59138/tde-08062010-185911/ ;

Chicago Manual of Style (16th Edition):

Barbosa, Jader da Silva. “Estudo sobre a síntese de furanoliangolidos pela Reação de Diels-Alder.” 2010. Masters Thesis, University of São Paulo. Accessed October 30, 2020. http://www.teses.usp.br/teses/disponiveis/59/59138/tde-08062010-185911/ ;.

MLA Handbook (7th Edition):

Barbosa, Jader da Silva. “Estudo sobre a síntese de furanoliangolidos pela Reação de Diels-Alder.” 2010. Web. 30 Oct 2020.

Vancouver:

Barbosa JdS. Estudo sobre a síntese de furanoliangolidos pela Reação de Diels-Alder. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2020 Oct 30]. Available from: http://www.teses.usp.br/teses/disponiveis/59/59138/tde-08062010-185911/ ;.

Council of Science Editors:

Barbosa JdS. Estudo sobre a síntese de furanoliangolidos pela Reação de Diels-Alder. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/59/59138/tde-08062010-185911/ ;


Oregon State University

3. Dei Rossi, Dale Raymond. The use of the Diels-Alder reaction in asymmetric synthesis.

Degree: MS, Chemistry, 1978, Oregon State University

 The Diels-Alder reaction represents a promising tool for use in asymmetric synthesis. The reaction involves a rigid transition state that facilitates the formation of one… (more)

Subjects/Keywords: Diels-Alder reaction

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APA (6th Edition):

Dei Rossi, D. R. (1978). The use of the Diels-Alder reaction in asymmetric synthesis. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/43388

Chicago Manual of Style (16th Edition):

Dei Rossi, Dale Raymond. “The use of the Diels-Alder reaction in asymmetric synthesis.” 1978. Masters Thesis, Oregon State University. Accessed October 30, 2020. http://hdl.handle.net/1957/43388.

MLA Handbook (7th Edition):

Dei Rossi, Dale Raymond. “The use of the Diels-Alder reaction in asymmetric synthesis.” 1978. Web. 30 Oct 2020.

Vancouver:

Dei Rossi DR. The use of the Diels-Alder reaction in asymmetric synthesis. [Internet] [Masters thesis]. Oregon State University; 1978. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1957/43388.

Council of Science Editors:

Dei Rossi DR. The use of the Diels-Alder reaction in asymmetric synthesis. [Masters Thesis]. Oregon State University; 1978. Available from: http://hdl.handle.net/1957/43388


Drexel University

4. Peterson, Amy Michelle. Development of remendable polymer composites using a thermoreversible reaction.

Degree: 2011, Drexel University

Materials that can repair cracks and recover from mechanical failure are desirable. Because remendable materials both repair and prevent the propagation of cracks on the… (more)

Subjects/Keywords: Chemical engineering; Composite materials; Diels-Alder reaction

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APA (6th Edition):

Peterson, A. M. (2011). Development of remendable polymer composites using a thermoreversible reaction. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/3534

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):

Peterson, Amy Michelle. “Development of remendable polymer composites using a thermoreversible reaction.” 2011. Thesis, Drexel University. Accessed October 30, 2020. http://hdl.handle.net/1860/3534.

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

MLA Handbook (7th Edition):

Peterson, Amy Michelle. “Development of remendable polymer composites using a thermoreversible reaction.” 2011. Web. 30 Oct 2020.

Vancouver:

Peterson AM. Development of remendable polymer composites using a thermoreversible reaction. [Internet] [Thesis]. Drexel University; 2011. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1860/3534.

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

Council of Science Editors:

Peterson AM. Development of remendable polymer composites using a thermoreversible reaction. [Thesis]. Drexel University; 2011. Available from: http://hdl.handle.net/1860/3534

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


University of Victoria

5. Clouston, Laurel L. The design and synthesis of C₃ symmetric ligands for lanthanide Lewis acid catalysis of the inverse demand hetero Diels-Alder reaction.

Degree: Department of Chemistry, 2017, University of Victoria

 The inverse demand hetero Diels-Alder reaction has been shown to be catalysed by commercially available, air-sensitive lanthanide Lewis acid catalysts such as Yb(fod)₃ . To… (more)

Subjects/Keywords: Lewis acids; Ligands; Diels-Alder reaction

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APA (6th Edition):

Clouston, L. L. (2017). The design and synthesis of C₃ symmetric ligands for lanthanide Lewis acid catalysis of the inverse demand hetero Diels-Alder reaction. (Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/8721

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):

Clouston, Laurel L. “The design and synthesis of C₃ symmetric ligands for lanthanide Lewis acid catalysis of the inverse demand hetero Diels-Alder reaction.” 2017. Thesis, University of Victoria. Accessed October 30, 2020. https://dspace.library.uvic.ca//handle/1828/8721.

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

MLA Handbook (7th Edition):

Clouston, Laurel L. “The design and synthesis of C₃ symmetric ligands for lanthanide Lewis acid catalysis of the inverse demand hetero Diels-Alder reaction.” 2017. Web. 30 Oct 2020.

Vancouver:

Clouston LL. The design and synthesis of C₃ symmetric ligands for lanthanide Lewis acid catalysis of the inverse demand hetero Diels-Alder reaction. [Internet] [Thesis]. University of Victoria; 2017. [cited 2020 Oct 30]. Available from: https://dspace.library.uvic.ca//handle/1828/8721.

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

Council of Science Editors:

Clouston LL. The design and synthesis of C₃ symmetric ligands for lanthanide Lewis acid catalysis of the inverse demand hetero Diels-Alder reaction. [Thesis]. University of Victoria; 2017. Available from: https://dspace.library.uvic.ca//handle/1828/8721

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


Montana State University

6. Boloor, Amogh G. Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol.

Degree: MS, College of Letters & Science, 1998, Montana State University

Subjects/Keywords: Diels-Alder reaction.

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APA (6th Edition):

Boloor, A. G. (1998). Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol. (Masters Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/8541

Chicago Manual of Style (16th Edition):

Boloor, Amogh G. “Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol.” 1998. Masters Thesis, Montana State University. Accessed October 30, 2020. https://scholarworks.montana.edu/xmlui/handle/1/8541.

MLA Handbook (7th Edition):

Boloor, Amogh G. “Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol.” 1998. Web. 30 Oct 2020.

Vancouver:

Boloor AG. Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol. [Internet] [Masters thesis]. Montana State University; 1998. [cited 2020 Oct 30]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/8541.

Council of Science Editors:

Boloor AG. Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol. [Masters Thesis]. Montana State University; 1998. Available from: https://scholarworks.montana.edu/xmlui/handle/1/8541

7. Eberlin, Ludovic. Novel applications of polyfunctionalised organoboron and nitroso compounds : Composés organoborylés polyfonctionnalisés et dérivés nitroso : nouvelles applications.

Degree: Docteur es, Chimie, 2016, Rennes 1; University of Durham

Cette thèse présente la réactivité de diènes polyfonctionnalisés incorporant un atome de bore (diènes borylés) en présence de composés de type nitroso. La première partie… (more)

Subjects/Keywords: Bore; Nitroso; Diels-Alder; Ene-Reaction; Multicomposants; Boron; Nitroso; Diels-Alder; Ene-Reaction; Multicomponents

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APA (6th Edition):

Eberlin, L. (2016). Novel applications of polyfunctionalised organoboron and nitroso compounds : Composés organoborylés polyfonctionnalisés et dérivés nitroso : nouvelles applications. (Doctoral Dissertation). Rennes 1; University of Durham. Retrieved from http://www.theses.fr/2016REN1S078

Chicago Manual of Style (16th Edition):

Eberlin, Ludovic. “Novel applications of polyfunctionalised organoboron and nitroso compounds : Composés organoborylés polyfonctionnalisés et dérivés nitroso : nouvelles applications.” 2016. Doctoral Dissertation, Rennes 1; University of Durham. Accessed October 30, 2020. http://www.theses.fr/2016REN1S078.

MLA Handbook (7th Edition):

Eberlin, Ludovic. “Novel applications of polyfunctionalised organoboron and nitroso compounds : Composés organoborylés polyfonctionnalisés et dérivés nitroso : nouvelles applications.” 2016. Web. 30 Oct 2020.

Vancouver:

Eberlin L. Novel applications of polyfunctionalised organoboron and nitroso compounds : Composés organoborylés polyfonctionnalisés et dérivés nitroso : nouvelles applications. [Internet] [Doctoral dissertation]. Rennes 1; University of Durham; 2016. [cited 2020 Oct 30]. Available from: http://www.theses.fr/2016REN1S078.

Council of Science Editors:

Eberlin L. Novel applications of polyfunctionalised organoboron and nitroso compounds : Composés organoborylés polyfonctionnalisés et dérivés nitroso : nouvelles applications. [Doctoral Dissertation]. Rennes 1; University of Durham; 2016. Available from: http://www.theses.fr/2016REN1S078

8. Bares, Hugo. Fonctionnalisation chimique du graphène, : vers des matériaux bidimentionnels photo actifs pour la reconnaissance et l'électronique moléculaire : Chemical functionalization of graphene.

Degree: Docteur es, Chimie organique, 2015, Bordeaux

Depuis la découverte des propriétés physiques et électroniques du graphène, un très grand nombre de méthodes visant à produire et modifier chimiquement le graphène ont… (more)

Subjects/Keywords: Graphène; Exfoliation en phase liquide; Fonctionnalisation du graphène; Reaction de Diels-Alder; Graphene; Liquid-phase exfoliation; Graphene functionalization; Diels-Alder reaction

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APA (6th Edition):

Bares, H. (2015). Fonctionnalisation chimique du graphène, : vers des matériaux bidimentionnels photo actifs pour la reconnaissance et l'électronique moléculaire : Chemical functionalization of graphene. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2015BORD0400

Chicago Manual of Style (16th Edition):

Bares, Hugo. “Fonctionnalisation chimique du graphène, : vers des matériaux bidimentionnels photo actifs pour la reconnaissance et l'électronique moléculaire : Chemical functionalization of graphene.” 2015. Doctoral Dissertation, Bordeaux. Accessed October 30, 2020. http://www.theses.fr/2015BORD0400.

MLA Handbook (7th Edition):

Bares, Hugo. “Fonctionnalisation chimique du graphène, : vers des matériaux bidimentionnels photo actifs pour la reconnaissance et l'électronique moléculaire : Chemical functionalization of graphene.” 2015. Web. 30 Oct 2020.

Vancouver:

Bares H. Fonctionnalisation chimique du graphène, : vers des matériaux bidimentionnels photo actifs pour la reconnaissance et l'électronique moléculaire : Chemical functionalization of graphene. [Internet] [Doctoral dissertation]. Bordeaux; 2015. [cited 2020 Oct 30]. Available from: http://www.theses.fr/2015BORD0400.

Council of Science Editors:

Bares H. Fonctionnalisation chimique du graphène, : vers des matériaux bidimentionnels photo actifs pour la reconnaissance et l'électronique moléculaire : Chemical functionalization of graphene. [Doctoral Dissertation]. Bordeaux; 2015. Available from: http://www.theses.fr/2015BORD0400

9. Qu, Yangyang. Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives.

Degree: Docteur es, Chimie, 2018, Université Paris-Saclay (ComUE)

Cette thèse porte sur la conception, la synthèse et la caractérisation de nouveaux dérivés accepteurs d'électrons. Elle se concentre sur l’étude des dérivés de la… (more)

Subjects/Keywords: Tétrazine; Benzonitrile; Thiatriazole; Fluorescence retardée; Réaction de couplage; Réaction Diels–Alder; Tetrazine; Benzonitrile; Thiatriazole; Delayed fluorescence; Coupling reaction; Diels–Alder reaction

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APA (6th Edition):

Qu, Y. (2018). Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2018SACLN051

Chicago Manual of Style (16th Edition):

Qu, Yangyang. “Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed October 30, 2020. http://www.theses.fr/2018SACLN051.

MLA Handbook (7th Edition):

Qu, Yangyang. “Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives.” 2018. Web. 30 Oct 2020.

Vancouver:

Qu Y. Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2020 Oct 30]. Available from: http://www.theses.fr/2018SACLN051.

Council of Science Editors:

Qu Y. Design, synthèse et caractérisation de dérivés aromatiques et hétérocycliques électrodéficitaires : Design, synthesis and characterization of electron-acceptor aromatic and heterocyclic derivatives. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLN051

10. Dantas de Araújo, Aline. Diels-Alder ligation of peptides and proteins.

Degree: 2005, Technische Universität Dortmund

 In light of the emerging area of protein chemistry, we demonstrated that the Diels-Alder ligation offers an advantageous new way for the site-selective functionalization and… (more)

Subjects/Keywords: Diels-Alder reaction; peptide ligation; protein modification; 540

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APA (6th Edition):

Dantas de Araújo, A. (2005). Diels-Alder ligation of peptides and proteins. (Thesis). Technische Universität Dortmund. Retrieved from http://hdl.handle.net/2003/20230

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):

Dantas de Araújo, Aline. “Diels-Alder ligation of peptides and proteins.” 2005. Thesis, Technische Universität Dortmund. Accessed October 30, 2020. http://hdl.handle.net/2003/20230.

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

MLA Handbook (7th Edition):

Dantas de Araújo, Aline. “Diels-Alder ligation of peptides and proteins.” 2005. Web. 30 Oct 2020.

Vancouver:

Dantas de Araújo A. Diels-Alder ligation of peptides and proteins. [Internet] [Thesis]. Technische Universität Dortmund; 2005. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2003/20230.

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

Council of Science Editors:

Dantas de Araújo A. Diels-Alder ligation of peptides and proteins. [Thesis]. Technische Universität Dortmund; 2005. Available from: http://hdl.handle.net/2003/20230

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


University of Alberta

11. Chew, Sew Yeu. Facial selective Diels-Alder reactions of (1R, 5R)-(+)-3-carbomethoxy-6,6-dimethylbicyclo-[3.1.1] hept-3-en-2-one. application to sesquiterpenoids synthesis.

Degree: PhD, Department of Chemistry, 1991, University of Alberta

Subjects/Keywords: Sesquiterpenes.; Diels-Alder reaction.

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APA (6th Edition):

Chew, S. Y. (1991). Facial selective Diels-Alder reactions of (1R, 5R)-(+)-3-carbomethoxy-6,6-dimethylbicyclo-[3.1.1] hept-3-en-2-one. application to sesquiterpenoids synthesis. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/dz010s39f

Chicago Manual of Style (16th Edition):

Chew, Sew Yeu. “Facial selective Diels-Alder reactions of (1R, 5R)-(+)-3-carbomethoxy-6,6-dimethylbicyclo-[3.1.1] hept-3-en-2-one. application to sesquiterpenoids synthesis.” 1991. Doctoral Dissertation, University of Alberta. Accessed October 30, 2020. https://era.library.ualberta.ca/files/dz010s39f.

MLA Handbook (7th Edition):

Chew, Sew Yeu. “Facial selective Diels-Alder reactions of (1R, 5R)-(+)-3-carbomethoxy-6,6-dimethylbicyclo-[3.1.1] hept-3-en-2-one. application to sesquiterpenoids synthesis.” 1991. Web. 30 Oct 2020.

Vancouver:

Chew SY. Facial selective Diels-Alder reactions of (1R, 5R)-(+)-3-carbomethoxy-6,6-dimethylbicyclo-[3.1.1] hept-3-en-2-one. application to sesquiterpenoids synthesis. [Internet] [Doctoral dissertation]. University of Alberta; 1991. [cited 2020 Oct 30]. Available from: https://era.library.ualberta.ca/files/dz010s39f.

Council of Science Editors:

Chew SY. Facial selective Diels-Alder reactions of (1R, 5R)-(+)-3-carbomethoxy-6,6-dimethylbicyclo-[3.1.1] hept-3-en-2-one. application to sesquiterpenoids synthesis. [Doctoral Dissertation]. University of Alberta; 1991. Available from: https://era.library.ualberta.ca/files/dz010s39f


University of Alberta

12. Han, Yongxin. S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones.

Degree: PhD, Department of Chemistry, 1992, University of Alberta

Subjects/Keywords: Diels-Alder reaction.; Chemical reactions.

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APA (6th Edition):

Han, Y. (1992). S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cr56n283p

Chicago Manual of Style (16th Edition):

Han, Yongxin. “S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones.” 1992. Doctoral Dissertation, University of Alberta. Accessed October 30, 2020. https://era.library.ualberta.ca/files/cr56n283p.

MLA Handbook (7th Edition):

Han, Yongxin. “S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones.” 1992. Web. 30 Oct 2020.

Vancouver:

Han Y. S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones. [Internet] [Doctoral dissertation]. University of Alberta; 1992. [cited 2020 Oct 30]. Available from: https://era.library.ualberta.ca/files/cr56n283p.

Council of Science Editors:

Han Y. S, S'-diethyl dithiomalonate as ethanol carbanion equivalent in annelation reactions and facial selectivity in Diels-Alder reaction of 4,4-disubstituted, 2,5-cyclohexadienones. [Doctoral Dissertation]. University of Alberta; 1992. Available from: https://era.library.ualberta.ca/files/cr56n283p


Loyola University Chicago

13. Qualizza, Brittni Qualizza. Exploring Conditions for the Enhancement of Acene Semiconductors Through the Use of the Diels-Alder Reaction.

Degree: PhD, Chemistry, 2016, Loyola University Chicago

  This dissertation demonstrates the application of SAMs to the surface of acene crystals, specifically of tetracene and rubrene, using the Diels-Alder reaction. The second… (more)

Subjects/Keywords: Acenes; Diels-Alder Reaction; Kinetics; Organic Semiconductors; Pentacene; Rubrene; Inorganic Chemistry

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APA (6th Edition):

Qualizza, B. Q. (2016). Exploring Conditions for the Enhancement of Acene Semiconductors Through the Use of the Diels-Alder Reaction. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/2292

Chicago Manual of Style (16th Edition):

Qualizza, Brittni Qualizza. “Exploring Conditions for the Enhancement of Acene Semiconductors Through the Use of the Diels-Alder Reaction.” 2016. Doctoral Dissertation, Loyola University Chicago. Accessed October 30, 2020. https://ecommons.luc.edu/luc_diss/2292.

MLA Handbook (7th Edition):

Qualizza, Brittni Qualizza. “Exploring Conditions for the Enhancement of Acene Semiconductors Through the Use of the Diels-Alder Reaction.” 2016. Web. 30 Oct 2020.

Vancouver:

Qualizza BQ. Exploring Conditions for the Enhancement of Acene Semiconductors Through the Use of the Diels-Alder Reaction. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2016. [cited 2020 Oct 30]. Available from: https://ecommons.luc.edu/luc_diss/2292.

Council of Science Editors:

Qualizza BQ. Exploring Conditions for the Enhancement of Acene Semiconductors Through the Use of the Diels-Alder Reaction. [Doctoral Dissertation]. Loyola University Chicago; 2016. Available from: https://ecommons.luc.edu/luc_diss/2292


Drexel University

14. Murray, James K., Jr. [alpha]-Nitrosulfones: Synthetic and mechanistic studies.

Degree: 2003, Drexel University

Three-α-substituted nitroethylene derivatives were prepared in situ from phenylsulfonylnitromethane, α-nitroacetophenone, and ethyl nitroacetate and allowed to react with a series of dienes to yield the… (more)

Subjects/Keywords: Nitro compounds; Diels-Alder reaction

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APA (6th Edition):

Murray, James K., J. (2003). [alpha]-Nitrosulfones: Synthetic and mechanistic studies. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/101

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):

Murray, James K., Jr. “[alpha]-Nitrosulfones: Synthetic and mechanistic studies.” 2003. Thesis, Drexel University. Accessed October 30, 2020. http://hdl.handle.net/1860/101.

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

MLA Handbook (7th Edition):

Murray, James K., Jr. “[alpha]-Nitrosulfones: Synthetic and mechanistic studies.” 2003. Web. 30 Oct 2020.

Vancouver:

Murray, James K. J. [alpha]-Nitrosulfones: Synthetic and mechanistic studies. [Internet] [Thesis]. Drexel University; 2003. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1860/101.

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

Council of Science Editors:

Murray, James K. J. [alpha]-Nitrosulfones: Synthetic and mechanistic studies. [Thesis]. Drexel University; 2003. Available from: http://hdl.handle.net/1860/101

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


University of Delaware

15. Nikbin, Nima. First-principles-based kinetic modeling of the zeolite-catalyzed conversion of furans to aromatics.

Degree: PhD, University of Delaware, Department of Chemical and Biomolecular Engineering, 2014, University of Delaware

 The development of strategies to convert renewable feedstocks into fuels and chemicals and displace petroleum is motivated from economic, environmental and political reasons and is… (more)

Subjects/Keywords: Furans.; Aromatic compounds  – Synthesis.; Diels-Alder reaction.; Acids.; Catalysis.; Zeolites.

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APA (6th Edition):

Nikbin, N. (2014). First-principles-based kinetic modeling of the zeolite-catalyzed conversion of furans to aromatics. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/16771

Chicago Manual of Style (16th Edition):

Nikbin, Nima. “First-principles-based kinetic modeling of the zeolite-catalyzed conversion of furans to aromatics.” 2014. Doctoral Dissertation, University of Delaware. Accessed October 30, 2020. http://udspace.udel.edu/handle/19716/16771.

MLA Handbook (7th Edition):

Nikbin, Nima. “First-principles-based kinetic modeling of the zeolite-catalyzed conversion of furans to aromatics.” 2014. Web. 30 Oct 2020.

Vancouver:

Nikbin N. First-principles-based kinetic modeling of the zeolite-catalyzed conversion of furans to aromatics. [Internet] [Doctoral dissertation]. University of Delaware; 2014. [cited 2020 Oct 30]. Available from: http://udspace.udel.edu/handle/19716/16771.

Council of Science Editors:

Nikbin N. First-principles-based kinetic modeling of the zeolite-catalyzed conversion of furans to aromatics. [Doctoral Dissertation]. University of Delaware; 2014. Available from: http://udspace.udel.edu/handle/19716/16771


Boston University

16. Qi, Chao. Total syntheses of prenylflavonoids and polyketide-derived natural products.

Degree: PhD, Chemistry, 2017, Boston University

 Concise syntheses of the natural products brosimones A and B have been achieved using sequential dehydrogenative Diels-Alder (DHDA) cycloadditions. The syntheses employ either Pt/C-cyclopentene or… (more)

Subjects/Keywords: Organic chemistry; Diels-Alder reaction; Silver nanoparticle; Total synthesis; Polyketide; Prenylflavonoids

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APA (6th Edition):

Qi, C. (2017). Total syntheses of prenylflavonoids and polyketide-derived natural products. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/20865

Chicago Manual of Style (16th Edition):

Qi, Chao. “Total syntheses of prenylflavonoids and polyketide-derived natural products.” 2017. Doctoral Dissertation, Boston University. Accessed October 30, 2020. http://hdl.handle.net/2144/20865.

MLA Handbook (7th Edition):

Qi, Chao. “Total syntheses of prenylflavonoids and polyketide-derived natural products.” 2017. Web. 30 Oct 2020.

Vancouver:

Qi C. Total syntheses of prenylflavonoids and polyketide-derived natural products. [Internet] [Doctoral dissertation]. Boston University; 2017. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2144/20865.

Council of Science Editors:

Qi C. Total syntheses of prenylflavonoids and polyketide-derived natural products. [Doctoral Dissertation]. Boston University; 2017. Available from: http://hdl.handle.net/2144/20865

17. Montagnon, T. Synthetic studies towards the squalestatins.

Degree: PhD, 2000, University of Sussex

Subjects/Keywords: 547; Diels Alder reaction; Furan

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APA (6th Edition):

Montagnon, T. (2000). Synthetic studies towards the squalestatins. (Doctoral Dissertation). University of Sussex. Retrieved from https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326933

Chicago Manual of Style (16th Edition):

Montagnon, T. “Synthetic studies towards the squalestatins.” 2000. Doctoral Dissertation, University of Sussex. Accessed October 30, 2020. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326933.

MLA Handbook (7th Edition):

Montagnon, T. “Synthetic studies towards the squalestatins.” 2000. Web. 30 Oct 2020.

Vancouver:

Montagnon T. Synthetic studies towards the squalestatins. [Internet] [Doctoral dissertation]. University of Sussex; 2000. [cited 2020 Oct 30]. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326933.

Council of Science Editors:

Montagnon T. Synthetic studies towards the squalestatins. [Doctoral Dissertation]. University of Sussex; 2000. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326933


Hong Kong University of Science and Technology

18. Lau, Patrick Chi Wai. Studies on Lewis acid-catalyzed intermolecular Diels-Alder cycloaddition of 1,1-dimethyl-1,3-butadiene derivatives and applications to taxoid synthesis.

Degree: 1997, Hong Kong University of Science and Technology

 The Diels-Alder cycloaddition reaction of 1,l-dimethyl-1,3-butadiene derivatives received less attention until the discovery of the potent anticancer drug, taxol, in which the A-ring fragment can… (more)

Subjects/Keywords: Diels-Alder reaction ; Paclitaxel

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APA (6th Edition):

Lau, P. C. W. (1997). Studies on Lewis acid-catalyzed intermolecular Diels-Alder cycloaddition of 1,1-dimethyl-1,3-butadiene derivatives and applications to taxoid synthesis. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-1474 ; https://doi.org/10.14711/thesis-b560402 ; http://repository.ust.hk/ir/bitstream/1783.1-1474/1/th_redirect.html

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):

Lau, Patrick Chi Wai. “Studies on Lewis acid-catalyzed intermolecular Diels-Alder cycloaddition of 1,1-dimethyl-1,3-butadiene derivatives and applications to taxoid synthesis.” 1997. Thesis, Hong Kong University of Science and Technology. Accessed October 30, 2020. http://repository.ust.hk/ir/Record/1783.1-1474 ; https://doi.org/10.14711/thesis-b560402 ; http://repository.ust.hk/ir/bitstream/1783.1-1474/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Lau, Patrick Chi Wai. “Studies on Lewis acid-catalyzed intermolecular Diels-Alder cycloaddition of 1,1-dimethyl-1,3-butadiene derivatives and applications to taxoid synthesis.” 1997. Web. 30 Oct 2020.

Vancouver:

Lau PCW. Studies on Lewis acid-catalyzed intermolecular Diels-Alder cycloaddition of 1,1-dimethyl-1,3-butadiene derivatives and applications to taxoid synthesis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 1997. [cited 2020 Oct 30]. Available from: http://repository.ust.hk/ir/Record/1783.1-1474 ; https://doi.org/10.14711/thesis-b560402 ; http://repository.ust.hk/ir/bitstream/1783.1-1474/1/th_redirect.html.

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

Council of Science Editors:

Lau PCW. Studies on Lewis acid-catalyzed intermolecular Diels-Alder cycloaddition of 1,1-dimethyl-1,3-butadiene derivatives and applications to taxoid synthesis. [Thesis]. Hong Kong University of Science and Technology; 1997. Available from: http://repository.ust.hk/ir/Record/1783.1-1474 ; https://doi.org/10.14711/thesis-b560402 ; http://repository.ust.hk/ir/bitstream/1783.1-1474/1/th_redirect.html

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


Michigan State University

19. McComb, Robert Eugene. The synthesis of the endothiobicyclo ring system by means of the Diels-Alder reaction.

Degree: PhD, Department of Chemistry, 1969, Michigan State University

Subjects/Keywords: Diels-Alder reaction; Cyclic compounds

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APA (6th Edition):

McComb, R. E. (1969). The synthesis of the endothiobicyclo ring system by means of the Diels-Alder reaction. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:35510

Chicago Manual of Style (16th Edition):

McComb, Robert Eugene. “The synthesis of the endothiobicyclo ring system by means of the Diels-Alder reaction.” 1969. Doctoral Dissertation, Michigan State University. Accessed October 30, 2020. http://etd.lib.msu.edu/islandora/object/etd:35510.

MLA Handbook (7th Edition):

McComb, Robert Eugene. “The synthesis of the endothiobicyclo ring system by means of the Diels-Alder reaction.” 1969. Web. 30 Oct 2020.

Vancouver:

McComb RE. The synthesis of the endothiobicyclo ring system by means of the Diels-Alder reaction. [Internet] [Doctoral dissertation]. Michigan State University; 1969. [cited 2020 Oct 30]. Available from: http://etd.lib.msu.edu/islandora/object/etd:35510.

Council of Science Editors:

McComb RE. The synthesis of the endothiobicyclo ring system by means of the Diels-Alder reaction. [Doctoral Dissertation]. Michigan State University; 1969. Available from: http://etd.lib.msu.edu/islandora/object/etd:35510


Michigan State University

20. Klipa, Dennis K. Part I, Extended hückel molecular orbital calculations of the relative stability of isotrindenetrione. Part II, Preparation of and estimation of the strain energy in the diels-alder dimers of two simple C-face annulated cyclopentadienones.

Degree: PhD, Department of Chemistry, 1981, Michigan State University

Subjects/Keywords: Diels-Alder reaction; Molecular orbitals

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APA (6th Edition):

Klipa, D. K. (1981). Part I, Extended hückel molecular orbital calculations of the relative stability of isotrindenetrione. Part II, Preparation of and estimation of the strain energy in the diels-alder dimers of two simple C-face annulated cyclopentadienones. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:35321

Chicago Manual of Style (16th Edition):

Klipa, Dennis K. “Part I, Extended hückel molecular orbital calculations of the relative stability of isotrindenetrione. Part II, Preparation of and estimation of the strain energy in the diels-alder dimers of two simple C-face annulated cyclopentadienones.” 1981. Doctoral Dissertation, Michigan State University. Accessed October 30, 2020. http://etd.lib.msu.edu/islandora/object/etd:35321.

MLA Handbook (7th Edition):

Klipa, Dennis K. “Part I, Extended hückel molecular orbital calculations of the relative stability of isotrindenetrione. Part II, Preparation of and estimation of the strain energy in the diels-alder dimers of two simple C-face annulated cyclopentadienones.” 1981. Web. 30 Oct 2020.

Vancouver:

Klipa DK. Part I, Extended hückel molecular orbital calculations of the relative stability of isotrindenetrione. Part II, Preparation of and estimation of the strain energy in the diels-alder dimers of two simple C-face annulated cyclopentadienones. [Internet] [Doctoral dissertation]. Michigan State University; 1981. [cited 2020 Oct 30]. Available from: http://etd.lib.msu.edu/islandora/object/etd:35321.

Council of Science Editors:

Klipa DK. Part I, Extended hückel molecular orbital calculations of the relative stability of isotrindenetrione. Part II, Preparation of and estimation of the strain energy in the diels-alder dimers of two simple C-face annulated cyclopentadienones. [Doctoral Dissertation]. Michigan State University; 1981. Available from: http://etd.lib.msu.edu/islandora/object/etd:35321


University of Minnesota

21. Gramlich, William Mike. Functionalized renewable polymers to toughen polylactide.

Degree: PhD, Chemical Engineering, 2012, University of Minnesota

 Sustainable polymers can overcome the limitations of petroleum sourced materials due to their renewable feedstocks, biodegradability, recyclability, and nontoxic nature. The renewably sourced polymer polylactide… (more)

Subjects/Keywords: Diels-Alder reaction; Graft copolymers; Melt blending; Polyisoprene; Polylactide; Radical copolymerization

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APA (6th Edition):

Gramlich, W. M. (2012). Functionalized renewable polymers to toughen polylactide. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/162812

Chicago Manual of Style (16th Edition):

Gramlich, William Mike. “Functionalized renewable polymers to toughen polylactide.” 2012. Doctoral Dissertation, University of Minnesota. Accessed October 30, 2020. http://hdl.handle.net/11299/162812.

MLA Handbook (7th Edition):

Gramlich, William Mike. “Functionalized renewable polymers to toughen polylactide.” 2012. Web. 30 Oct 2020.

Vancouver:

Gramlich WM. Functionalized renewable polymers to toughen polylactide. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11299/162812.

Council of Science Editors:

Gramlich WM. Functionalized renewable polymers to toughen polylactide. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://hdl.handle.net/11299/162812


University of Minnesota

22. Ross, Sean. Applications and Mechanistic Studies of the Hexadehydro-Diels–Alder Reaction.

Degree: PhD, Chemistry, 2017, University of Minnesota

 The ability to thermally generate benzynes via the cycloisomerization of a tethered alkyne with a conjugated diyne (the hexadehydro-Diels–Alder reaction) allows for the generation of… (more)

Subjects/Keywords: Hexadehydro-Diels–Alder reaction; Natural product functionalization; Three-component reactions

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APA (6th Edition):

Ross, S. (2017). Applications and Mechanistic Studies of the Hexadehydro-Diels–Alder Reaction. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/211320

Chicago Manual of Style (16th Edition):

Ross, Sean. “Applications and Mechanistic Studies of the Hexadehydro-Diels–Alder Reaction.” 2017. Doctoral Dissertation, University of Minnesota. Accessed October 30, 2020. http://hdl.handle.net/11299/211320.

MLA Handbook (7th Edition):

Ross, Sean. “Applications and Mechanistic Studies of the Hexadehydro-Diels–Alder Reaction.” 2017. Web. 30 Oct 2020.

Vancouver:

Ross S. Applications and Mechanistic Studies of the Hexadehydro-Diels–Alder Reaction. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11299/211320.

Council of Science Editors:

Ross S. Applications and Mechanistic Studies of the Hexadehydro-Diels–Alder Reaction. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/211320

23. Silber, Ernesto. Solvent Effects in the Diels Alder Reaction.

Degree: Chemistry, 1971, Texas Tech University

Subjects/Keywords: Diels-Alder reaction; Solvents

…At the present time, only two stud- ies of solvent effects in the Diels-Alder reaction… …historical review of the Diels-Alder is made in Chapter II. reaction Chapter III presents a… …Reaction The first mechanistic studies of the Diels-Alder reaction concerned the dimerization of… …isomeric products [ 1 9 ] . Theoretical Approach to the Diels-Alder Reaction Molecular… …products of the reaction [19]. 8. Diels-Alder reactions are catalyzed by Lewis acids… 

Page 1 Page 2 Page 3 Page 4 Page 5

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APA (6th Edition):

Silber, E. (1971). Solvent Effects in the Diels Alder Reaction. (Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/21872

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):

Silber, Ernesto. “Solvent Effects in the Diels Alder Reaction.” 1971. Thesis, Texas Tech University. Accessed October 30, 2020. http://hdl.handle.net/2346/21872.

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

MLA Handbook (7th Edition):

Silber, Ernesto. “Solvent Effects in the Diels Alder Reaction.” 1971. Web. 30 Oct 2020.

Vancouver:

Silber E. Solvent Effects in the Diels Alder Reaction. [Internet] [Thesis]. Texas Tech University; 1971. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2346/21872.

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

Council of Science Editors:

Silber E. Solvent Effects in the Diels Alder Reaction. [Thesis]. Texas Tech University; 1971. Available from: http://hdl.handle.net/2346/21872

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


University of Hong Kong

24. Chan, Tin-yau. A synthetic approach to Yuehchukene analogues.

Degree: 1987, University of Hong Kong

Subjects/Keywords: Diels-Alder reaction.; Alkaloids - Synthesis.

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APA (6th Edition):

Chan, T. (1987). A synthetic approach to Yuehchukene analogues. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/32441

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):

Chan, Tin-yau. “A synthetic approach to Yuehchukene analogues.” 1987. Thesis, University of Hong Kong. Accessed October 30, 2020. http://hdl.handle.net/10722/32441.

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

MLA Handbook (7th Edition):

Chan, Tin-yau. “A synthetic approach to Yuehchukene analogues.” 1987. Web. 30 Oct 2020.

Vancouver:

Chan T. A synthetic approach to Yuehchukene analogues. [Internet] [Thesis]. University of Hong Kong; 1987. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10722/32441.

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

Council of Science Editors:

Chan T. A synthetic approach to Yuehchukene analogues. [Thesis]. University of Hong Kong; 1987. Available from: http://hdl.handle.net/10722/32441

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


Georgia Tech

25. Wozniak, John C. Preparation and reactions of Diels-Alder adducts of lignin-derived quinones.

Degree: PhD, Institute of Paper Science and Technology, 1988, Georgia Tech

Subjects/Keywords: Quinone; Diels-Alder reaction

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APA (6th Edition):

Wozniak, J. C. (1988). Preparation and reactions of Diels-Alder adducts of lignin-derived quinones. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/5515

Chicago Manual of Style (16th Edition):

Wozniak, John C. “Preparation and reactions of Diels-Alder adducts of lignin-derived quinones.” 1988. Doctoral Dissertation, Georgia Tech. Accessed October 30, 2020. http://hdl.handle.net/1853/5515.

MLA Handbook (7th Edition):

Wozniak, John C. “Preparation and reactions of Diels-Alder adducts of lignin-derived quinones.” 1988. Web. 30 Oct 2020.

Vancouver:

Wozniak JC. Preparation and reactions of Diels-Alder adducts of lignin-derived quinones. [Internet] [Doctoral dissertation]. Georgia Tech; 1988. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1853/5515.

Council of Science Editors:

Wozniak JC. Preparation and reactions of Diels-Alder adducts of lignin-derived quinones. [Doctoral Dissertation]. Georgia Tech; 1988. Available from: http://hdl.handle.net/1853/5515


University of Central Florida

26. Banerjee, Siddthartha. Photo Retro Diels-alder Reaction Of The Adducts Of Tetracyanoethylene And Polyaromatic Compounds.

Degree: 2011, University of Central Florida

 Thermally induced retro-Diels Alder (rDA) reaction has been extensively used for the preparation of many reactive intermediates in organic synthesis. But the uses of photo-retro… (more)

Subjects/Keywords: Diels Alder reaction; Chemistry; Dissertations, Academic  – Sciences, Sciences  – Dissertations, Academic

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APA (6th Edition):

Banerjee, S. (2011). Photo Retro Diels-alder Reaction Of The Adducts Of Tetracyanoethylene And Polyaromatic Compounds. (Masters Thesis). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/1899

Chicago Manual of Style (16th Edition):

Banerjee, Siddthartha. “Photo Retro Diels-alder Reaction Of The Adducts Of Tetracyanoethylene And Polyaromatic Compounds.” 2011. Masters Thesis, University of Central Florida. Accessed October 30, 2020. https://stars.library.ucf.edu/etd/1899.

MLA Handbook (7th Edition):

Banerjee, Siddthartha. “Photo Retro Diels-alder Reaction Of The Adducts Of Tetracyanoethylene And Polyaromatic Compounds.” 2011. Web. 30 Oct 2020.

Vancouver:

Banerjee S. Photo Retro Diels-alder Reaction Of The Adducts Of Tetracyanoethylene And Polyaromatic Compounds. [Internet] [Masters thesis]. University of Central Florida; 2011. [cited 2020 Oct 30]. Available from: https://stars.library.ucf.edu/etd/1899.

Council of Science Editors:

Banerjee S. Photo Retro Diels-alder Reaction Of The Adducts Of Tetracyanoethylene And Polyaromatic Compounds. [Masters Thesis]. University of Central Florida; 2011. Available from: https://stars.library.ucf.edu/etd/1899


University of Cambridge

27. Birkinshaw, Timothy Nicholas. Diels-Alder routes to Prosopis alkaloids.

Degree: PhD, 1987, University of Cambridge

 This thesis describes the investigation of the Diels-Alder reaction of the imine (140) with the diene (141) to give four products (142,143,156, 157). At low… (more)

Subjects/Keywords: 547; Imino Diels-Alder reaction

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APA (6th Edition):

Birkinshaw, T. N. (1987). Diels-Alder routes to Prosopis alkaloids. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.17292 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233716

Chicago Manual of Style (16th Edition):

Birkinshaw, Timothy Nicholas. “Diels-Alder routes to Prosopis alkaloids.” 1987. Doctoral Dissertation, University of Cambridge. Accessed October 30, 2020. https://doi.org/10.17863/CAM.17292 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233716.

MLA Handbook (7th Edition):

Birkinshaw, Timothy Nicholas. “Diels-Alder routes to Prosopis alkaloids.” 1987. Web. 30 Oct 2020.

Vancouver:

Birkinshaw TN. Diels-Alder routes to Prosopis alkaloids. [Internet] [Doctoral dissertation]. University of Cambridge; 1987. [cited 2020 Oct 30]. Available from: https://doi.org/10.17863/CAM.17292 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233716.

Council of Science Editors:

Birkinshaw TN. Diels-Alder routes to Prosopis alkaloids. [Doctoral Dissertation]. University of Cambridge; 1987. Available from: https://doi.org/10.17863/CAM.17292 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233716


University of British Columbia

28. Friesen, Richard William. Annulations leading to bicyclic dienes : Diels-Alder reactions of (some of) the dienes and dolastane diterpenoid syntheses.

Degree: PhD, Chemistry, 1988, University of British Columbia

 The preparation of bicyclic dienes of the general structures (72), (82), (83) and (162) is described. These materials have been prepared via a novel annulation… (more)

Subjects/Keywords: Diolefins  – Synthesis; Diels-Alder reaction

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APA (6th Edition):

Friesen, R. W. (1988). Annulations leading to bicyclic dienes : Diels-Alder reactions of (some of) the dienes and dolastane diterpenoid syntheses. (Doctoral Dissertation). University of British Columbia. Retrieved from http://hdl.handle.net/2429/28781

Chicago Manual of Style (16th Edition):

Friesen, Richard William. “Annulations leading to bicyclic dienes : Diels-Alder reactions of (some of) the dienes and dolastane diterpenoid syntheses.” 1988. Doctoral Dissertation, University of British Columbia. Accessed October 30, 2020. http://hdl.handle.net/2429/28781.

MLA Handbook (7th Edition):

Friesen, Richard William. “Annulations leading to bicyclic dienes : Diels-Alder reactions of (some of) the dienes and dolastane diterpenoid syntheses.” 1988. Web. 30 Oct 2020.

Vancouver:

Friesen RW. Annulations leading to bicyclic dienes : Diels-Alder reactions of (some of) the dienes and dolastane diterpenoid syntheses. [Internet] [Doctoral dissertation]. University of British Columbia; 1988. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2429/28781.

Council of Science Editors:

Friesen RW. Annulations leading to bicyclic dienes : Diels-Alder reactions of (some of) the dienes and dolastane diterpenoid syntheses. [Doctoral Dissertation]. University of British Columbia; 1988. Available from: http://hdl.handle.net/2429/28781


University of British Columbia

29. Stone, Charles. Preparation and reactivity of heterosubstituted 1,3-Dienes.

Degree: PhD, Chemistry, 1988, University of British Columbia

 The chemoselective hydrozirconation reaction of a series of 1-ene-3-yne molecules 51a-d, using the commercially available hydride reagent, Cp₂ZrCl(H) 1, provides an efficient route to the… (more)

Subjects/Keywords: Diels-Alder reaction; Organometallic compounds

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APA (6th Edition):

Stone, C. (1988). Preparation and reactivity of heterosubstituted 1,3-Dienes. (Doctoral Dissertation). University of British Columbia. Retrieved from http://hdl.handle.net/2429/29433

Chicago Manual of Style (16th Edition):

Stone, Charles. “Preparation and reactivity of heterosubstituted 1,3-Dienes.” 1988. Doctoral Dissertation, University of British Columbia. Accessed October 30, 2020. http://hdl.handle.net/2429/29433.

MLA Handbook (7th Edition):

Stone, Charles. “Preparation and reactivity of heterosubstituted 1,3-Dienes.” 1988. Web. 30 Oct 2020.

Vancouver:

Stone C. Preparation and reactivity of heterosubstituted 1,3-Dienes. [Internet] [Doctoral dissertation]. University of British Columbia; 1988. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2429/29433.

Council of Science Editors:

Stone C. Preparation and reactivity of heterosubstituted 1,3-Dienes. [Doctoral Dissertation]. University of British Columbia; 1988. Available from: http://hdl.handle.net/2429/29433


University of British Columbia

30. Jennings, Barry Michael. Conformational effects in the photochemistry of tetrahydro-1,4-naphthoquinones.

Degree: PhD, Chemistry, 1975, University of British Columbia

 The photochemistry of a variety of tetrahydro-1,4-naphthoquinones (structure 1) has been investigated. These were synthesized by Diels-Alder reaction of corresponding p-quinones and acyclic-1,3-dienes [diagram omitted].… (more)

Subjects/Keywords: Photochemistry; Diels-Alder reaction

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

APA (6th Edition):

Jennings, B. M. (1975). Conformational effects in the photochemistry of tetrahydro-1,4-naphthoquinones. (Doctoral Dissertation). University of British Columbia. Retrieved from http://hdl.handle.net/2429/19739

Chicago Manual of Style (16th Edition):

Jennings, Barry Michael. “Conformational effects in the photochemistry of tetrahydro-1,4-naphthoquinones.” 1975. Doctoral Dissertation, University of British Columbia. Accessed October 30, 2020. http://hdl.handle.net/2429/19739.

MLA Handbook (7th Edition):

Jennings, Barry Michael. “Conformational effects in the photochemistry of tetrahydro-1,4-naphthoquinones.” 1975. Web. 30 Oct 2020.

Vancouver:

Jennings BM. Conformational effects in the photochemistry of tetrahydro-1,4-naphthoquinones. [Internet] [Doctoral dissertation]. University of British Columbia; 1975. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2429/19739.

Council of Science Editors:

Jennings BM. Conformational effects in the photochemistry of tetrahydro-1,4-naphthoquinones. [Doctoral Dissertation]. University of British Columbia; 1975. Available from: http://hdl.handle.net/2429/19739

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