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You searched for subject:(Diels Alder). Showing records 1 – 30 of 458 total matches.

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University of Melbourne

1. GUNAWAN, CHRISTIAN. Studies towards the synthesis of mulberry Diels-Alder adducts.

Degree: 2011, University of Melbourne

 The synthetic studies of mulberry Diels-Alder adducts are described. Two dehydroprenylarylbenzofuran adducts, mulberrofuran C hexamethyl ether (325) and mulberrofuran J hexamethyl ether (326) were obtained… (more)

Subjects/Keywords: Diels-Alder; synthesis

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APA (6th Edition):

GUNAWAN, C. (2011). Studies towards the synthesis of mulberry Diels-Alder adducts. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/36621

Chicago Manual of Style (16th Edition):

GUNAWAN, CHRISTIAN. “Studies towards the synthesis of mulberry Diels-Alder adducts.” 2011. Doctoral Dissertation, University of Melbourne. Accessed February 27, 2021. http://hdl.handle.net/11343/36621.

MLA Handbook (7th Edition):

GUNAWAN, CHRISTIAN. “Studies towards the synthesis of mulberry Diels-Alder adducts.” 2011. Web. 27 Feb 2021.

Vancouver:

GUNAWAN C. Studies towards the synthesis of mulberry Diels-Alder adducts. [Internet] [Doctoral dissertation]. University of Melbourne; 2011. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/11343/36621.

Council of Science Editors:

GUNAWAN C. Studies towards the synthesis of mulberry Diels-Alder adducts. [Doctoral Dissertation]. University of Melbourne; 2011. Available from: http://hdl.handle.net/11343/36621


Oregon State University

2. 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 February 27, 2021. 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. 27 Feb 2021.

Vancouver:

Schwartz JP. Expanding the scope of a Diels-Alder approach to biaryl synthesis. [Internet] [Doctoral dissertation]. Oregon State University; 2009. [cited 2021 Feb 27]. 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


UCLA

3. Levandowski, Brian. Diels-Alder Reactivities of Cyclic Dienes and Dienophiles.

Degree: Chemistry, 2018, UCLA

 Since the discovery of the Diels-Alder reaction in 1928, chemical theorists have pursued a deeper understanding of the factors controlling reactivity and stereoselectivity for this… (more)

Subjects/Keywords: Computational chemistry; Diels-Alder

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APA (6th Edition):

Levandowski, B. (2018). Diels-Alder Reactivities of Cyclic Dienes and Dienophiles. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/22g6878g

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):

Levandowski, Brian. “Diels-Alder Reactivities of Cyclic Dienes and Dienophiles.” 2018. Thesis, UCLA. Accessed February 27, 2021. http://www.escholarship.org/uc/item/22g6878g.

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

MLA Handbook (7th Edition):

Levandowski, Brian. “Diels-Alder Reactivities of Cyclic Dienes and Dienophiles.” 2018. Web. 27 Feb 2021.

Vancouver:

Levandowski B. Diels-Alder Reactivities of Cyclic Dienes and Dienophiles. [Internet] [Thesis]. UCLA; 2018. [cited 2021 Feb 27]. Available from: http://www.escholarship.org/uc/item/22g6878g.

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

Council of Science Editors:

Levandowski B. Diels-Alder Reactivities of Cyclic Dienes and Dienophiles. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/22g6878g

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


Texas A&M University

4. Abbasov, Mikail Eminovich. Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application.

Degree: PhD, Chemistry, 2015, Texas A&M University

 Following the turn of the millennium, the role of asymmetric covalent organocatalysis has developed into a scalable, synthetic paradigm galvanizing the synthetic community toward utilization… (more)

Subjects/Keywords: Diels–Alder; Organocatalysis; Organocascade; Acylammonium

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APA (6th Edition):

Abbasov, M. E. (2015). Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187468

Chicago Manual of Style (16th Edition):

Abbasov, Mikail Eminovich. “Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application.” 2015. Doctoral Dissertation, Texas A&M University. Accessed February 27, 2021. http://hdl.handle.net/1969.1/187468.

MLA Handbook (7th Edition):

Abbasov, Mikail Eminovich. “Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application.” 2015. Web. 27 Feb 2021.

Vancouver:

Abbasov ME. Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/1969.1/187468.

Council of Science Editors:

Abbasov ME. Diels–Alder–Initiated Organocascades Employing Acylammonium Catalysis: Scope, Mechanism, and Application. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/187468


University of Guelph

5. Nikoloska, Irena. Towards the Synthesis of Novel PARP Inhibitors through Diels-Alder Chemistry.

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

 Poly(ADP-ribose) polymerase (PARP) represents a large family of enzymes that are activated upon DNA breakage, which are then involved in a cascade of reactions that… (more)

Subjects/Keywords: PARP; Diels-Alder; isoindolinone

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APA (6th Edition):

Nikoloska, I. (2012). Towards the Synthesis of Novel PARP Inhibitors through Diels-Alder Chemistry. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3561

Chicago Manual of Style (16th Edition):

Nikoloska, Irena. “Towards the Synthesis of Novel PARP Inhibitors through Diels-Alder Chemistry.” 2012. Masters Thesis, University of Guelph. Accessed February 27, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3561.

MLA Handbook (7th Edition):

Nikoloska, Irena. “Towards the Synthesis of Novel PARP Inhibitors through Diels-Alder Chemistry.” 2012. Web. 27 Feb 2021.

Vancouver:

Nikoloska I. Towards the Synthesis of Novel PARP Inhibitors through Diels-Alder Chemistry. [Internet] [Masters thesis]. University of Guelph; 2012. [cited 2021 Feb 27]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3561.

Council of Science Editors:

Nikoloska I. Towards the Synthesis of Novel PARP Inhibitors through Diels-Alder Chemistry. [Masters Thesis]. University of Guelph; 2012. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3561


Universidad Andrés Bello

6. Valenzuela Duarte, Joel Andrés. Criterios de sincronía/asincronía en mecanismos de reacciones de Diels-Alder: geometría, transferencia de carga y constante de fuerza de reacción .

Degree: 2015, Universidad Andrés Bello

 El proyecto que se presenta en esta Unidad de Investigación abarca un estudio teórico y computacional sobre criterios de sincronía/asincronía en mecanismos de las reacciones… (more)

Subjects/Keywords: Reacción de Diels-Alder

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APA (6th Edition):

Valenzuela Duarte, J. A. (2015). Criterios de sincronía/asincronía en mecanismos de reacciones de Diels-Alder: geometría, transferencia de carga y constante de fuerza de reacción . (Thesis). Universidad Andrés Bello. Retrieved from http://repositorio.unab.cl/xmlui/handle/ria/3582

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):

Valenzuela Duarte, Joel Andrés. “Criterios de sincronía/asincronía en mecanismos de reacciones de Diels-Alder: geometría, transferencia de carga y constante de fuerza de reacción .” 2015. Thesis, Universidad Andrés Bello. Accessed February 27, 2021. http://repositorio.unab.cl/xmlui/handle/ria/3582.

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

MLA Handbook (7th Edition):

Valenzuela Duarte, Joel Andrés. “Criterios de sincronía/asincronía en mecanismos de reacciones de Diels-Alder: geometría, transferencia de carga y constante de fuerza de reacción .” 2015. Web. 27 Feb 2021.

Vancouver:

Valenzuela Duarte JA. Criterios de sincronía/asincronía en mecanismos de reacciones de Diels-Alder: geometría, transferencia de carga y constante de fuerza de reacción . [Internet] [Thesis]. Universidad Andrés Bello; 2015. [cited 2021 Feb 27]. Available from: http://repositorio.unab.cl/xmlui/handle/ria/3582.

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

Council of Science Editors:

Valenzuela Duarte JA. Criterios de sincronía/asincronía en mecanismos de reacciones de Diels-Alder: geometría, transferencia de carga y constante de fuerza de reacción . [Thesis]. Universidad Andrés Bello; 2015. Available from: http://repositorio.unab.cl/xmlui/handle/ria/3582

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


University of New South Wales

7. Reed, John. Application of the Diels-Alder Reaction to the Synthesis of Natural Product-like Libraries.

Degree: Chemistry, 2017, University of New South Wales

 This thesis is focussed on the use of the diene-regenerative Diels-Alder reaction to assemble bicyclic molecular frameworks that are commonly found in bioactive natural products.… (more)

Subjects/Keywords: Compound Libraries; Diels-Alder; Synthesis

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APA (6th Edition):

Reed, J. (2017). Application of the Diels-Alder Reaction to the Synthesis of Natural Product-like Libraries. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/57222 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42862/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Reed, John. “Application of the Diels-Alder Reaction to the Synthesis of Natural Product-like Libraries.” 2017. Masters Thesis, University of New South Wales. Accessed February 27, 2021. http://handle.unsw.edu.au/1959.4/57222 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42862/SOURCE02?view=true.

MLA Handbook (7th Edition):

Reed, John. “Application of the Diels-Alder Reaction to the Synthesis of Natural Product-like Libraries.” 2017. Web. 27 Feb 2021.

Vancouver:

Reed J. Application of the Diels-Alder Reaction to the Synthesis of Natural Product-like Libraries. [Internet] [Masters thesis]. University of New South Wales; 2017. [cited 2021 Feb 27]. Available from: http://handle.unsw.edu.au/1959.4/57222 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42862/SOURCE02?view=true.

Council of Science Editors:

Reed J. Application of the Diels-Alder Reaction to the Synthesis of Natural Product-like Libraries. [Masters Thesis]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/57222 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42862/SOURCE02?view=true

8. Carmichael, Rachael A. One-pot Tandem Diels-Alder/Nazarov Reactions to Generate Advanced Tricyclic Intermediates.

Degree: 2017, University of Nevada – Reno

 One-pot multi-component reactions represent efficacious strategies to rapidly obtain complex intermediates applicable in the synthesis of therapeutically germane compounds. Nazarov reactions of aryl vinyl ketones… (more)

Subjects/Keywords: cascade; Diels-Alder; Nazarov; tandem

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APA (6th Edition):

Carmichael, R. A. (2017). One-pot Tandem Diels-Alder/Nazarov Reactions to Generate Advanced Tricyclic Intermediates. (Thesis). University of Nevada – Reno. Retrieved from http://hdl.handle.net/11714/2088

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):

Carmichael, Rachael A. “One-pot Tandem Diels-Alder/Nazarov Reactions to Generate Advanced Tricyclic Intermediates.” 2017. Thesis, University of Nevada – Reno. Accessed February 27, 2021. http://hdl.handle.net/11714/2088.

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

MLA Handbook (7th Edition):

Carmichael, Rachael A. “One-pot Tandem Diels-Alder/Nazarov Reactions to Generate Advanced Tricyclic Intermediates.” 2017. Web. 27 Feb 2021.

Vancouver:

Carmichael RA. One-pot Tandem Diels-Alder/Nazarov Reactions to Generate Advanced Tricyclic Intermediates. [Internet] [Thesis]. University of Nevada – Reno; 2017. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/11714/2088.

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

Council of Science Editors:

Carmichael RA. One-pot Tandem Diels-Alder/Nazarov Reactions to Generate Advanced Tricyclic Intermediates. [Thesis]. University of Nevada – Reno; 2017. Available from: http://hdl.handle.net/11714/2088

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


King Abdullah University of Science and Technology

9. Fischer, Johannes. A Pathway to Artificial Metalloenzymes.

Degree: Biological and Environmental Sciences and Engineering (BESE) Division, 2015, King Abdullah University of Science and Technology

 The advancement of catalytic systems and the application thereof has proven to be the key to overcome traditional limitations of industrial-scale synthetic processes. Converging organometallic… (more)

Subjects/Keywords: Metalloenzymes; fluorescent protein; Diels-Alder

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APA (6th Edition):

Fischer, J. (2015). A Pathway to Artificial Metalloenzymes. (Thesis). King Abdullah University of Science and Technology. Retrieved from http://hdl.handle.net/10754/583809

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):

Fischer, Johannes. “A Pathway to Artificial Metalloenzymes.” 2015. Thesis, King Abdullah University of Science and Technology. Accessed February 27, 2021. http://hdl.handle.net/10754/583809.

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

MLA Handbook (7th Edition):

Fischer, Johannes. “A Pathway to Artificial Metalloenzymes.” 2015. Web. 27 Feb 2021.

Vancouver:

Fischer J. A Pathway to Artificial Metalloenzymes. [Internet] [Thesis]. King Abdullah University of Science and Technology; 2015. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/10754/583809.

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

Council of Science Editors:

Fischer J. A Pathway to Artificial Metalloenzymes. [Thesis]. King Abdullah University of Science and Technology; 2015. Available from: http://hdl.handle.net/10754/583809

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

10. 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 February 27, 2021. 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. 27 Feb 2021.

Vancouver:

Barbosa JdS. Estudo sobre a síntese de furanoliangolidos pela Reação de Diels-Alder. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2021 Feb 27]. 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/ ;

11. Froidevaux, Vincent. Réticulation de polymères polysulfure par réaction thiol-Michaël contrôlée : Polysulfide polymers Crosslinking by a controlled thiol-Michaël reaction.

Degree: Docteur es, Chimie des matériaux, 2014, Montpellier, Ecole nationale supérieure de chimie

 Les mastics polysulfures sont très utilisés dans l'aéronautique, ceci grâce à leur bonne tenue au froid et leur résistance au carburant. La plupart d'entre eux… (more)

Subjects/Keywords: Réticulation; Polysulfure; Thiol-Michaël; Scod; Diels-Alder; RétroDiels-Alder; Crosslinking; Polysulfide; Thiol-Michaël; Scod; Diels-Alder; RetroDiels-Alder; 540

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APA (6th Edition):

Froidevaux, V. (2014). Réticulation de polymères polysulfure par réaction thiol-Michaël contrôlée : Polysulfide polymers Crosslinking by a controlled thiol-Michaël reaction. (Doctoral Dissertation). Montpellier, Ecole nationale supérieure de chimie. Retrieved from http://www.theses.fr/2014ENCM0009

Chicago Manual of Style (16th Edition):

Froidevaux, Vincent. “Réticulation de polymères polysulfure par réaction thiol-Michaël contrôlée : Polysulfide polymers Crosslinking by a controlled thiol-Michaël reaction.” 2014. Doctoral Dissertation, Montpellier, Ecole nationale supérieure de chimie. Accessed February 27, 2021. http://www.theses.fr/2014ENCM0009.

MLA Handbook (7th Edition):

Froidevaux, Vincent. “Réticulation de polymères polysulfure par réaction thiol-Michaël contrôlée : Polysulfide polymers Crosslinking by a controlled thiol-Michaël reaction.” 2014. Web. 27 Feb 2021.

Vancouver:

Froidevaux V. Réticulation de polymères polysulfure par réaction thiol-Michaël contrôlée : Polysulfide polymers Crosslinking by a controlled thiol-Michaël reaction. [Internet] [Doctoral dissertation]. Montpellier, Ecole nationale supérieure de chimie; 2014. [cited 2021 Feb 27]. Available from: http://www.theses.fr/2014ENCM0009.

Council of Science Editors:

Froidevaux V. Réticulation de polymères polysulfure par réaction thiol-Michaël contrôlée : Polysulfide polymers Crosslinking by a controlled thiol-Michaël reaction. [Doctoral Dissertation]. Montpellier, Ecole nationale supérieure de chimie; 2014. Available from: http://www.theses.fr/2014ENCM0009


UCLA

12. LIU, FANG. Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines.

Degree: Chemistry, 2014, UCLA

 The concept of gating was introduced into host-guest chemistry by our group in the 1990s, as a result of computational studies on Cram's hemicarcerands. Since… (more)

Subjects/Keywords: Chemistry; Diels-Alder reactions; Gating; Hemicarcerands; Tetrazines

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APA (6th Edition):

LIU, F. (2014). Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6028d3n8

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):

LIU, FANG. “Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines.” 2014. Thesis, UCLA. Accessed February 27, 2021. http://www.escholarship.org/uc/item/6028d3n8.

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

MLA Handbook (7th Edition):

LIU, FANG. “Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines.” 2014. Web. 27 Feb 2021.

Vancouver:

LIU F. Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines. [Internet] [Thesis]. UCLA; 2014. [cited 2021 Feb 27]. Available from: http://www.escholarship.org/uc/item/6028d3n8.

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

Council of Science Editors:

LIU F. Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/6028d3n8

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


Universidade do Rio Grande do Norte

13. Monteiro, Norberto de Kássio Vieira. Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos .

Degree: 2015, Universidade do Rio Grande do Norte

 This thesis was performed in four chapters, at the theoretical level, focused mainly on electronic density. In the first chapter, we have applied an undergraduate… (more)

Subjects/Keywords: Diels-Alder; Ligação H-H; Tetraedrano; CYP17

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APA (6th Edition):

Monteiro, N. d. K. V. (2015). Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos . (Thesis). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/20755

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):

Monteiro, Norberto de Kássio Vieira. “Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos .” 2015. Thesis, Universidade do Rio Grande do Norte. Accessed February 27, 2021. http://repositorio.ufrn.br/handle/123456789/20755.

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

MLA Handbook (7th Edition):

Monteiro, Norberto de Kássio Vieira. “Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos .” 2015. Web. 27 Feb 2021.

Vancouver:

Monteiro NdKV. Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos . [Internet] [Thesis]. Universidade do Rio Grande do Norte; 2015. [cited 2021 Feb 27]. Available from: http://repositorio.ufrn.br/handle/123456789/20755.

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

Council of Science Editors:

Monteiro NdKV. Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos . [Thesis]. Universidade do Rio Grande do Norte; 2015. Available from: http://repositorio.ufrn.br/handle/123456789/20755

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


Universidade do Rio Grande do Norte

14. Monteiro, Norberto de Kássio Vieira. Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos .

Degree: 2015, Universidade do Rio Grande do Norte

 This thesis was performed in four chapters, at the theoretical level, focused mainly on electronic density. In the first chapter, we have applied an undergraduate… (more)

Subjects/Keywords: Diels-Alder; Ligação H-H; Tetraedrano; CYP17

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APA (6th Edition):

Monteiro, N. d. K. V. (2015). Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos . (Doctoral Dissertation). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/20755

Chicago Manual of Style (16th Edition):

Monteiro, Norberto de Kássio Vieira. “Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos .” 2015. Doctoral Dissertation, Universidade do Rio Grande do Norte. Accessed February 27, 2021. http://repositorio.ufrn.br/handle/123456789/20755.

MLA Handbook (7th Edition):

Monteiro, Norberto de Kássio Vieira. “Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos .” 2015. Web. 27 Feb 2021.

Vancouver:

Monteiro NdKV. Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos . [Internet] [Doctoral dissertation]. Universidade do Rio Grande do Norte; 2015. [cited 2021 Feb 27]. Available from: http://repositorio.ufrn.br/handle/123456789/20755.

Council of Science Editors:

Monteiro NdKV. Novos protocolos teóricos utilizados nos estudos das ligações hidrogênio-hidrogênio, na estabilidade do tetraedrano, seus derivados e das reações de diels-alder e na quantificação da afinidade de fármacos . [Doctoral Dissertation]. Universidade do Rio Grande do Norte; 2015. Available from: http://repositorio.ufrn.br/handle/123456789/20755


Oregon State University

15. 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 February 27, 2021. 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. 27 Feb 2021.

Vancouver:

Dei Rossi DR. The use of the Diels-Alder reaction in asymmetric synthesis. [Internet] [Masters thesis]. Oregon State University; 1978. [cited 2021 Feb 27]. 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

16. Maria Carolina Donatoni. A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas.

Degree: 2008, Universidade Federal de São Carlos

Neste trabalho foi feito um estudo do efeito das microondas sobre a reação de Diels - Alder das p-benzoquinonas timoquinona (A1), 2,5-dimetil-p-benzoquinona (A2) e 2,6-dimetil-p-benzoquinona… (more)

Subjects/Keywords: Diels-Alder; Microondas; Para-Benzoquinonas; QUIMICA

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APA (6th Edition):

Donatoni, M. C. (2008). A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas. (Thesis). Universidade Federal de São Carlos. Retrieved from http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=2667

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):

Donatoni, Maria Carolina. “A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas.” 2008. Thesis, Universidade Federal de São Carlos. Accessed February 27, 2021. http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=2667.

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

MLA Handbook (7th Edition):

Donatoni, Maria Carolina. “A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas.” 2008. Web. 27 Feb 2021.

Vancouver:

Donatoni MC. A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas. [Internet] [Thesis]. Universidade Federal de São Carlos; 2008. [cited 2021 Feb 27]. Available from: http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=2667.

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

Council of Science Editors:

Donatoni MC. A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas. [Thesis]. Universidade Federal de São Carlos; 2008. Available from: http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=2667

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


University of Houston

17. Li, Chien-hung 1986-. Plasmonic Nanoshells: Synthesis, Functionalization, and Photonic Applications.

Degree: PhD, Chemistry, 2015, University of Houston

 The work presented in this dissertation focuses on the functionalization and application of hollow gold-silver nanoshells (GS-NSs). GS-NSs were chosen for this research because of… (more)

Subjects/Keywords: Plasmonic; Hollow Gold-Silver Nanoshells; Diels-Alder

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APA (6th Edition):

Li, C. 1. (2015). Plasmonic Nanoshells: Synthesis, Functionalization, and Photonic Applications. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/6553

Chicago Manual of Style (16th Edition):

Li, Chien-hung 1986-. “Plasmonic Nanoshells: Synthesis, Functionalization, and Photonic Applications.” 2015. Doctoral Dissertation, University of Houston. Accessed February 27, 2021. http://hdl.handle.net/10657/6553.

MLA Handbook (7th Edition):

Li, Chien-hung 1986-. “Plasmonic Nanoshells: Synthesis, Functionalization, and Photonic Applications.” 2015. Web. 27 Feb 2021.

Vancouver:

Li C1. Plasmonic Nanoshells: Synthesis, Functionalization, and Photonic Applications. [Internet] [Doctoral dissertation]. University of Houston; 2015. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/10657/6553.

Council of Science Editors:

Li C1. Plasmonic Nanoshells: Synthesis, Functionalization, and Photonic Applications. [Doctoral Dissertation]. University of Houston; 2015. Available from: http://hdl.handle.net/10657/6553


University of Debrecen

18. Makrai, Andrea. Diels-Alder adduktot tartalmazó poliuretánok előállítása és vizsgálata .

Degree: DE – Természettudományi és Technológiai Kar – Kémiai Intézet, University of Debrecen

 A kutatócsoport előzetes munkái és az irodalmi áttekintés alapján célul tűztem ki új típusú, nagy molekulatömegű poli(-kaprolakton)-t és kis molekulájú láncnövelőt, valamint Diels-Alder adduktot tartalmazó… (more)

Subjects/Keywords: poliuretán; Diels-Alder

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APA (6th Edition):

Makrai, A. (n.d.). Diels-Alder adduktot tartalmazó poliuretánok előállítása és vizsgálata . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/239857

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Makrai, Andrea. “Diels-Alder adduktot tartalmazó poliuretánok előállítása és vizsgálata .” Thesis, University of Debrecen. Accessed February 27, 2021. http://hdl.handle.net/2437/239857.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Makrai, Andrea. “Diels-Alder adduktot tartalmazó poliuretánok előállítása és vizsgálata .” Web. 27 Feb 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Makrai A. Diels-Alder adduktot tartalmazó poliuretánok előállítása és vizsgálata . [Internet] [Thesis]. University of Debrecen; [cited 2021 Feb 27]. Available from: http://hdl.handle.net/2437/239857.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Makrai A. Diels-Alder adduktot tartalmazó poliuretánok előállítása és vizsgálata . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/239857

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Boston College

19. 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 February 27, 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. 27 Feb 2021.

Vancouver:

Fort EH. Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems. [Internet] [Doctoral dissertation]. Boston College; 2010. [cited 2021 Feb 27]. 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 Manchester

20. Willis, Mark David. Towards the total synthesis of chaetochalasin A.

Degree: PhD, 2012, University of Manchester

 This thesis describes tin and non-tin mediated approaches towards the total synthesis of chaetochalasin A 1 through an intramolecular domino Diels-Alder approach, and subsequent synthesis… (more)

Subjects/Keywords: 660; Diels-Alder; Natural Product Synthesis

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APA (6th Edition):

Willis, M. D. (2012). Towards the total synthesis of chaetochalasin A. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/towards-the-total-synthesis-of-chaetochalasin-a(07be20b4-6083-42d3-b0f5-c50088d99e5d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564345

Chicago Manual of Style (16th Edition):

Willis, Mark David. “Towards the total synthesis of chaetochalasin A.” 2012. Doctoral Dissertation, University of Manchester. Accessed February 27, 2021. https://www.research.manchester.ac.uk/portal/en/theses/towards-the-total-synthesis-of-chaetochalasin-a(07be20b4-6083-42d3-b0f5-c50088d99e5d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564345.

MLA Handbook (7th Edition):

Willis, Mark David. “Towards the total synthesis of chaetochalasin A.” 2012. Web. 27 Feb 2021.

Vancouver:

Willis MD. Towards the total synthesis of chaetochalasin A. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2021 Feb 27]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/towards-the-total-synthesis-of-chaetochalasin-a(07be20b4-6083-42d3-b0f5-c50088d99e5d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564345.

Council of Science Editors:

Willis MD. Towards the total synthesis of chaetochalasin A. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/towards-the-total-synthesis-of-chaetochalasin-a(07be20b4-6083-42d3-b0f5-c50088d99e5d).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.564345


University of Victoria

21. 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 February 27, 2021. 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. 27 Feb 2021.

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 2021 Feb 27]. 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

22. 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 February 27, 2021. 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. 27 Feb 2021.

Vancouver:

Boloor AG. Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol. [Internet] [Masters thesis]. Montana State University; 1998. [cited 2021 Feb 27]. 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


University of Notre Dame

23. George P Nora. The Synthesis and In Vitro Testing Of Structurally Novel Isoxazolidine Antibacterial Agents Via an Acylnitroso Diels-Alder Reaction</h1>.

Degree: Chemistry and Biochemistry, 2007, University of Notre Dame

  The research in this dissertation focuses on the synthesis and in vitro testing of structurally novel antibacterial agents derived from acylnitroso Diels Alder adducts.… (more)

Subjects/Keywords: acylnitoso diels-alder

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APA (6th Edition):

Nora, G. P. (2007). The Synthesis and In Vitro Testing Of Structurally Novel Isoxazolidine Antibacterial Agents Via an Acylnitroso Diels-Alder Reaction</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/b8515m62t1x

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):

Nora, George P. “The Synthesis and In Vitro Testing Of Structurally Novel Isoxazolidine Antibacterial Agents Via an Acylnitroso Diels-Alder Reaction</h1>.” 2007. Thesis, University of Notre Dame. Accessed February 27, 2021. https://curate.nd.edu/show/b8515m62t1x.

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

MLA Handbook (7th Edition):

Nora, George P. “The Synthesis and In Vitro Testing Of Structurally Novel Isoxazolidine Antibacterial Agents Via an Acylnitroso Diels-Alder Reaction</h1>.” 2007. Web. 27 Feb 2021.

Vancouver:

Nora GP. The Synthesis and In Vitro Testing Of Structurally Novel Isoxazolidine Antibacterial Agents Via an Acylnitroso Diels-Alder Reaction</h1>. [Internet] [Thesis]. University of Notre Dame; 2007. [cited 2021 Feb 27]. Available from: https://curate.nd.edu/show/b8515m62t1x.

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

Council of Science Editors:

Nora GP. The Synthesis and In Vitro Testing Of Structurally Novel Isoxazolidine Antibacterial Agents Via an Acylnitroso Diels-Alder Reaction</h1>. [Thesis]. University of Notre Dame; 2007. Available from: https://curate.nd.edu/show/b8515m62t1x

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


University of Minnesota

24. Emond, Susanna Jean. A synthesis of the octalin core of integramycin, isolation of alkaloids from Amazonian plants, and polyols from renewable resources.

Degree: PhD, Chemistry, 2012, University of Minnesota

 This document is a presentation and discussion on three projects in three parts. Part One is a detailed summary of organic chemistry efforts in the… (more)

Subjects/Keywords: Diels-Alder; Integramycin; Soybean oil; Tabernaemontana; Terpenoids

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

APA (6th Edition):

Emond, S. J. (2012). A synthesis of the octalin core of integramycin, isolation of alkaloids from Amazonian plants, and polyols from renewable resources. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/165308

Chicago Manual of Style (16th Edition):

Emond, Susanna Jean. “A synthesis of the octalin core of integramycin, isolation of alkaloids from Amazonian plants, and polyols from renewable resources.” 2012. Doctoral Dissertation, University of Minnesota. Accessed February 27, 2021. http://hdl.handle.net/11299/165308.

MLA Handbook (7th Edition):

Emond, Susanna Jean. “A synthesis of the octalin core of integramycin, isolation of alkaloids from Amazonian plants, and polyols from renewable resources.” 2012. Web. 27 Feb 2021.

Vancouver:

Emond SJ. A synthesis of the octalin core of integramycin, isolation of alkaloids from Amazonian plants, and polyols from renewable resources. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/11299/165308.

Council of Science Editors:

Emond SJ. A synthesis of the octalin core of integramycin, isolation of alkaloids from Amazonian plants, and polyols from renewable resources. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://hdl.handle.net/11299/165308


University of Minnesota

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

Degree: PhD, Chemistry, 2019, University of Minnesota

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Xiao, Xiao. “The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics.” 2019. Doctoral Dissertation, University of Minnesota. Accessed February 27, 2021. http://hdl.handle.net/11299/206228.

MLA Handbook (7th Edition):

Xiao, Xiao. “The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics.” 2019. Web. 27 Feb 2021.

Vancouver:

Xiao X. The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/11299/206228.

Council of Science Editors:

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


University of Minnesota

26. Woods, Brian Patrick. Spontaneity to serendipity: from an enediyne core biosynthetic hypothesis to the hexadehydro-Diels-Alder reaction.

Degree: PhD, Chemistry, 2014, University of Minnesota

 Enediyne containing natural products have promising potential as cancer therapeutics due to their unique molecular architecture. The (Z)-1,5-diyn-3-ene subunit in the enediyne core can undergo… (more)

Subjects/Keywords: Diels-Alder; Enediyne; HDDA; Methodology; Synthesis; Chemistry

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APA (6th Edition):

Woods, B. P. (2014). Spontaneity to serendipity: from an enediyne core biosynthetic hypothesis to the hexadehydro-Diels-Alder reaction. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/167687

Chicago Manual of Style (16th Edition):

Woods, Brian Patrick. “Spontaneity to serendipity: from an enediyne core biosynthetic hypothesis to the hexadehydro-Diels-Alder reaction.” 2014. Doctoral Dissertation, University of Minnesota. Accessed February 27, 2021. http://hdl.handle.net/11299/167687.

MLA Handbook (7th Edition):

Woods, Brian Patrick. “Spontaneity to serendipity: from an enediyne core biosynthetic hypothesis to the hexadehydro-Diels-Alder reaction.” 2014. Web. 27 Feb 2021.

Vancouver:

Woods BP. Spontaneity to serendipity: from an enediyne core biosynthetic hypothesis to the hexadehydro-Diels-Alder reaction. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/11299/167687.

Council of Science Editors:

Woods BP. Spontaneity to serendipity: from an enediyne core biosynthetic hypothesis to the hexadehydro-Diels-Alder reaction. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/167687


University of Arizona

27. Korth, Bryan David. The Preparation and Modification of Phthalocyanine Containing Materials .

Degree: 2012, University of Arizona

 Phthalocyanines (Pcs) are highly conjugated, 18π-electron cyclic molecules composed of four isoindoline units that exhibit unique optical, electrical and chemical properties. While originally used as… (more)

Subjects/Keywords: Polymer; ROMP; Chemistry; Diels-Alder; Phthalocyanine

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

APA (6th Edition):

Korth, B. D. (2012). The Preparation and Modification of Phthalocyanine Containing Materials . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/228477

Chicago Manual of Style (16th Edition):

Korth, Bryan David. “The Preparation and Modification of Phthalocyanine Containing Materials .” 2012. Doctoral Dissertation, University of Arizona. Accessed February 27, 2021. http://hdl.handle.net/10150/228477.

MLA Handbook (7th Edition):

Korth, Bryan David. “The Preparation and Modification of Phthalocyanine Containing Materials .” 2012. Web. 27 Feb 2021.

Vancouver:

Korth BD. The Preparation and Modification of Phthalocyanine Containing Materials . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/10150/228477.

Council of Science Editors:

Korth BD. The Preparation and Modification of Phthalocyanine Containing Materials . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/228477


Universidad Andrés Bello

28. Vásquez Contreras, Rodrigo Andrés. Síntesis de un aducto diels-alder conjugado a nanopartículas de oro como potencial transportador y liberador de biomoléculas .

Degree: 2014, Universidad Andrés Bello

 Las nanopartículas, dado su tamaño, son especies que tienen la capacidad de penetrar en células de una manera eficiente por lo que son muy útiles… (more)

Subjects/Keywords: Nanopartículas; Reacción de Diels-Alder; Biomoléculas

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

APA (6th Edition):

Vásquez Contreras, R. A. (2014). Síntesis de un aducto diels-alder conjugado a nanopartículas de oro como potencial transportador y liberador de biomoléculas . (Thesis). Universidad Andrés Bello. Retrieved from http://repositorio.unab.cl/xmlui/handle/ria/3771

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):

Vásquez Contreras, Rodrigo Andrés. “Síntesis de un aducto diels-alder conjugado a nanopartículas de oro como potencial transportador y liberador de biomoléculas .” 2014. Thesis, Universidad Andrés Bello. Accessed February 27, 2021. http://repositorio.unab.cl/xmlui/handle/ria/3771.

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

MLA Handbook (7th Edition):

Vásquez Contreras, Rodrigo Andrés. “Síntesis de un aducto diels-alder conjugado a nanopartículas de oro como potencial transportador y liberador de biomoléculas .” 2014. Web. 27 Feb 2021.

Vancouver:

Vásquez Contreras RA. Síntesis de un aducto diels-alder conjugado a nanopartículas de oro como potencial transportador y liberador de biomoléculas . [Internet] [Thesis]. Universidad Andrés Bello; 2014. [cited 2021 Feb 27]. Available from: http://repositorio.unab.cl/xmlui/handle/ria/3771.

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

Council of Science Editors:

Vásquez Contreras RA. Síntesis de un aducto diels-alder conjugado a nanopartículas de oro como potencial transportador y liberador de biomoléculas . [Thesis]. Universidad Andrés Bello; 2014. Available from: http://repositorio.unab.cl/xmlui/handle/ria/3771

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


University of New South Wales

29. Nash, Justin. Application of the Diels-Alder reaction towards the total synthesis of embellistatin and natural product Inspired libraries.

Degree: Chemistry, 2013, University of New South Wales

 Natural products are useful in the drug discovery paradigm, both as drugs and as inspiration for new scaffolds. This thesis is concerned with the synthetic… (more)

Subjects/Keywords: Diels-Alder; Total Synthesis; Natural Products

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

APA (6th Edition):

Nash, J. (2013). Application of the Diels-Alder reaction towards the total synthesis of embellistatin and natural product Inspired libraries. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53178 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11871/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Nash, Justin. “Application of the Diels-Alder reaction towards the total synthesis of embellistatin and natural product Inspired libraries.” 2013. Doctoral Dissertation, University of New South Wales. Accessed February 27, 2021. http://handle.unsw.edu.au/1959.4/53178 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11871/SOURCE02?view=true.

MLA Handbook (7th Edition):

Nash, Justin. “Application of the Diels-Alder reaction towards the total synthesis of embellistatin and natural product Inspired libraries.” 2013. Web. 27 Feb 2021.

Vancouver:

Nash J. Application of the Diels-Alder reaction towards the total synthesis of embellistatin and natural product Inspired libraries. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2021 Feb 27]. Available from: http://handle.unsw.edu.au/1959.4/53178 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11871/SOURCE02?view=true.

Council of Science Editors:

Nash J. Application of the Diels-Alder reaction towards the total synthesis of embellistatin and natural product Inspired libraries. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/53178 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11871/SOURCE02?view=true

30. Horton, Jade A. Exploring Enantioselective and Multicomponent One-Pot Reactions Utilizing Alkynes as Linchpins Toward Biologically Active Molecules.

Degree: 2018, University of Nevada – Reno

 Robust synthetic methodology to make complex small molecules that are of biological importance is a highly investigated area. Utilizing fundamental bond-making reactions, like the Diels-Alder(more)

Subjects/Keywords: Cis-decalin; Diels-Alder; Enantioselective; Polycyclic; Ynones

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

APA (6th Edition):

Horton, J. A. (2018). Exploring Enantioselective and Multicomponent One-Pot Reactions Utilizing Alkynes as Linchpins Toward Biologically Active Molecules. (Thesis). University of Nevada – Reno. Retrieved from http://hdl.handle.net/11714/4857

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):

Horton, Jade A. “Exploring Enantioselective and Multicomponent One-Pot Reactions Utilizing Alkynes as Linchpins Toward Biologically Active Molecules.” 2018. Thesis, University of Nevada – Reno. Accessed February 27, 2021. http://hdl.handle.net/11714/4857.

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

MLA Handbook (7th Edition):

Horton, Jade A. “Exploring Enantioselective and Multicomponent One-Pot Reactions Utilizing Alkynes as Linchpins Toward Biologically Active Molecules.” 2018. Web. 27 Feb 2021.

Vancouver:

Horton JA. Exploring Enantioselective and Multicomponent One-Pot Reactions Utilizing Alkynes as Linchpins Toward Biologically Active Molecules. [Internet] [Thesis]. University of Nevada – Reno; 2018. [cited 2021 Feb 27]. Available from: http://hdl.handle.net/11714/4857.

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

Council of Science Editors:

Horton JA. Exploring Enantioselective and Multicomponent One-Pot Reactions Utilizing Alkynes as Linchpins Toward Biologically Active Molecules. [Thesis]. University of Nevada – Reno; 2018. Available from: http://hdl.handle.net/11714/4857

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

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