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You searched for subject:(Diels Alder). Showing records 1 – 30 of 403 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 September 22, 2019. http://hdl.handle.net/11343/36621.

MLA Handbook (7th Edition):

GUNAWAN, CHRISTIAN. “Studies towards the synthesis of mulberry Diels-Alder adducts.” 2011. Web. 22 Sep 2019.

Vancouver:

GUNAWAN C. Studies towards the synthesis of mulberry Diels-Alder adducts. [Internet] [Doctoral dissertation]. University of Melbourne; 2011. [cited 2019 Sep 22]. 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 September 22, 2019. 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. 22 Sep 2019.

Vancouver:

Schwartz JP. Expanding the scope of a Diels-Alder approach to biaryl synthesis. [Internet] [Doctoral dissertation]. Oregon State University; 2009. [cited 2019 Sep 22]. 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 September 22, 2019. 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. 22 Sep 2019.

Vancouver:

Levandowski B. Diels-Alder Reactivities of Cyclic Dienes and Dienophiles. [Internet] [Thesis]. UCLA; 2018. [cited 2019 Sep 22]. 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


Australian National University

4. Tan, Siu Min. Multicomponent Diels-Alder Sequences of 1-Aminodendralenes .

Degree: 2017, Australian National University

 This thesis explores the use of in situ generated acyclic 1-aminodendralenes in multicomponent diene-transmissive Diels-Alder (DTDA) reaction sequences. Dendralenes have previously been shown to generate… (more)

Subjects/Keywords: Diels-Alder; aminodendralene; multicomponent reaction

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APA (6th Edition):

Tan, S. M. (2017). Multicomponent Diels-Alder Sequences of 1-Aminodendralenes . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/143040

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):

Tan, Siu Min. “Multicomponent Diels-Alder Sequences of 1-Aminodendralenes .” 2017. Thesis, Australian National University. Accessed September 22, 2019. http://hdl.handle.net/1885/143040.

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

MLA Handbook (7th Edition):

Tan, Siu Min. “Multicomponent Diels-Alder Sequences of 1-Aminodendralenes .” 2017. Web. 22 Sep 2019.

Vancouver:

Tan SM. Multicomponent Diels-Alder Sequences of 1-Aminodendralenes . [Internet] [Thesis]. Australian National University; 2017. [cited 2019 Sep 22]. Available from: http://hdl.handle.net/1885/143040.

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

Council of Science Editors:

Tan SM. Multicomponent Diels-Alder Sequences of 1-Aminodendralenes . [Thesis]. Australian National University; 2017. Available from: http://hdl.handle.net/1885/143040

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


University of New South Wales

5. 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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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


University of Guelph

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

Degree: 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 . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3561

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):

Nikoloska, Irena. “Towards the Synthesis of Novel PARP Inhibitors through Diels-Alder Chemistry .” 2012. Thesis, University of Guelph. Accessed September 22, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3561.

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

MLA Handbook (7th Edition):

Nikoloska, Irena. “Towards the Synthesis of Novel PARP Inhibitors through Diels-Alder Chemistry .” 2012. Web. 22 Sep 2019.

Vancouver:

Nikoloska I. Towards the Synthesis of Novel PARP Inhibitors through Diels-Alder Chemistry . [Internet] [Thesis]. University of Guelph; 2012. [cited 2019 Sep 22]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3561.

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

Council of Science Editors:

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

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


University of Guelph

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

Degree: 2018, University of Guelph

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Petko, Dina. “Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition .” 2018. Thesis, University of Guelph. Accessed September 22, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094.

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

MLA Handbook (7th Edition):

Petko, Dina. “Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition .” 2018. Web. 22 Sep 2019.

Vancouver:

Petko D. Ruthenium Catalyzed Bis-Homo-Diels-Alder [2+2+2] Cycloaddition . [Internet] [Thesis]. University of Guelph; 2018. [cited 2019 Sep 22]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/14094.

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

Council of Science Editors:

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

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

8. 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 September 22, 2019. 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. 22 Sep 2019.

Vancouver:

Barbosa JdS. Estudo sobre a síntese de furanoliangolidos pela Reação de Diels-Alder. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2019 Sep 22]. 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/ ;


University of Minnesota

9. Lanzatella, Nicholas Peter. Access to Indoles via Diels-Alder reactions of vinylpyrroles.

Degree: PhD, Chemistry, 2009, University of Minnesota

 The indole moiety is extremely common in biologically active natural and un-natural products. Exploration and discovery of methods for generating the indole nucleus provides new… (more)

Subjects/Keywords: Diels-Alder; Diels-Alder Dimer; Indole; Tetrahydroindole; Vinylboronate; Vinylpyrrole; Chemistry

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APA (6th Edition):

Lanzatella, N. P. (2009). Access to Indoles via Diels-Alder reactions of vinylpyrroles. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/56304

Chicago Manual of Style (16th Edition):

Lanzatella, Nicholas Peter. “Access to Indoles via Diels-Alder reactions of vinylpyrroles.” 2009. Doctoral Dissertation, University of Minnesota. Accessed September 22, 2019. http://purl.umn.edu/56304.

MLA Handbook (7th Edition):

Lanzatella, Nicholas Peter. “Access to Indoles via Diels-Alder reactions of vinylpyrroles.” 2009. Web. 22 Sep 2019.

Vancouver:

Lanzatella NP. Access to Indoles via Diels-Alder reactions of vinylpyrroles. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2019 Sep 22]. Available from: http://purl.umn.edu/56304.

Council of Science Editors:

Lanzatella NP. Access to Indoles via Diels-Alder reactions of vinylpyrroles. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/56304

10. 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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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


Universidade do Rio Grande do Norte

11. 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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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

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

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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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

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

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 September 22, 2019. 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. 22 Sep 2019.

Vancouver:

Donatoni MC. A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas. [Internet] [Thesis]. Universidade Federal de São Carlos; 2008. [cited 2019 Sep 22]. 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


Wright State University

14. VanNess, Brandon G. Synthetic approach to epibatidine from 1-(phenylsulfonyl)pyrrole.

Degree: MS, Chemistry, 2007, Wright State University

 The goal of this research was to synthesize the natural product epibatidine, a non-opiate analgesic and nicotinic acetylcholine agonist isolated from <i>Epipedobates tricolor</i>. A synthetic… (more)

Subjects/Keywords: Chemistry, Organic; epibatidine; Diels-Alder; pyrrole

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

APA (6th Edition):

VanNess, B. G. (2007). Synthetic approach to epibatidine from 1-(phenylsulfonyl)pyrrole. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1183494979

Chicago Manual of Style (16th Edition):

VanNess, Brandon G. “Synthetic approach to epibatidine from 1-(phenylsulfonyl)pyrrole.” 2007. Masters Thesis, Wright State University. Accessed September 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1183494979.

MLA Handbook (7th Edition):

VanNess, Brandon G. “Synthetic approach to epibatidine from 1-(phenylsulfonyl)pyrrole.” 2007. Web. 22 Sep 2019.

Vancouver:

VanNess BG. Synthetic approach to epibatidine from 1-(phenylsulfonyl)pyrrole. [Internet] [Masters thesis]. Wright State University; 2007. [cited 2019 Sep 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1183494979.

Council of Science Editors:

VanNess BG. Synthetic approach to epibatidine from 1-(phenylsulfonyl)pyrrole. [Masters Thesis]. Wright State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1183494979


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 September 22, 2019. 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. 22 Sep 2019.

Vancouver:

Dei Rossi DR. The use of the Diels-Alder reaction in asymmetric synthesis. [Internet] [Masters thesis]. Oregon State University; 1978. [cited 2019 Sep 22]. 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


Universidad Andrés Bello

16. 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 (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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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 Manchester

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

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 September 22, 2019. 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. 22 Sep 2019.

Vancouver:

Willis MD. Towards the total synthesis of chaetochalasin A. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2019 Sep 22]. 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


UCLA

18. 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 September 22, 2019. 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. 22 Sep 2019.

Vancouver:

LIU F. Theory of gated hemicarcerands and Diels-Alder reactions of tetrazines. [Internet] [Thesis]. UCLA; 2014. [cited 2019 Sep 22]. 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


Montana State University

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

Degree: 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. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/8541

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):

Boloor, Amogh G. “Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol.” 1998. Thesis, Montana State University. Accessed September 22, 2019. https://scholarworks.montana.edu/xmlui/handle/1/8541.

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

MLA Handbook (7th Edition):

Boloor, Amogh G. “Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol.” 1998. Web. 22 Sep 2019.

Vancouver:

Boloor AG. Progress towards intramolecular Diels-Alder model study towards (+-) polyandrol. [Internet] [Thesis]. Montana State University; 1998. [cited 2019 Sep 22]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/8541.

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

Council of Science Editors:

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

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


University of Victoria

20. 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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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


Drexel University

21. 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 September 22, 2019. 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. 22 Sep 2019.

Vancouver:

Peterson AM. Development of remendable polymer composites using a thermoreversible reaction. [Internet] [Thesis]. Drexel University; 2011. [cited 2019 Sep 22]. 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 Debrecen

22. 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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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.


University of New South Wales

23. 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 (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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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


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 (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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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. 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 September 22, 2019. 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. 22 Sep 2019.

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 2019 Sep 22]. 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


Boston College

26. 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 September 22, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101647.

MLA Handbook (7th Edition):

Fort, Eric Henry. “Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems.” 2010. Web. 22 Sep 2019.

Vancouver:

Fort EH. Developing Methods for Growing Single-Chirality Carbon Nanotubes and Other Aromatic Systems. [Internet] [Doctoral dissertation]. Boston College; 2010. [cited 2019 Sep 22]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101647.

Council of Science Editors:

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


University of Notre Dame

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

Degree: PhD, 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>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/b8515m62t1x

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. Doctoral Dissertation, University of Notre Dame. Accessed September 22, 2019. https://curate.nd.edu/show/b8515m62t1x.

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. 22 Sep 2019.

Vancouver:

Nora GP. The Synthesis and In Vitro Testing Of Structurally Novel Isoxazolidine Antibacterial Agents Via an Acylnitroso Diels-Alder Reaction</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2007. [cited 2019 Sep 22]. Available from: https://curate.nd.edu/show/b8515m62t1x.

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>. [Doctoral Dissertation]. University of Notre Dame; 2007. Available from: https://curate.nd.edu/show/b8515m62t1x


University of Minnesota

28. 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 September 22, 2019. http://hdl.handle.net/11299/206228.

MLA Handbook (7th Edition):

Xiao, Xiao. “The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics.” 2019. Web. 22 Sep 2019.

Vancouver:

Xiao X. The Hexadehydro-Diels–Alder (HDDA) Reaction-Enabled Bottom-up Synthesis of Elaborated Polycyclic Aromatics. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2019 Sep 22]. 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 Arizona

29. 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 (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 September 22, 2019. http://hdl.handle.net/10150/228477.

MLA Handbook (7th Edition):

Korth, Bryan David. “The Preparation and Modification of Phthalocyanine Containing Materials .” 2012. Web. 22 Sep 2019.

Vancouver:

Korth BD. The Preparation and Modification of Phthalocyanine Containing Materials . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2019 Sep 22]. 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


University of Arizona

30. Smith, Brandon Robert. Oxidative Dearomatization / Diels-Alder Approaches to Maoecrystal V and the Gibberellin Family of Natural Products .

Degree: 2018, University of Arizona

 Synthetic approaches to the complex natural product maoecrystal V and the gibberellin family of natural products are presented. The two approaches are united by an… (more)

Subjects/Keywords: Diels Alder; gibberellin; maoecrystal V; total synthesis

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APA (6th Edition):

Smith, B. R. (2018). Oxidative Dearomatization / Diels-Alder Approaches to Maoecrystal V and the Gibberellin Family of Natural Products . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/628183

Chicago Manual of Style (16th Edition):

Smith, Brandon Robert. “Oxidative Dearomatization / Diels-Alder Approaches to Maoecrystal V and the Gibberellin Family of Natural Products .” 2018. Doctoral Dissertation, University of Arizona. Accessed September 22, 2019. http://hdl.handle.net/10150/628183.

MLA Handbook (7th Edition):

Smith, Brandon Robert. “Oxidative Dearomatization / Diels-Alder Approaches to Maoecrystal V and the Gibberellin Family of Natural Products .” 2018. Web. 22 Sep 2019.

Vancouver:

Smith BR. Oxidative Dearomatization / Diels-Alder Approaches to Maoecrystal V and the Gibberellin Family of Natural Products . [Internet] [Doctoral dissertation]. University of Arizona; 2018. [cited 2019 Sep 22]. Available from: http://hdl.handle.net/10150/628183.

Council of Science Editors:

Smith BR. Oxidative Dearomatization / Diels-Alder Approaches to Maoecrystal V and the Gibberellin Family of Natural Products . [Doctoral Dissertation]. University of Arizona; 2018. Available from: http://hdl.handle.net/10150/628183

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