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You searched for subject:(multicomponent reactions). Showing records 1 – 30 of 51 total matches.

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Punjabi University

1. Suresh. Synthetic study in pyrimidines and related heterocyclics and new synthetic methods; -.

Degree: Chemistry, 2011, Punjabi University

The thesis entitled ?Synthetic study in pyrimidines and related heterocyclics and new synthetic methods?, is structured like this, as the title indicates it is in… (more)

Subjects/Keywords: Multicomponent Reactions; Uracils; Chemistry

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APA (6th Edition):

Suresh. (2011). Synthetic study in pyrimidines and related heterocyclics and new synthetic methods; -. (Thesis). Punjabi University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/4928

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

Chicago Manual of Style (16th Edition):

Suresh. “Synthetic study in pyrimidines and related heterocyclics and new synthetic methods; -.” 2011. Thesis, Punjabi University. Accessed October 23, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/4928.

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

MLA Handbook (7th Edition):

Suresh. “Synthetic study in pyrimidines and related heterocyclics and new synthetic methods; -.” 2011. Web. 23 Oct 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Suresh. Synthetic study in pyrimidines and related heterocyclics and new synthetic methods; -. [Internet] [Thesis]. Punjabi University; 2011. [cited 2019 Oct 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4928.

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

Council of Science Editors:

Suresh. Synthetic study in pyrimidines and related heterocyclics and new synthetic methods; -. [Thesis]. Punjabi University; 2011. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4928

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


Miami University

2. Deng, Yongming. Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins.

Degree: PhD, Chemistry, 2014, Miami University

 The combination of enamine catalysis with metal catalysis, aiming to achieve organic transformations that cannot be accessed by enamine catalysis or metal catalysis independently, promises… (more)

Subjects/Keywords: Chemistry; cooperative catalysis; enamines; Lewis acids; multicomponent reactions; aza-Diels-Alder reactions

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APA (6th Edition):

Deng, Y. (2014). Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins. (Doctoral Dissertation). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1406213121

Chicago Manual of Style (16th Edition):

Deng, Yongming. “Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins.” 2014. Doctoral Dissertation, Miami University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=miami1406213121.

MLA Handbook (7th Edition):

Deng, Yongming. “Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins.” 2014. Web. 23 Oct 2019.

Vancouver:

Deng Y. Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins. [Internet] [Doctoral dissertation]. Miami University; 2014. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1406213121.

Council of Science Editors:

Deng Y. Asymmetric cyclization reactions through an enamine/acid cooperative approach. Synthesis of unsymmetrically functionalized benzoporphyrins. [Doctoral Dissertation]. Miami University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1406213121

3. Kale, Sandip Ravindra. Multicomponent reactions catalyzed by Hydrotalcites and Hydroxyapatites; -.

Degree: Chemistry, 2013, INFLIBNET

None

References p. 255-280

Advisors/Committee Members: Jayaram, Radha V.

Subjects/Keywords: Chemistry; Catalysis; Multicomponent Reactions

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APA (6th Edition):

Kale, S. R. (2013). Multicomponent reactions catalyzed by Hydrotalcites and Hydroxyapatites; -. (Thesis). INFLIBNET. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/12353

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):

Kale, Sandip Ravindra. “Multicomponent reactions catalyzed by Hydrotalcites and Hydroxyapatites; -.” 2013. Thesis, INFLIBNET. Accessed October 23, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/12353.

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

MLA Handbook (7th Edition):

Kale, Sandip Ravindra. “Multicomponent reactions catalyzed by Hydrotalcites and Hydroxyapatites; -.” 2013. Web. 23 Oct 2019.

Vancouver:

Kale SR. Multicomponent reactions catalyzed by Hydrotalcites and Hydroxyapatites; -. [Internet] [Thesis]. INFLIBNET; 2013. [cited 2019 Oct 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12353.

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

Council of Science Editors:

Kale SR. Multicomponent reactions catalyzed by Hydrotalcites and Hydroxyapatites; -. [Thesis]. INFLIBNET; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/12353

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


University of Southern California

4. Myslinska, Malgorzata. New organoboron based multicomponent methodologies for the synthesis of novel heterocycles.

Degree: PhD, Chemistry, 2011, University of Southern California

 This dissertation describes the development of new, efficient and facile synthetic methodologies for the practical synthesis of novel heterocycles and highly substituted amine derivatives.; Chapter… (more)

Subjects/Keywords: multicomponent reactions; indole synthesis; Petasis reaction; propargylamines; organotrifluoroborates

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APA (6th Edition):

Myslinska, M. (2011). New organoboron based multicomponent methodologies for the synthesis of novel heterocycles. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/277397/rec/4397

Chicago Manual of Style (16th Edition):

Myslinska, Malgorzata. “New organoboron based multicomponent methodologies for the synthesis of novel heterocycles.” 2011. Doctoral Dissertation, University of Southern California. Accessed October 23, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/277397/rec/4397.

MLA Handbook (7th Edition):

Myslinska, Malgorzata. “New organoboron based multicomponent methodologies for the synthesis of novel heterocycles.” 2011. Web. 23 Oct 2019.

Vancouver:

Myslinska M. New organoboron based multicomponent methodologies for the synthesis of novel heterocycles. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2019 Oct 23]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/277397/rec/4397.

Council of Science Editors:

Myslinska M. New organoboron based multicomponent methodologies for the synthesis of novel heterocycles. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/277397/rec/4397


Vrije Universiteit Amsterdam

5. Mooijman, M. C2-functionalized 2-imidazolidines and 2-imidazolines Multicomponent Synthesis and Synthetic Potential .

Degree: 2012, Vrije Universiteit Amsterdam

Subjects/Keywords: Organic Chemistry; Synthesis; Multicomponent Reactions

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APA (6th Edition):

Mooijman, M. (2012). C2-functionalized 2-imidazolidines and 2-imidazolines Multicomponent Synthesis and Synthetic Potential . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/39358

Chicago Manual of Style (16th Edition):

Mooijman, M. “C2-functionalized 2-imidazolidines and 2-imidazolines Multicomponent Synthesis and Synthetic Potential .” 2012. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 23, 2019. http://hdl.handle.net/1871/39358.

MLA Handbook (7th Edition):

Mooijman, M. “C2-functionalized 2-imidazolidines and 2-imidazolines Multicomponent Synthesis and Synthetic Potential .” 2012. Web. 23 Oct 2019.

Vancouver:

Mooijman M. C2-functionalized 2-imidazolidines and 2-imidazolines Multicomponent Synthesis and Synthetic Potential . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2012. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1871/39358.

Council of Science Editors:

Mooijman M. C2-functionalized 2-imidazolidines and 2-imidazolines Multicomponent Synthesis and Synthetic Potential . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2012. Available from: http://hdl.handle.net/1871/39358


Boston College

6. Cho, Hee Yeon. Catalytic Borylative Multicomponent Coupling Reactions and Novel Chemistry of Polycyclic Aromatic Hydrocarbons.

Degree: PhD, Chemistry, 2013, Boston College

 Expeditious establishment of molecular complexity in a stereoselective manner is a prominent goal in organic synthesis. In this regard, multicomponent coupling reactions have received substantial… (more)

Subjects/Keywords: Catalysis; Multicomponent Reactions; Organic Materials; Organometallics; Polycyclic Aromatic Hydrocarbons

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APA (6th Edition):

Cho, H. Y. (2013). Catalytic Borylative Multicomponent Coupling Reactions and Novel Chemistry of Polycyclic Aromatic Hydrocarbons. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101765

Chicago Manual of Style (16th Edition):

Cho, Hee Yeon. “Catalytic Borylative Multicomponent Coupling Reactions and Novel Chemistry of Polycyclic Aromatic Hydrocarbons.” 2013. Doctoral Dissertation, Boston College. Accessed October 23, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101765.

MLA Handbook (7th Edition):

Cho, Hee Yeon. “Catalytic Borylative Multicomponent Coupling Reactions and Novel Chemistry of Polycyclic Aromatic Hydrocarbons.” 2013. Web. 23 Oct 2019.

Vancouver:

Cho HY. Catalytic Borylative Multicomponent Coupling Reactions and Novel Chemistry of Polycyclic Aromatic Hydrocarbons. [Internet] [Doctoral dissertation]. Boston College; 2013. [cited 2019 Oct 23]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101765.

Council of Science Editors:

Cho HY. Catalytic Borylative Multicomponent Coupling Reactions and Novel Chemistry of Polycyclic Aromatic Hydrocarbons. [Doctoral Dissertation]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101765


University of Southern California

7. Bychinskaya, Inessa. Multicomponent reactions for the synthesis of fluorinated organic compounds and related chemistry.

Degree: PhD, Chemistry, 2011, University of Southern California

 Development of eco- and aqueous friendly, stable and recyclable catalysts for organic synthesis is one of the major steps in safe, environmentally benign and sustainable… (more)

Subjects/Keywords: bening catalysis; biologically active compounds; multicomponent reactions; organofluorine compounds

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APA (6th Edition):

Bychinskaya, I. (2011). Multicomponent reactions for the synthesis of fluorinated organic compounds and related chemistry. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/668337/rec/4256

Chicago Manual of Style (16th Edition):

Bychinskaya, Inessa. “Multicomponent reactions for the synthesis of fluorinated organic compounds and related chemistry.” 2011. Doctoral Dissertation, University of Southern California. Accessed October 23, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/668337/rec/4256.

MLA Handbook (7th Edition):

Bychinskaya, Inessa. “Multicomponent reactions for the synthesis of fluorinated organic compounds and related chemistry.” 2011. Web. 23 Oct 2019.

Vancouver:

Bychinskaya I. Multicomponent reactions for the synthesis of fluorinated organic compounds and related chemistry. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2019 Oct 23]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/668337/rec/4256.

Council of Science Editors:

Bychinskaya I. Multicomponent reactions for the synthesis of fluorinated organic compounds and related chemistry. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/668337/rec/4256


Vrije Universiteit Amsterdam

8. Groenendaal, B. Multicomponent Reactions .

Degree: 2009, Vrije Universiteit Amsterdam

Subjects/Keywords: Multicomponent reactions: studies toward scaffold and stereochemical diversity; Multicomponent Reactions; Biocatalysis; Bas Groenendaal

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APA (6th Edition):

Groenendaal, B. (2009). Multicomponent Reactions . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/16301

Chicago Manual of Style (16th Edition):

Groenendaal, B. “Multicomponent Reactions .” 2009. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 23, 2019. http://hdl.handle.net/1871/16301.

MLA Handbook (7th Edition):

Groenendaal, B. “Multicomponent Reactions .” 2009. Web. 23 Oct 2019.

Vancouver:

Groenendaal B. Multicomponent Reactions . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2009. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1871/16301.

Council of Science Editors:

Groenendaal B. Multicomponent Reactions . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2009. Available from: http://hdl.handle.net/1871/16301


Universidade Federal de Viçosa

9. Carmindo Ribeiro Borel. Desenvolvimento de reações multicomponentes para a síntese de 2-(2-piridil)quinolinas.

Degree: 2013, Universidade Federal de Viçosa

Estreptonigrina é um antibiótico antitumoral altamente funcionalizado que tem atraído considerável atenção de químicos orgânicos sintéticos e bioquímicos, ambos interessados em suas propriedades peculiares, em… (more)

Subjects/Keywords: Reação multicomponente; Piridilquinolinas; Reações de povarov; QUIMICA ORGANICA; Multicomponent reaction; Piridilquinolinas; Reactions Povarov

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APA (6th Edition):

Borel, C. R. (2013). Desenvolvimento de reações multicomponentes para a síntese de 2-(2-piridil)quinolinas. (Thesis). Universidade Federal de Viçosa. Retrieved from http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=5415

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):

Borel, Carmindo Ribeiro. “Desenvolvimento de reações multicomponentes para a síntese de 2-(2-piridil)quinolinas.” 2013. Thesis, Universidade Federal de Viçosa. Accessed October 23, 2019. http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=5415.

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

MLA Handbook (7th Edition):

Borel, Carmindo Ribeiro. “Desenvolvimento de reações multicomponentes para a síntese de 2-(2-piridil)quinolinas.” 2013. Web. 23 Oct 2019.

Vancouver:

Borel CR. Desenvolvimento de reações multicomponentes para a síntese de 2-(2-piridil)quinolinas. [Internet] [Thesis]. Universidade Federal de Viçosa; 2013. [cited 2019 Oct 23]. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=5415.

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

Council of Science Editors:

Borel CR. Desenvolvimento de reações multicomponentes para a síntese de 2-(2-piridil)quinolinas. [Thesis]. Universidade Federal de Viçosa; 2013. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=5415

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


Queens University

10. Cosman, Jennifer. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .

Degree: Chemistry, 2015, Queens University

 Chapter one of this thesis describes the iridium-catalyzed ortho-selective C–H borylation reaction of tertiary benzamides. An iridium(I) complex paired with an electron-deficient phosphine ligand allows… (more)

Subjects/Keywords: multicomponent reactions; C-H activation; allylic substitution; Mizoroki-Heck reaction; iridium-catalyzed C-H borylation

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APA (6th Edition):

Cosman, J. (2015). Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13534

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):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Thesis, Queens University. Accessed October 23, 2019. http://hdl.handle.net/1974/13534.

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

MLA Handbook (7th Edition):

Cosman, Jennifer. “Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions .” 2015. Web. 23 Oct 2019.

Vancouver:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1974/13534.

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

Council of Science Editors:

Cosman J. Advances in Metal-Catalyzed C–H Borylation and Multicomponent Allylic Substitution Reactions . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13534

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

11. Jia, Shuanglong. Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives : Réactions multicomposantes envers les hétérocycles et la réaction de Tsuji-Trost des dérivés nitrés allyliques.

Degree: Docteur es, Chimie, 2018, Paris Saclay

Les réactions multicomposantes jouent un rôle important en chimie organique. Ce sont des réactions qui mettent en jeu au moins trois réactifs de départ et… (more)

Subjects/Keywords: Réactions à plusieurs composants; Hétérocycles; Hydrazones; Réactions de Tsuji-Trost; Naphtalène; Multicomponent reactions; Heterocycles; Hydrazones; Tsuji-Trost reactions; Naphthalene; 547.2

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APA (6th Edition):

Jia, S. (2018). Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives : Réactions multicomposantes envers les hétérocycles et la réaction de Tsuji-Trost des dérivés nitrés allyliques. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLY012

Chicago Manual of Style (16th Edition):

Jia, Shuanglong. “Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives : Réactions multicomposantes envers les hétérocycles et la réaction de Tsuji-Trost des dérivés nitrés allyliques.” 2018. Doctoral Dissertation, Paris Saclay. Accessed October 23, 2019. http://www.theses.fr/2018SACLY012.

MLA Handbook (7th Edition):

Jia, Shuanglong. “Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives : Réactions multicomposantes envers les hétérocycles et la réaction de Tsuji-Trost des dérivés nitrés allyliques.” 2018. Web. 23 Oct 2019.

Vancouver:

Jia S. Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives : Réactions multicomposantes envers les hétérocycles et la réaction de Tsuji-Trost des dérivés nitrés allyliques. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2018SACLY012.

Council of Science Editors:

Jia S. Multicomponent Reactions toward Heterocycles and Tsuji-Trost Reaction of Allylic Nitro Derivatives : Réactions multicomposantes envers les hétérocycles et la réaction de Tsuji-Trost des dérivés nitrés allyliques. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLY012

12. Carmona, Rafaela Costa. Estratégias assimétricas em reações de acoplamento A3.

Degree: Mestrado, Química, 2013, University of São Paulo

A presente dissertação de mestrado descreve estudos sobre as reações multicomponentes A3 na versão assimétrica. Diversas metodologias foram empregadas visando a obtenção de propargilaminas opticamente… (more)

Subjects/Keywords: A3-coupling reaction; Multicomponent reaction; Organic reactions; Propargilaminas; Propargylamines; Reação de acoplamento A3; Reação multicomponente; Reações orgânica

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APA (6th Edition):

Carmona, R. C. (2013). Estratégias assimétricas em reações de acoplamento A3. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46136/tde-23042013-082023/ ;

Chicago Manual of Style (16th Edition):

Carmona, Rafaela Costa. “Estratégias assimétricas em reações de acoplamento A3.” 2013. Masters Thesis, University of São Paulo. Accessed October 23, 2019. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-23042013-082023/ ;.

MLA Handbook (7th Edition):

Carmona, Rafaela Costa. “Estratégias assimétricas em reações de acoplamento A3.” 2013. Web. 23 Oct 2019.

Vancouver:

Carmona RC. Estratégias assimétricas em reações de acoplamento A3. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2019 Oct 23]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-23042013-082023/ ;.

Council of Science Editors:

Carmona RC. Estratégias assimétricas em reações de acoplamento A3. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-23042013-082023/ ;

13. Vasconcelos, Stanley Nunes Siqueira. Síntese de 5-organoteluro-1H-1,2,3-triazóis-1,4-dissubstituídos, funcionalização via reação de acoplamento cruzado de Sonogashira e síntese one-pot de derivados do indol-3-glioxila e indol-3-glioxil-1,2,3-triazóis.

Degree: Mestrado, Insumos Farmacêuticos, 2013, University of São Paulo

No capítulo 1 apresentamos uma síntese eficiente de compostos 5-organoteluro-1H- 1,2,3-triazóis realizada via reação de cicloadição [3+2] entre azidas orgânicas e alquinos substituídos com organotelúrio.… (more)

Subjects/Keywords: Alkynes; Alquinos; Click Chemistry; Click Chemistry; Indol; Indole; Multicomponent reactions (MCRs); Reações Multicomponente (MCRs); Sonogashira; Sonogashira; Tellurium; Telurio; Triazol; Triazole

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APA (6th Edition):

Vasconcelos, S. N. S. (2013). Síntese de 5-organoteluro-1H-1,2,3-triazóis-1,4-dissubstituídos, funcionalização via reação de acoplamento cruzado de Sonogashira e síntese one-pot de derivados do indol-3-glioxila e indol-3-glioxil-1,2,3-triazóis. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/9/9138/tde-16012014-141941/ ;

Chicago Manual of Style (16th Edition):

Vasconcelos, Stanley Nunes Siqueira. “Síntese de 5-organoteluro-1H-1,2,3-triazóis-1,4-dissubstituídos, funcionalização via reação de acoplamento cruzado de Sonogashira e síntese one-pot de derivados do indol-3-glioxila e indol-3-glioxil-1,2,3-triazóis.” 2013. Masters Thesis, University of São Paulo. Accessed October 23, 2019. http://www.teses.usp.br/teses/disponiveis/9/9138/tde-16012014-141941/ ;.

MLA Handbook (7th Edition):

Vasconcelos, Stanley Nunes Siqueira. “Síntese de 5-organoteluro-1H-1,2,3-triazóis-1,4-dissubstituídos, funcionalização via reação de acoplamento cruzado de Sonogashira e síntese one-pot de derivados do indol-3-glioxila e indol-3-glioxil-1,2,3-triazóis.” 2013. Web. 23 Oct 2019.

Vancouver:

Vasconcelos SNS. Síntese de 5-organoteluro-1H-1,2,3-triazóis-1,4-dissubstituídos, funcionalização via reação de acoplamento cruzado de Sonogashira e síntese one-pot de derivados do indol-3-glioxila e indol-3-glioxil-1,2,3-triazóis. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2019 Oct 23]. Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-16012014-141941/ ;.

Council of Science Editors:

Vasconcelos SNS. Síntese de 5-organoteluro-1H-1,2,3-triazóis-1,4-dissubstituídos, funcionalização via reação de acoplamento cruzado de Sonogashira e síntese one-pot de derivados do indol-3-glioxila e indol-3-glioxil-1,2,3-triazóis. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-16012014-141941/ ;

14. Santos, Luna Schlittler [UNESP]. Sínteses quimioenzimáticas de moléculas bioativas: uma abordagem à química verde.

Degree: 2017, Universidade Estadual Paulista

O emprego da Biocatálise utilizando enzimas isoladas ou células íntegras fornece alternativas eficientes e potencialmente quimio-, regio- e estereosseletivas para a transformação de uma ampla… (more)

Subjects/Keywords: Biocatálise; Síntese assimétrica; Saccharomyces cerevisiae; Compostos heterocíclicos; Química verde; Bioreduction; Morita-Baylis-Hillman adducts; Multicomponent reactions; 4-Thiazolidinones

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

APA (6th Edition):

Santos, L. S. [. (2017). Sínteses quimioenzimáticas de moléculas bioativas: uma abordagem à química verde. (Thesis). Universidade Estadual Paulista. Retrieved from http://hdl.handle.net/11449/151850

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):

Santos, Luna Schlittler [UNESP]. “Sínteses quimioenzimáticas de moléculas bioativas: uma abordagem à química verde.” 2017. Thesis, Universidade Estadual Paulista. Accessed October 23, 2019. http://hdl.handle.net/11449/151850.

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

MLA Handbook (7th Edition):

Santos, Luna Schlittler [UNESP]. “Sínteses quimioenzimáticas de moléculas bioativas: uma abordagem à química verde.” 2017. Web. 23 Oct 2019.

Vancouver:

Santos LS[. Sínteses quimioenzimáticas de moléculas bioativas: uma abordagem à química verde. [Internet] [Thesis]. Universidade Estadual Paulista; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/11449/151850.

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

Council of Science Editors:

Santos LS[. Sínteses quimioenzimáticas de moléculas bioativas: uma abordagem à química verde. [Thesis]. Universidade Estadual Paulista; 2017. Available from: http://hdl.handle.net/11449/151850

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

15. Du, Haiying. Michael addition-initiated organocatalytic enantioselective multicomponent reactions with 1,3-dicarbonyls : Réactions multicomposants organocatalysées enantiosélectives initiées par l'addition de Michael de dérivés 1,3 dicarbonyles.

Degree: Docteur es, Chimie organique, 2014, Ecole centrale de Marseille

Ce mémoire de thèse se concentre sur le développement de réactions multicomposants énantiosélectives de dérivés 1,3-Dicarbonylés en présence d'un organocatalyseur, en vue de préparer des… (more)

Subjects/Keywords: 1,3 dicarbonyles; Enantiosélectivité; Organocatalyse; Réactions multicomposants; Addition de Michael; 1,3 -Dicarbonyls; Enantioselectivity; Organocatalysis; Multicomponent reactions; Michael addition; 540

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APA (6th Edition):

Du, H. (2014). Michael addition-initiated organocatalytic enantioselective multicomponent reactions with 1,3-dicarbonyls : Réactions multicomposants organocatalysées enantiosélectives initiées par l'addition de Michael de dérivés 1,3 dicarbonyles. (Doctoral Dissertation). Ecole centrale de Marseille. Retrieved from http://www.theses.fr/2014ECDM0002

Chicago Manual of Style (16th Edition):

Du, Haiying. “Michael addition-initiated organocatalytic enantioselective multicomponent reactions with 1,3-dicarbonyls : Réactions multicomposants organocatalysées enantiosélectives initiées par l'addition de Michael de dérivés 1,3 dicarbonyles.” 2014. Doctoral Dissertation, Ecole centrale de Marseille. Accessed October 23, 2019. http://www.theses.fr/2014ECDM0002.

MLA Handbook (7th Edition):

Du, Haiying. “Michael addition-initiated organocatalytic enantioselective multicomponent reactions with 1,3-dicarbonyls : Réactions multicomposants organocatalysées enantiosélectives initiées par l'addition de Michael de dérivés 1,3 dicarbonyles.” 2014. Web. 23 Oct 2019.

Vancouver:

Du H. Michael addition-initiated organocatalytic enantioselective multicomponent reactions with 1,3-dicarbonyls : Réactions multicomposants organocatalysées enantiosélectives initiées par l'addition de Michael de dérivés 1,3 dicarbonyles. [Internet] [Doctoral dissertation]. Ecole centrale de Marseille; 2014. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2014ECDM0002.

Council of Science Editors:

Du H. Michael addition-initiated organocatalytic enantioselective multicomponent reactions with 1,3-dicarbonyls : Réactions multicomposants organocatalysées enantiosélectives initiées par l'addition de Michael de dérivés 1,3 dicarbonyles. [Doctoral Dissertation]. Ecole centrale de Marseille; 2014. Available from: http://www.theses.fr/2014ECDM0002

16. Santos, Willian Henrique dos [UNESP]. Estudos sobre a síntese e caracterização de derivados cumarínicos e xantênicos promovida pelo pentacloretro de nióbio.

Degree: 2017, Universidade Estadual Paulista

A demanda por fontes de energias renováveis já é uma necessidade mundial, pois, o crescimento populacional e industrial trouxe concomitantemente um aumento no consumo de… (more)

Subjects/Keywords: Pentacloreto de Nióbio; Reações multicomponentes; Cumarinas; Xantenos; Célula Solar; Niobium Pentachloride; Multicomponent Reactions; Coumarins; Xanthenes; Solar Cell

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APA (6th Edition):

Santos, W. H. d. [. (2017). Estudos sobre a síntese e caracterização de derivados cumarínicos e xantênicos promovida pelo pentacloretro de nióbio. (Thesis). Universidade Estadual Paulista. Retrieved from http://hdl.handle.net/11449/148920

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):

Santos, Willian Henrique dos [UNESP]. “Estudos sobre a síntese e caracterização de derivados cumarínicos e xantênicos promovida pelo pentacloretro de nióbio.” 2017. Thesis, Universidade Estadual Paulista. Accessed October 23, 2019. http://hdl.handle.net/11449/148920.

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

MLA Handbook (7th Edition):

Santos, Willian Henrique dos [UNESP]. “Estudos sobre a síntese e caracterização de derivados cumarínicos e xantênicos promovida pelo pentacloretro de nióbio.” 2017. Web. 23 Oct 2019.

Vancouver:

Santos WHd[. Estudos sobre a síntese e caracterização de derivados cumarínicos e xantênicos promovida pelo pentacloretro de nióbio. [Internet] [Thesis]. Universidade Estadual Paulista; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/11449/148920.

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

Council of Science Editors:

Santos WHd[. Estudos sobre a síntese e caracterização de derivados cumarínicos e xantênicos promovida pelo pentacloretro de nióbio. [Thesis]. Universidade Estadual Paulista; 2017. Available from: http://hdl.handle.net/11449/148920

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

17. Paul, Jérôme. Synthèse de composés β2,3-hydroxy- et aminocarboxylés par réactions domino et multicomposants métallo-catalysées : Synthesis of β2,3-hydroxy- and aminocarboxylated by metallo-catalyzed domino and multicomponents reactions.

Degree: Docteur es, Chimie, 2017, Université Paris-Est

La mise au point de réactions multicomposants métallo-catalysées permet de contribuer au développement d’une chimie plus verte. En effet, l’association des réactions multicomposants avec la… (more)

Subjects/Keywords: Catalyse organométallique; Cobalt; Réactions multicomposants; Β2.3-Hydroxycarboxylé; Β2.3-Aminocarboxylé; Multicomponent reactions; Post-Condensations; Molecular templates; Β2.3-Hydroxycarboxylated; Β2.3-Aminocarboxylated

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

APA (6th Edition):

Paul, J. (2017). Synthèse de composés β2,3-hydroxy- et aminocarboxylés par réactions domino et multicomposants métallo-catalysées : Synthesis of β2,3-hydroxy- and aminocarboxylated by metallo-catalyzed domino and multicomponents reactions. (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2017PESC1167

Chicago Manual of Style (16th Edition):

Paul, Jérôme. “Synthèse de composés β2,3-hydroxy- et aminocarboxylés par réactions domino et multicomposants métallo-catalysées : Synthesis of β2,3-hydroxy- and aminocarboxylated by metallo-catalyzed domino and multicomponents reactions.” 2017. Doctoral Dissertation, Université Paris-Est. Accessed October 23, 2019. http://www.theses.fr/2017PESC1167.

MLA Handbook (7th Edition):

Paul, Jérôme. “Synthèse de composés β2,3-hydroxy- et aminocarboxylés par réactions domino et multicomposants métallo-catalysées : Synthesis of β2,3-hydroxy- and aminocarboxylated by metallo-catalyzed domino and multicomponents reactions.” 2017. Web. 23 Oct 2019.

Vancouver:

Paul J. Synthèse de composés β2,3-hydroxy- et aminocarboxylés par réactions domino et multicomposants métallo-catalysées : Synthesis of β2,3-hydroxy- and aminocarboxylated by metallo-catalyzed domino and multicomponents reactions. [Internet] [Doctoral dissertation]. Université Paris-Est; 2017. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2017PESC1167.

Council of Science Editors:

Paul J. Synthèse de composés β2,3-hydroxy- et aminocarboxylés par réactions domino et multicomposants métallo-catalysées : Synthesis of β2,3-hydroxy- and aminocarboxylated by metallo-catalyzed domino and multicomponents reactions. [Doctoral Dissertation]. Université Paris-Est; 2017. Available from: http://www.theses.fr/2017PESC1167

18. Saxer, Samantha. Synthèse de structures macromoléculaires aromatiques et hétérocycliques originales par voies non conventionnelles : Synthesis of original aromatic and heterocyclic macromolecular structures by unconventional pathways.

Degree: Docteur es, Matériaux, 2018, Lyon

Le travail réalisé dans cette thèse concerne la synthèse de nouvelles structures macromoléculaires aromatiques et hétérocycliques. La synthèse de ces polymères a été envisagée par… (more)

Subjects/Keywords: Matériaux; Polymères aromatiques sulfonés; Polymères hétérocycliques; RMC - Réaction multi-Composants; Materials; Aromatic polymers; Heterocyclic polymers; MCR - Multicomponent reactions; 620.192 072

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APA (6th Edition):

Saxer, S. (2018). Synthèse de structures macromoléculaires aromatiques et hétérocycliques originales par voies non conventionnelles : Synthesis of original aromatic and heterocyclic macromolecular structures by unconventional pathways. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2018LYSEI038

Chicago Manual of Style (16th Edition):

Saxer, Samantha. “Synthèse de structures macromoléculaires aromatiques et hétérocycliques originales par voies non conventionnelles : Synthesis of original aromatic and heterocyclic macromolecular structures by unconventional pathways.” 2018. Doctoral Dissertation, Lyon. Accessed October 23, 2019. http://www.theses.fr/2018LYSEI038.

MLA Handbook (7th Edition):

Saxer, Samantha. “Synthèse de structures macromoléculaires aromatiques et hétérocycliques originales par voies non conventionnelles : Synthesis of original aromatic and heterocyclic macromolecular structures by unconventional pathways.” 2018. Web. 23 Oct 2019.

Vancouver:

Saxer S. Synthèse de structures macromoléculaires aromatiques et hétérocycliques originales par voies non conventionnelles : Synthesis of original aromatic and heterocyclic macromolecular structures by unconventional pathways. [Internet] [Doctoral dissertation]. Lyon; 2018. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2018LYSEI038.

Council of Science Editors:

Saxer S. Synthèse de structures macromoléculaires aromatiques et hétérocycliques originales par voies non conventionnelles : Synthesis of original aromatic and heterocyclic macromolecular structures by unconventional pathways. [Doctoral Dissertation]. Lyon; 2018. Available from: http://www.theses.fr/2018LYSEI038

19. Dudognon, Yohan. Synthèse et utilisation de composés 1,3 - dicarbonylés en organocatalyse énantiosélective : Synthesis and use of compounds 1,3 - diacarbonyl in enantioselective organocatalysis.

Degree: Docteur es, Chimie. Chimie organique, 2016, Aix Marseille Université

Ce mémoire de thèse se concentre sur la mise au point de nouvelles réactions mettant en jeu des composés 1,3-cétoamides en organocatalyse énantiosélective, enfin d’accéder… (more)

Subjects/Keywords: Organocatalyse; 1,3-Cétoamides; Enantiosélectivité; Réaction multi-Composés; Micro-Ondes; Alpha-Fonctionnalisation; Organocatalysis; 1,3-Ketoamides; Enantioselectivity; Multicomponent Reactions; Microwave; Alpha-Functionalization

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

APA (6th Edition):

Dudognon, Y. (2016). Synthèse et utilisation de composés 1,3 - dicarbonylés en organocatalyse énantiosélective : Synthesis and use of compounds 1,3 - diacarbonyl in enantioselective organocatalysis. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM4357

Chicago Manual of Style (16th Edition):

Dudognon, Yohan. “Synthèse et utilisation de composés 1,3 - dicarbonylés en organocatalyse énantiosélective : Synthesis and use of compounds 1,3 - diacarbonyl in enantioselective organocatalysis.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed October 23, 2019. http://www.theses.fr/2016AIXM4357.

MLA Handbook (7th Edition):

Dudognon, Yohan. “Synthèse et utilisation de composés 1,3 - dicarbonylés en organocatalyse énantiosélective : Synthesis and use of compounds 1,3 - diacarbonyl in enantioselective organocatalysis.” 2016. Web. 23 Oct 2019.

Vancouver:

Dudognon Y. Synthèse et utilisation de composés 1,3 - dicarbonylés en organocatalyse énantiosélective : Synthesis and use of compounds 1,3 - diacarbonyl in enantioselective organocatalysis. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2016AIXM4357.

Council of Science Editors:

Dudognon Y. Synthèse et utilisation de composés 1,3 - dicarbonylés en organocatalyse énantiosélective : Synthesis and use of compounds 1,3 - diacarbonyl in enantioselective organocatalysis. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM4357


Vrije Universiteit Amsterdam

20. Scheffelaar, R. Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential .

Degree: 2010, Vrije Universiteit Amsterdam

Subjects/Keywords: Multicomponent Reactions • Diversity-Oriented Synthesis • Complexity • Synthesis • Scaffold Diversity

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APA (6th Edition):

Scheffelaar, R. (2010). Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/16149

Chicago Manual of Style (16th Edition):

Scheffelaar, R. “Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential .” 2010. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 23, 2019. http://hdl.handle.net/1871/16149.

MLA Handbook (7th Edition):

Scheffelaar, R. “Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential .” 2010. Web. 23 Oct 2019.

Vancouver:

Scheffelaar R. Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2010. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1871/16149.

Council of Science Editors:

Scheffelaar R. Isonitrile-Functionalized 3,4-Dihydropyridin-2-ones: Multicomponent Synthesis and Synthetic Potential . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2010. Available from: http://hdl.handle.net/1871/16149

21. Heijden, G. van der. MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals .

Degree: 2018, Vrije Universiteit Amsterdam

Subjects/Keywords: Multicomponent Reactions; Convertible isocyanide; pharmaceuticals; Organic Synthesis

Page 1

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APA (6th Edition):

Heijden, G. v. d. (2018). MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/55516

Chicago Manual of Style (16th Edition):

Heijden, G van der. “MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals .” 2018. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 23, 2019. http://hdl.handle.net/1871/55516.

MLA Handbook (7th Edition):

Heijden, G van der. “MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals .” 2018. Web. 23 Oct 2019.

Vancouver:

Heijden Gvd. MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2018. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1871/55516.

Council of Science Editors:

Heijden Gvd. MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2018. Available from: http://hdl.handle.net/1871/55516

22. Kerim, Mansour Dolé. Des réactions multicomposants aux réactions de Tsuji-Trost des dérivés nitrés et phosphorylés : Multicomponent reactions to Tsuji-Trost reactions of nitro and phosphorylated derivatives.

Degree: Docteur es, Chimie, 2018, Paris Saclay

Les travaux de cette thèse ont porté sur le développement de nouvelles méthodes de synthèse autour de la chimie des réactions multicomposants et des réactions… (more)

Subjects/Keywords: Réactions multicompsants; Tsuji-Trost; Dérivés nitrés; Dérivés phosphorylés; Multicomponent reactions; Tsuji-Trost; Nitro derivatives; Phosphorylated derivatives

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

APA (6th Edition):

Kerim, M. D. (2018). Des réactions multicomposants aux réactions de Tsuji-Trost des dérivés nitrés et phosphorylés : Multicomponent reactions to Tsuji-Trost reactions of nitro and phosphorylated derivatives. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLX115

Chicago Manual of Style (16th Edition):

Kerim, Mansour Dolé. “Des réactions multicomposants aux réactions de Tsuji-Trost des dérivés nitrés et phosphorylés : Multicomponent reactions to Tsuji-Trost reactions of nitro and phosphorylated derivatives.” 2018. Doctoral Dissertation, Paris Saclay. Accessed October 23, 2019. http://www.theses.fr/2018SACLX115.

MLA Handbook (7th Edition):

Kerim, Mansour Dolé. “Des réactions multicomposants aux réactions de Tsuji-Trost des dérivés nitrés et phosphorylés : Multicomponent reactions to Tsuji-Trost reactions of nitro and phosphorylated derivatives.” 2018. Web. 23 Oct 2019.

Vancouver:

Kerim MD. Des réactions multicomposants aux réactions de Tsuji-Trost des dérivés nitrés et phosphorylés : Multicomponent reactions to Tsuji-Trost reactions of nitro and phosphorylated derivatives. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2018SACLX115.

Council of Science Editors:

Kerim MD. Des réactions multicomposants aux réactions de Tsuji-Trost des dérivés nitrés et phosphorylés : Multicomponent reactions to Tsuji-Trost reactions of nitro and phosphorylated derivatives. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLX115

23. Nyadanu, Aude. Nouvelles réactions multicomposants et ouverture de cycles contraints pour la synthèse d’hétérocycles : New multicomponent reactions and constrained rings opening towards heterocycles synthesis.

Degree: Docteur es, Chimie, 2018, Paris Saclay

Les réactions multicomposants (MCR) constituent une réponse à deux grands défis rencontrés par la chimie pharmaceutique : la découverte de nouvelles molécules bioactives ainsi que… (more)

Subjects/Keywords: Chimie organique; Réactions multicomposants; Catalyse au palladium; Cyclopropanes; Soufre; Hétérocycles; Organic chemistry; Multicomponent reactions; Palladium catalysis; Cyclopropane; Sulfur; Heterocyles; 547

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APA (6th Edition):

Nyadanu, A. (2018). Nouvelles réactions multicomposants et ouverture de cycles contraints pour la synthèse d’hétérocycles : New multicomponent reactions and constrained rings opening towards heterocycles synthesis. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLX065

Chicago Manual of Style (16th Edition):

Nyadanu, Aude. “Nouvelles réactions multicomposants et ouverture de cycles contraints pour la synthèse d’hétérocycles : New multicomponent reactions and constrained rings opening towards heterocycles synthesis.” 2018. Doctoral Dissertation, Paris Saclay. Accessed October 23, 2019. http://www.theses.fr/2018SACLX065.

MLA Handbook (7th Edition):

Nyadanu, Aude. “Nouvelles réactions multicomposants et ouverture de cycles contraints pour la synthèse d’hétérocycles : New multicomponent reactions and constrained rings opening towards heterocycles synthesis.” 2018. Web. 23 Oct 2019.

Vancouver:

Nyadanu A. Nouvelles réactions multicomposants et ouverture de cycles contraints pour la synthèse d’hétérocycles : New multicomponent reactions and constrained rings opening towards heterocycles synthesis. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2018SACLX065.

Council of Science Editors:

Nyadanu A. Nouvelles réactions multicomposants et ouverture de cycles contraints pour la synthèse d’hétérocycles : New multicomponent reactions and constrained rings opening towards heterocycles synthesis. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLX065


Wayne State University

24. Santra, Soumava. I. Microwave-Influenced Diversity-Oriented Synthesis Of Biologically Relevant Small & Natural-Product-Like Molecules Via Multicomponent Coupling Reactions Ii. Synthetic Studies Toward The Total Synthesis Of The Repeating Tetrasaccharide Unit Of Zwitterionic Polysaccharide Ps A1.

Degree: PhD, Chemistry, 2010, Wayne State University

  Microwave-influenced diversity-oriented synthesis of biologically relevant small and natural-product-like molecules via multicomponent coupling reactions (MCCRs) have been investigated. Cheap, readily available starting materials in… (more)

Subjects/Keywords: Microwave irradiation; Multicomponent coupling reactions; Neutral glycosylation; PDMAB alcohol; small and natural-product-like molecules; zwitterionic polysaccharide PS A1; Organic Chemistry

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APA (6th Edition):

Santra, S. (2010). I. Microwave-Influenced Diversity-Oriented Synthesis Of Biologically Relevant Small & Natural-Product-Like Molecules Via Multicomponent Coupling Reactions Ii. Synthetic Studies Toward The Total Synthesis Of The Repeating Tetrasaccharide Unit Of Zwitterionic Polysaccharide Ps A1. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/69

Chicago Manual of Style (16th Edition):

Santra, Soumava. “I. Microwave-Influenced Diversity-Oriented Synthesis Of Biologically Relevant Small & Natural-Product-Like Molecules Via Multicomponent Coupling Reactions Ii. Synthetic Studies Toward The Total Synthesis Of The Repeating Tetrasaccharide Unit Of Zwitterionic Polysaccharide Ps A1.” 2010. Doctoral Dissertation, Wayne State University. Accessed October 23, 2019. https://digitalcommons.wayne.edu/oa_dissertations/69.

MLA Handbook (7th Edition):

Santra, Soumava. “I. Microwave-Influenced Diversity-Oriented Synthesis Of Biologically Relevant Small & Natural-Product-Like Molecules Via Multicomponent Coupling Reactions Ii. Synthetic Studies Toward The Total Synthesis Of The Repeating Tetrasaccharide Unit Of Zwitterionic Polysaccharide Ps A1.” 2010. Web. 23 Oct 2019.

Vancouver:

Santra S. I. Microwave-Influenced Diversity-Oriented Synthesis Of Biologically Relevant Small & Natural-Product-Like Molecules Via Multicomponent Coupling Reactions Ii. Synthetic Studies Toward The Total Synthesis Of The Repeating Tetrasaccharide Unit Of Zwitterionic Polysaccharide Ps A1. [Internet] [Doctoral dissertation]. Wayne State University; 2010. [cited 2019 Oct 23]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/69.

Council of Science Editors:

Santra S. I. Microwave-Influenced Diversity-Oriented Synthesis Of Biologically Relevant Small & Natural-Product-Like Molecules Via Multicomponent Coupling Reactions Ii. Synthetic Studies Toward The Total Synthesis Of The Repeating Tetrasaccharide Unit Of Zwitterionic Polysaccharide Ps A1. [Doctoral Dissertation]. Wayne State University; 2010. Available from: https://digitalcommons.wayne.edu/oa_dissertations/69

25. van der Heijden, G. MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals.

Degree: 2018, NARCIS

Subjects/Keywords: Multicomponent Reactions; Convertible isocyanide; pharmaceuticals; Organic Synthesis

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APA (6th Edition):

van der Heijden, G. (2018). MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals. (Doctoral Dissertation). NARCIS. Retrieved from https://research.vu.nl/en/publications/9b95c683-48f7-45a9-8d51-55e5f56e0c7b ; urn:nbn:nl:ui:31-1871/55516 ; 9b95c683-48f7-45a9-8d51-55e5f56e0c7b ; 1871/55516 ; urn:nbn:nl:ui:31-1871/55516 ; https://research.vu.nl/en/publications/9b95c683-48f7-45a9-8d51-55e5f56e0c7b

Chicago Manual of Style (16th Edition):

van der Heijden, G. “MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals.” 2018. Doctoral Dissertation, NARCIS. Accessed October 23, 2019. https://research.vu.nl/en/publications/9b95c683-48f7-45a9-8d51-55e5f56e0c7b ; urn:nbn:nl:ui:31-1871/55516 ; 9b95c683-48f7-45a9-8d51-55e5f56e0c7b ; 1871/55516 ; urn:nbn:nl:ui:31-1871/55516 ; https://research.vu.nl/en/publications/9b95c683-48f7-45a9-8d51-55e5f56e0c7b.

MLA Handbook (7th Edition):

van der Heijden, G. “MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals.” 2018. Web. 23 Oct 2019.

Vancouver:

van der Heijden G. MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals. [Internet] [Doctoral dissertation]. NARCIS; 2018. [cited 2019 Oct 23]. Available from: https://research.vu.nl/en/publications/9b95c683-48f7-45a9-8d51-55e5f56e0c7b ; urn:nbn:nl:ui:31-1871/55516 ; 9b95c683-48f7-45a9-8d51-55e5f56e0c7b ; 1871/55516 ; urn:nbn:nl:ui:31-1871/55516 ; https://research.vu.nl/en/publications/9b95c683-48f7-45a9-8d51-55e5f56e0c7b.

Council of Science Editors:

van der Heijden G. MCRs to APIs: Tailoring Multicomponent Reactions for the Production of Pharmaceuticals. [Doctoral Dissertation]. NARCIS; 2018. Available from: https://research.vu.nl/en/publications/9b95c683-48f7-45a9-8d51-55e5f56e0c7b ; urn:nbn:nl:ui:31-1871/55516 ; 9b95c683-48f7-45a9-8d51-55e5f56e0c7b ; 1871/55516 ; urn:nbn:nl:ui:31-1871/55516 ; https://research.vu.nl/en/publications/9b95c683-48f7-45a9-8d51-55e5f56e0c7b

26. Sanchez Duque, Maria del Mar. Nouvelles applications de l'addition de Michael organo catalysée dans des réactions domino multicomposés énantiosélectives : Imprints of environmental changes on the phylogeography of the genus Myrtus in the Mediterranean and the Sahara.

Degree: Docteur es, Chimie organique, 2011, Aix-Marseille 3

Au cours de ce travail, nous nous sommes intéressés à explorer le potentiel d’une réaction multicomposés initiée par une addition de Michael conduisant à des… (more)

Subjects/Keywords: Organocatalyse; Réactions multicomposés; Réactions domino; Addition de Michael; Énantiosélectivité; Spiro hétérocycles; Béta-cétoamides; Organocatalysis; Multicomponent reactions; Domino reactions; Michael addition; Enantioselectivity; Spiro heterocycles; Beta-ketoamides

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

APA (6th Edition):

Sanchez Duque, M. d. M. (2011). Nouvelles applications de l'addition de Michael organo catalysée dans des réactions domino multicomposés énantiosélectives : Imprints of environmental changes on the phylogeography of the genus Myrtus in the Mediterranean and the Sahara. (Doctoral Dissertation). Aix-Marseille 3. Retrieved from http://www.theses.fr/2011AIX30047

Chicago Manual of Style (16th Edition):

Sanchez Duque, Maria del Mar. “Nouvelles applications de l'addition de Michael organo catalysée dans des réactions domino multicomposés énantiosélectives : Imprints of environmental changes on the phylogeography of the genus Myrtus in the Mediterranean and the Sahara.” 2011. Doctoral Dissertation, Aix-Marseille 3. Accessed October 23, 2019. http://www.theses.fr/2011AIX30047.

MLA Handbook (7th Edition):

Sanchez Duque, Maria del Mar. “Nouvelles applications de l'addition de Michael organo catalysée dans des réactions domino multicomposés énantiosélectives : Imprints of environmental changes on the phylogeography of the genus Myrtus in the Mediterranean and the Sahara.” 2011. Web. 23 Oct 2019.

Vancouver:

Sanchez Duque MdM. Nouvelles applications de l'addition de Michael organo catalysée dans des réactions domino multicomposés énantiosélectives : Imprints of environmental changes on the phylogeography of the genus Myrtus in the Mediterranean and the Sahara. [Internet] [Doctoral dissertation]. Aix-Marseille 3; 2011. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2011AIX30047.

Council of Science Editors:

Sanchez Duque MdM. Nouvelles applications de l'addition de Michael organo catalysée dans des réactions domino multicomposés énantiosélectives : Imprints of environmental changes on the phylogeography of the genus Myrtus in the Mediterranean and the Sahara. [Doctoral Dissertation]. Aix-Marseille 3; 2011. Available from: http://www.theses.fr/2011AIX30047


Vrije Universiteit Amsterdam

27. Bon, R.S. Development and application of novel multicomponent reactions using (a)alfa-acidic isocyanides .

Degree: 2007, Vrije Universiteit Amsterdam

 The research described in this thesis deals with: i) the exploitation of the a-acidity of isocyanides in the development of new multicomponent reactions; ii) the… (more)

Subjects/Keywords: Catalytic asymmetric Ugi-reactions; multicomponent reactions; isocyanides; N-heterocyclic carbenes; imidazolines; dihydropyridones; Nutlins

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APA (6th Edition):

Bon, R. S. (2007). Development and application of novel multicomponent reactions using (a)alfa-acidic isocyanides . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/10882

Chicago Manual of Style (16th Edition):

Bon, R S. “Development and application of novel multicomponent reactions using (a)alfa-acidic isocyanides .” 2007. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 23, 2019. http://hdl.handle.net/1871/10882.

MLA Handbook (7th Edition):

Bon, R S. “Development and application of novel multicomponent reactions using (a)alfa-acidic isocyanides .” 2007. Web. 23 Oct 2019.

Vancouver:

Bon RS. Development and application of novel multicomponent reactions using (a)alfa-acidic isocyanides . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2007. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1871/10882.

Council of Science Editors:

Bon RS. Development and application of novel multicomponent reactions using (a)alfa-acidic isocyanides . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2007. Available from: http://hdl.handle.net/1871/10882

28. Bindu,S. Novel Hetrocyclic Constructions Mediated by Nucleophilic Carbenes and Related Chemistry.

Degree: 2003, Cochin University of Science and Technology

 The thesis entitled novel heterocyclic constructions mediated by nucleophilic carbenes and related chemistry, embodies the results of the investigations carried out to explore the reactivity… (more)

Subjects/Keywords: Heterocyclic compounds; Nucleophilic carbenes; DiMethyl AcetyleneDicarboxylate(DMAD); Multicomponent reactions(MCRs)

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APA (6th Edition):

Bindu,S. (2003). Novel Hetrocyclic Constructions Mediated by Nucleophilic Carbenes and Related Chemistry. (Thesis). Cochin University of Science and Technology. Retrieved from http://dyuthi.cusat.ac.in/purl/23

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

Chicago Manual of Style (16th Edition):

Bindu,S. “Novel Hetrocyclic Constructions Mediated by Nucleophilic Carbenes and Related Chemistry.” 2003. Thesis, Cochin University of Science and Technology. Accessed October 23, 2019. http://dyuthi.cusat.ac.in/purl/23.

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

MLA Handbook (7th Edition):

Bindu,S. “Novel Hetrocyclic Constructions Mediated by Nucleophilic Carbenes and Related Chemistry.” 2003. Web. 23 Oct 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Bindu,S. Novel Hetrocyclic Constructions Mediated by Nucleophilic Carbenes and Related Chemistry. [Internet] [Thesis]. Cochin University of Science and Technology; 2003. [cited 2019 Oct 23]. Available from: http://dyuthi.cusat.ac.in/purl/23.

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

Council of Science Editors:

Bindu,S. Novel Hetrocyclic Constructions Mediated by Nucleophilic Carbenes and Related Chemistry. [Thesis]. Cochin University of Science and Technology; 2003. Available from: http://dyuthi.cusat.ac.in/purl/23

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


EPFL

29. Christinat, Nicolas. Self-assembly of boron-based supramolecular structures.

Degree: 2008, EPFL

 This work describes the synthesis and characterization of boronic acid-based supramolecular structures. Macrocycles, dendritic structures, polymers, rotaxanes, and cages were assembled using four types of… (more)

Subjects/Keywords: Boronic acids; Self-assembly; Macrocycles; Imine; Multicomponent reactions; Polymers; Rotaxanes; Cages; Acides boroniques; Auto-assemblage; Macrocycles; Imines; Réactions à composants multiples; Polymères; Rotaxanes; Cages

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APA (6th Edition):

Christinat, N. (2008). Self-assembly of boron-based supramolecular structures. (Thesis). EPFL. Retrieved from http://infoscience.epfl.ch/record/125888

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):

Christinat, Nicolas. “Self-assembly of boron-based supramolecular structures.” 2008. Thesis, EPFL. Accessed October 23, 2019. http://infoscience.epfl.ch/record/125888.

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

MLA Handbook (7th Edition):

Christinat, Nicolas. “Self-assembly of boron-based supramolecular structures.” 2008. Web. 23 Oct 2019.

Vancouver:

Christinat N. Self-assembly of boron-based supramolecular structures. [Internet] [Thesis]. EPFL; 2008. [cited 2019 Oct 23]. Available from: http://infoscience.epfl.ch/record/125888.

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

Council of Science Editors:

Christinat N. Self-assembly of boron-based supramolecular structures. [Thesis]. EPFL; 2008. Available from: http://infoscience.epfl.ch/record/125888

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

30. Benchekroun, Mohamed. Synthèse multicomposants et évaluation pharmacologique de nouveaux adduits de Ugi et de Passerini pour le traitement de la maladie d'Alzheimer : Multicomponent synthesis and pharmacological assessment of new Ugi and Passerini adducts for the treatment of Alzheimer’s disease.

Degree: Docteur es, Sciences de la vie et de la santé, 2014, Besançon

La maladie d'Alzheimer est la pathologie neurodégénérative la plus courante affectant les personnes âgées. Cette neuropathologie se caractérise par une étiologie complexe dont le déficit… (more)

Subjects/Keywords: Maladie d'Alzheimer; Réactions multicomposants; Inhibiteurs des cholinestérases; Antioxydants; Hépatotoxicité; Neuroprotection; Alzheimer's disease; Multicomponent reactions; Cholinesterase inhibitors; Antioxidants; Hepatotoxicity; Neuroprotection; 610; WT 155

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APA (6th Edition):

Benchekroun, M. (2014). Synthèse multicomposants et évaluation pharmacologique de nouveaux adduits de Ugi et de Passerini pour le traitement de la maladie d'Alzheimer : Multicomponent synthesis and pharmacological assessment of new Ugi and Passerini adducts for the treatment of Alzheimer’s disease. (Doctoral Dissertation). Besançon. Retrieved from http://www.theses.fr/2014BESA3007

Chicago Manual of Style (16th Edition):

Benchekroun, Mohamed. “Synthèse multicomposants et évaluation pharmacologique de nouveaux adduits de Ugi et de Passerini pour le traitement de la maladie d'Alzheimer : Multicomponent synthesis and pharmacological assessment of new Ugi and Passerini adducts for the treatment of Alzheimer’s disease.” 2014. Doctoral Dissertation, Besançon. Accessed October 23, 2019. http://www.theses.fr/2014BESA3007.

MLA Handbook (7th Edition):

Benchekroun, Mohamed. “Synthèse multicomposants et évaluation pharmacologique de nouveaux adduits de Ugi et de Passerini pour le traitement de la maladie d'Alzheimer : Multicomponent synthesis and pharmacological assessment of new Ugi and Passerini adducts for the treatment of Alzheimer’s disease.” 2014. Web. 23 Oct 2019.

Vancouver:

Benchekroun M. Synthèse multicomposants et évaluation pharmacologique de nouveaux adduits de Ugi et de Passerini pour le traitement de la maladie d'Alzheimer : Multicomponent synthesis and pharmacological assessment of new Ugi and Passerini adducts for the treatment of Alzheimer’s disease. [Internet] [Doctoral dissertation]. Besançon; 2014. [cited 2019 Oct 23]. Available from: http://www.theses.fr/2014BESA3007.

Council of Science Editors:

Benchekroun M. Synthèse multicomposants et évaluation pharmacologique de nouveaux adduits de Ugi et de Passerini pour le traitement de la maladie d'Alzheimer : Multicomponent synthesis and pharmacological assessment of new Ugi and Passerini adducts for the treatment of Alzheimer’s disease. [Doctoral Dissertation]. Besançon; 2014. Available from: http://www.theses.fr/2014BESA3007

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