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You searched for subject:(Ring contraction). Showing records 1 – 18 of 18 total matches.

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Université Montpellier II

1. Chaubet, Guilhem. Nouvelles réactions de contraction de cycle : outils pour la construction d'édifices organisés : New ring contraction reactions : tools for the construction of organised edifices.

Degree: Docteur es, Ingénierie moléculaire, 2013, Université Montpellier II

Ces travaux de thèse s'inscrivent dans un projet à long terme concernant le développement de nouvelles réactions de contraction de cycle originales afin d'accéder à… (more)

Subjects/Keywords: Réactions de contraction de cycle; Synthèse stéréosélective; Spirolactames; Hélice de polyproline II; Ring contraction reactions; Stereoselective synthesis; Spirolactams; Polyproline II helix

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APA (6th Edition):

Chaubet, G. (2013). Nouvelles réactions de contraction de cycle : outils pour la construction d'édifices organisés : New ring contraction reactions : tools for the construction of organised edifices. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2013MON20119

Chicago Manual of Style (16th Edition):

Chaubet, Guilhem. “Nouvelles réactions de contraction de cycle : outils pour la construction d'édifices organisés : New ring contraction reactions : tools for the construction of organised edifices.” 2013. Doctoral Dissertation, Université Montpellier II. Accessed July 15, 2020. http://www.theses.fr/2013MON20119.

MLA Handbook (7th Edition):

Chaubet, Guilhem. “Nouvelles réactions de contraction de cycle : outils pour la construction d'édifices organisés : New ring contraction reactions : tools for the construction of organised edifices.” 2013. Web. 15 Jul 2020.

Vancouver:

Chaubet G. Nouvelles réactions de contraction de cycle : outils pour la construction d'édifices organisés : New ring contraction reactions : tools for the construction of organised edifices. [Internet] [Doctoral dissertation]. Université Montpellier II; 2013. [cited 2020 Jul 15]. Available from: http://www.theses.fr/2013MON20119.

Council of Science Editors:

Chaubet G. Nouvelles réactions de contraction de cycle : outils pour la construction d'édifices organisés : New ring contraction reactions : tools for the construction of organised edifices. [Doctoral Dissertation]. Université Montpellier II; 2013. Available from: http://www.theses.fr/2013MON20119

2. Feraldi-Xypolia, Alexandra. Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés.

Degree: Docteur es, Chimie Organique, 2017, Université Pierre et Marie Curie – Paris VI

L’introduction d’un atome de fluor sur un composé organique peut avoir une influence importante sur les propriétés chimiques et physico-chimiques de ce composé, ainsi qu’à… (more)

Subjects/Keywords: Contraction de cycle; Αlpha-(trifluorométhyl)pyrrolidines; Αlapha-(trifluorométhyl)pipéridines; Aziridinium; Cycloaddition; Alpha – (trifluorométhyl)pyridazines; Ring contraction; Cycloaddition; Trifluoromethyl; 547

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APA (6th Edition):

Feraldi-Xypolia, A. (2017). Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066444

Chicago Manual of Style (16th Edition):

Feraldi-Xypolia, Alexandra. “Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed July 15, 2020. http://www.theses.fr/2017PA066444.

MLA Handbook (7th Edition):

Feraldi-Xypolia, Alexandra. “Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés.” 2017. Web. 15 Jul 2020.

Vancouver:

Feraldi-Xypolia A. Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2020 Jul 15]. Available from: http://www.theses.fr/2017PA066444.

Council of Science Editors:

Feraldi-Xypolia A. Synthesis of trifluoromethylated nitrogen-containing heterocycles : Synthèse d'hétérocycles azotés et trifluorométhylés. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066444

3. Fontelle, Nathalie. Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2013, Poitiers

Les iminosucres, analogues de sucres dont l'oxygène intracyclique a été remplacé par un azote, constituent une classe importante de mimes de sucres. Introduire une chaîne… (more)

Subjects/Keywords: Iminosucres C-Glycosides; Iminosucres-Aza-Couronne; N-Acétyl-D-Glucosamine; Contraction de cycle; Glycosidases; Iminosugars C-Glycosides; Iminosugars-Aza-Crown; N-Acetyl-D-Glucosamine; Ring contraction; Glycosidases; 547

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APA (6th Edition):

Fontelle, N. (2013). Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine. (Doctoral Dissertation). Poitiers. Retrieved from http://www.theses.fr/2013POIT2334

Chicago Manual of Style (16th Edition):

Fontelle, Nathalie. “Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine.” 2013. Doctoral Dissertation, Poitiers. Accessed July 15, 2020. http://www.theses.fr/2013POIT2334.

MLA Handbook (7th Edition):

Fontelle, Nathalie. “Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine.” 2013. Web. 15 Jul 2020.

Vancouver:

Fontelle N. Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine. [Internet] [Doctoral dissertation]. Poitiers; 2013. [cited 2020 Jul 15]. Available from: http://www.theses.fr/2013POIT2334.

Council of Science Editors:

Fontelle N. Mise au point d'une nouvelle voie d'accès aux iminosucres C-glycosides à six et sept chaînons dérivés du D-glucopyranose et de la N-acétyl-D-glucosamine : Design of new synthetic route of six and seven membered iminosugar-C-glycosides derived from D-glucopyranose and N-acetyl-D-glucosamine. [Doctoral Dissertation]. Poitiers; 2013. Available from: http://www.theses.fr/2013POIT2334


Bowling Green State University

4. Karpov, Grigori V. Activation of Enediynes by Photochemical Ring Contraction: Design, Synthesis and Reactivity of Cyclic Enediynes Containing Diazodicarbonyl Moiety.

Degree: PhD, Photochemical Sciences, 2006, Bowling Green State University

 Of all recently discovered antibiotics, the natural enediyne antibiotics possibly show the most promise as prospective drugs for the treatment of various forms of cancer.… (more)

Subjects/Keywords: Chemistry, Organic; Photochemistry; Enediynes; Bergman Cyclization; Ring Contraction; Diazodiketones; Wolff Rearrangement

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APA (6th Edition):

Karpov, G. V. (2006). Activation of Enediynes by Photochemical Ring Contraction: Design, Synthesis and Reactivity of Cyclic Enediynes Containing Diazodicarbonyl Moiety. (Doctoral Dissertation). Bowling Green State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1134408707

Chicago Manual of Style (16th Edition):

Karpov, Grigori V. “Activation of Enediynes by Photochemical Ring Contraction: Design, Synthesis and Reactivity of Cyclic Enediynes Containing Diazodicarbonyl Moiety.” 2006. Doctoral Dissertation, Bowling Green State University. Accessed July 15, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1134408707.

MLA Handbook (7th Edition):

Karpov, Grigori V. “Activation of Enediynes by Photochemical Ring Contraction: Design, Synthesis and Reactivity of Cyclic Enediynes Containing Diazodicarbonyl Moiety.” 2006. Web. 15 Jul 2020.

Vancouver:

Karpov GV. Activation of Enediynes by Photochemical Ring Contraction: Design, Synthesis and Reactivity of Cyclic Enediynes Containing Diazodicarbonyl Moiety. [Internet] [Doctoral dissertation]. Bowling Green State University; 2006. [cited 2020 Jul 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1134408707.

Council of Science Editors:

Karpov GV. Activation of Enediynes by Photochemical Ring Contraction: Design, Synthesis and Reactivity of Cyclic Enediynes Containing Diazodicarbonyl Moiety. [Doctoral Dissertation]. Bowling Green State University; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1134408707

5. Carneiro, Vânia Maria Teixeira. Síntese total da (+)-baquenolida A, oxidação de cis-octalinas e de 1,2-di-hidronaftalenos com tálio(III) e síntese de reagentes de Koser.

Degree: PhD, Química Orgânica, 2011, University of São Paulo

A primeira parte deste trabalho teve como objetivo a síntese da (+)-baquenolida A empregando uma reação de contração de anel como etapa chave. A molécula… (more)

Subjects/Keywords: (+)-Bakkenolide A; (+)-Baquenolida A; Contração de anel; Hypervalent iodine; Iodo hipervalente; Organic synthesis; Ring contraction; Síntese orgânica; Síntese total; Tálio(III); Thallium(III); Total synthesis

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APA (6th Edition):

Carneiro, V. M. T. (2011). Síntese total da (+)-baquenolida A, oxidação de cis-octalinas e de 1,2-di-hidronaftalenos com tálio(III) e síntese de reagentes de Koser. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-12042011-134335/ ;

Chicago Manual of Style (16th Edition):

Carneiro, Vânia Maria Teixeira. “Síntese total da (+)-baquenolida A, oxidação de cis-octalinas e de 1,2-di-hidronaftalenos com tálio(III) e síntese de reagentes de Koser.” 2011. Doctoral Dissertation, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-12042011-134335/ ;.

MLA Handbook (7th Edition):

Carneiro, Vânia Maria Teixeira. “Síntese total da (+)-baquenolida A, oxidação de cis-octalinas e de 1,2-di-hidronaftalenos com tálio(III) e síntese de reagentes de Koser.” 2011. Web. 15 Jul 2020.

Vancouver:

Carneiro VMT. Síntese total da (+)-baquenolida A, oxidação de cis-octalinas e de 1,2-di-hidronaftalenos com tálio(III) e síntese de reagentes de Koser. [Internet] [Doctoral dissertation]. University of São Paulo; 2011. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-12042011-134335/ ;.

Council of Science Editors:

Carneiro VMT. Síntese total da (+)-baquenolida A, oxidação de cis-octalinas e de 1,2-di-hidronaftalenos com tálio(III) e síntese de reagentes de Koser. [Doctoral Dissertation]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-12042011-134335/ ;

6. Tébéka, Iris Raquel Maia. Síntese total da (+)-trans-triquentrina A.

Degree: PhD, Química, 2012, University of São Paulo

Apresenta-se, nesta tese, a síntese total do alcaloide marinho (+)-trans-triquentrina A. Três abordagens foram investigadas como estratégias sintéticas: uma adição conjugada assimétrica, um acoplamento arílico… (more)

Subjects/Keywords: (+)-trans-trikentrin A; (+)-trans-triquentrina A; Antiproliferative activity; Atividade antiproliferativa; Contração de anel; Indol; Indole; Kinetic resolution; Organic synthesis; Resolução cinética; Ring contraction; Síntese orgânica

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APA (6th Edition):

Tébéka, I. R. M. (2012). Síntese total da (+)-trans-triquentrina A. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46136/tde-26042013-113225/ ;

Chicago Manual of Style (16th Edition):

Tébéka, Iris Raquel Maia. “Síntese total da (+)-trans-triquentrina A.” 2012. Doctoral Dissertation, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-26042013-113225/ ;.

MLA Handbook (7th Edition):

Tébéka, Iris Raquel Maia. “Síntese total da (+)-trans-triquentrina A.” 2012. Web. 15 Jul 2020.

Vancouver:

Tébéka IRM. Síntese total da (+)-trans-triquentrina A. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-26042013-113225/ ;.

Council of Science Editors:

Tébéka IRM. Síntese total da (+)-trans-triquentrina A. [Doctoral Dissertation]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-26042013-113225/ ;

7. Ahmad, Anees. Exploring the iodine(III)-mediated ring contraction: new substrates, novel conditions and asymmetric reactions.

Degree: PhD, Química, 2015, University of São Paulo

In the first section this thesis includes the reactivity of various oxygen-containing benzofused cyclic alkenes with HTIB (Hydroxy(tosyloxy)iodobenzene). Instead of getting ring contraction products, 2H-chromene… (more)

Subjects/Keywords: Benzofuranos; Benzofurans; Chiral iodine(III); Chromanes; Contração de anel; Cromanos; Hypervalent iodine; Indane; Indano; Iodo hipervalente; Iodo quiral (III); Organic synthesis; Oxidative rearrangement; Rearranjo oxidativo; Ring contraction; Síntese orgânica

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APA (6th Edition):

Ahmad, A. (2015). Exploring the iodine(III)-mediated ring contraction: new substrates, novel conditions and asymmetric reactions. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46136/tde-29092015-145020/ ;

Chicago Manual of Style (16th Edition):

Ahmad, Anees. “Exploring the iodine(III)-mediated ring contraction: new substrates, novel conditions and asymmetric reactions.” 2015. Doctoral Dissertation, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46136/tde-29092015-145020/ ;.

MLA Handbook (7th Edition):

Ahmad, Anees. “Exploring the iodine(III)-mediated ring contraction: new substrates, novel conditions and asymmetric reactions.” 2015. Web. 15 Jul 2020.

Vancouver:

Ahmad A. Exploring the iodine(III)-mediated ring contraction: new substrates, novel conditions and asymmetric reactions. [Internet] [Doctoral dissertation]. University of São Paulo; 2015. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-29092015-145020/ ;.

Council of Science Editors:

Ahmad A. Exploring the iodine(III)-mediated ring contraction: new substrates, novel conditions and asymmetric reactions. [Doctoral Dissertation]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-29092015-145020/ ;

8. Bianco, Graziela Gallego. Síntese assimétrica do (+)- e do (-)-mutisiantol e obtenção de 1-tetralóis opticamente ativos.

Degree: PhD, Química Orgânica, 2008, University of São Paulo

Esta tese descreve a primeira síntese assimétrica do sesquiterpeno fenólico (+)-(1S, 3R)-mutisiantol, assim como de seu enantiômero não-natural. O (+)-mutisiantol foi obtido em 11 etapas… (more)

Subjects/Keywords: (+)-mutisianthol; (+)-mutisiantol; 1-tetralóis; 1-tetralols; Asymmetric hydrogenation; Biotransformation; Botransformações; Contração de anel; Hidrogenação assimétrica; Iodo (Estudo); Organic synthesis; Produtos naturais; Ring contraction; Síntese orgânica; Tálio(III); Thallium(III)

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APA (6th Edition):

Bianco, G. G. (2008). Síntese assimétrica do (+)- e do (-)-mutisiantol e obtenção de 1-tetralóis opticamente ativos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-30092008-092524/ ;

Chicago Manual of Style (16th Edition):

Bianco, Graziela Gallego. “Síntese assimétrica do (+)- e do (-)-mutisiantol e obtenção de 1-tetralóis opticamente ativos.” 2008. Doctoral Dissertation, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-30092008-092524/ ;.

MLA Handbook (7th Edition):

Bianco, Graziela Gallego. “Síntese assimétrica do (+)- e do (-)-mutisiantol e obtenção de 1-tetralóis opticamente ativos.” 2008. Web. 15 Jul 2020.

Vancouver:

Bianco GG. Síntese assimétrica do (+)- e do (-)-mutisiantol e obtenção de 1-tetralóis opticamente ativos. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-30092008-092524/ ;.

Council of Science Editors:

Bianco GG. Síntese assimétrica do (+)- e do (-)-mutisiantol e obtenção de 1-tetralóis opticamente ativos. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-30092008-092524/ ;


University of Illinois – Chicago

9. Volchkov, Ivan. Development and Application of New Spiroketalization and Allylic Transposition.

Degree: 2014, University of Illinois – Chicago

 The direct rhenium-catalyzed [1,3]-transposition of allylic alcohols and their silyl ethers is a powerful synthetic tool for the preparation of less accessible isomer from a… (more)

Subjects/Keywords: Alder-ene reaction; allylic [1,3]-transposition; ring closing metathesis; enyne metathesis; total synthesis; (–)-dactylolide; bis-spiroketal; diynediol; gold catalyst; hydroalkoxylation; hydration; alcoholysis; ring-contractive allylic transposition; ring contraction; eight-membered; cyclic silyl ether; siloxacycle; six-membered; siloxadiene; siloxene; rhenium(VII) oxide; Re2O7; allyl transfer–alcoholysis; (–)-amphidinolide V; base-catalyzed; alkynyl silane alcoholysis; proline-mediated; direct cross-aldol condensation; aldol condensation

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APA (6th Edition):

Volchkov, I. (2014). Development and Application of New Spiroketalization and Allylic Transposition. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/18897

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):

Volchkov, Ivan. “Development and Application of New Spiroketalization and Allylic Transposition.” 2014. Thesis, University of Illinois – Chicago. Accessed July 15, 2020. http://hdl.handle.net/10027/18897.

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

MLA Handbook (7th Edition):

Volchkov, Ivan. “Development and Application of New Spiroketalization and Allylic Transposition.” 2014. Web. 15 Jul 2020.

Vancouver:

Volchkov I. Development and Application of New Spiroketalization and Allylic Transposition. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/10027/18897.

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

Council of Science Editors:

Volchkov I. Development and Application of New Spiroketalization and Allylic Transposition. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/18897

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

10. Pedrozo, Eliane Corrêa. Reações de ésteres ß,Y-insaturados com tálio(III) e de 1,2-di-hidronaftalenos com iodo(III).

Degree: Mestrado, Química Orgânica, 2006, University of São Paulo

Esta dissertação apresenta um estudo sobre a contração de anel de ésteres ß,y-insaturados promovida por trinitrato de tálio (TTN) e de 1,2-di-hidronaftalenos promovida por hidroxi(tosiloxi)iodobenzeno… (more)

Subjects/Keywords: Contração de anel; Di-hidronaftalenos; Dihydronaphthalenes; Ésteres insaturados; Hidroxi(tosiloxi)iodobenzeno; Hydroxy(tosyloxy)iodobenzene; Indanes; Indano; Ring contraction; Unsaturated esters

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APA (6th Edition):

Pedrozo, E. C. (2006). Reações de ésteres ß,Y-insaturados com tálio(III) e de 1,2-di-hidronaftalenos com iodo(III). (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-28112006-144242/ ;

Chicago Manual of Style (16th Edition):

Pedrozo, Eliane Corrêa. “Reações de ésteres ß,Y-insaturados com tálio(III) e de 1,2-di-hidronaftalenos com iodo(III).” 2006. Masters Thesis, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-28112006-144242/ ;.

MLA Handbook (7th Edition):

Pedrozo, Eliane Corrêa. “Reações de ésteres ß,Y-insaturados com tálio(III) e de 1,2-di-hidronaftalenos com iodo(III).” 2006. Web. 15 Jul 2020.

Vancouver:

Pedrozo EC. Reações de ésteres ß,Y-insaturados com tálio(III) e de 1,2-di-hidronaftalenos com iodo(III). [Internet] [Masters thesis]. University of São Paulo; 2006. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-28112006-144242/ ;.

Council of Science Editors:

Pedrozo EC. Reações de ésteres ß,Y-insaturados com tálio(III) e de 1,2-di-hidronaftalenos com iodo(III). [Masters Thesis]. University of São Paulo; 2006. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-28112006-144242/ ;

11. Craveiro, Marcus Vinicius. Síntese total diastereosseletiva da (±)-trans-triquentrina A.

Degree: PhD, Química Orgânica, 2009, University of São Paulo

Esta tese descreve uma nova abordagem para a síntese de ciclopenta[g]indóis baseada na reação de contração de anel mediada por trinitrato de tálio (TTN) de… (more)

Subjects/Keywords: (±)-trans-trikentrin A; (±)-trans-triquentrina A; Ciclopenta[g]indóis; Contração de anel; Cyclopenta[g]indole; Organic reactions; Organic synthesis; Oxidação (Química); Produtos naturais; Reações orgânicas; Ring contraction; Síntese orgânica; Tálio(III); Thallium(III)

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APA (6th Edition):

Craveiro, M. V. (2009). Síntese total diastereosseletiva da (±)-trans-triquentrina A. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-29072009-085508/ ;

Chicago Manual of Style (16th Edition):

Craveiro, Marcus Vinicius. “Síntese total diastereosseletiva da (±)-trans-triquentrina A.” 2009. Doctoral Dissertation, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-29072009-085508/ ;.

MLA Handbook (7th Edition):

Craveiro, Marcus Vinicius. “Síntese total diastereosseletiva da (±)-trans-triquentrina A.” 2009. Web. 15 Jul 2020.

Vancouver:

Craveiro MV. Síntese total diastereosseletiva da (±)-trans-triquentrina A. [Internet] [Doctoral dissertation]. University of São Paulo; 2009. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-29072009-085508/ ;.

Council of Science Editors:

Craveiro MV. Síntese total diastereosseletiva da (±)-trans-triquentrina A. [Doctoral Dissertation]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-29072009-085508/ ;

12. Quintiliano, Samir Augusto Pino. Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina.

Degree: PhD, Química Orgânica, 2010, University of São Paulo

Abordaram-se diversos aspectos da reação de contração de álcoois homoalílicos promovida por trinitrato de tálio (TTN). A configuração relativa do indano obtido como produto foi… (more)

Subjects/Keywords: Carambola (pesquisa); Caramboxin; Caramboxina; Ciclização de Prins; Contração de anel; Hypervalent iodine; Iodine; Iodo; Iodo hipervalente; Organic reactions; Organic synthesis; Prins cyclization; Reações orgânicas; Ring contraction; Síntese orgânica; Thallium trinitrate; Toxinas; Toxins; Trinitrato de tálio

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

APA (6th Edition):

Quintiliano, S. A. P. (2010). Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-27042010-082909/ ;

Chicago Manual of Style (16th Edition):

Quintiliano, Samir Augusto Pino. “Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina.” 2010. Doctoral Dissertation, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-27042010-082909/ ;.

MLA Handbook (7th Edition):

Quintiliano, Samir Augusto Pino. “Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina.” 2010. Web. 15 Jul 2020.

Vancouver:

Quintiliano SAP. Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-27042010-082909/ ;.

Council of Science Editors:

Quintiliano SAP. Reação de álcoois homoalílicos com tálio(III), iodo e iodo hipervalente, dicloração de cetonas e estudos visando à síntese total da caramboxina. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-27042010-082909/ ;

13. Silva Junior, Luiz Fernando da. Reações de contração de anel promovidas por sais de tálio (III).

Degree: PhD, Química Orgânica, 1999, University of São Paulo

Esta tese apresenta um estudo sobre a contração de anel de olefinas e cetonas cíclicas promovida por sais de tálio(III). A reação de uma série… (more)

Subjects/Keywords: Cetonas; Contração de anel; Ketones; Olefinas; Olefins; Oxidative rearrangement; Rearranjo oxidativo; Ring contraction; Tálio(III); Thallium(III)

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

APA (6th Edition):

Silva Junior, L. F. d. (1999). Reações de contração de anel promovidas por sais de tálio (III). (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-25052007-151439/ ;

Chicago Manual of Style (16th Edition):

Silva Junior, Luiz Fernando da. “Reações de contração de anel promovidas por sais de tálio (III).” 1999. Doctoral Dissertation, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-25052007-151439/ ;.

MLA Handbook (7th Edition):

Silva Junior, Luiz Fernando da. “Reações de contração de anel promovidas por sais de tálio (III).” 1999. Web. 15 Jul 2020.

Vancouver:

Silva Junior LFd. Reações de contração de anel promovidas por sais de tálio (III). [Internet] [Doctoral dissertation]. University of São Paulo; 1999. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-25052007-151439/ ;.

Council of Science Editors:

Silva Junior LFd. Reações de contração de anel promovidas por sais de tálio (III). [Doctoral Dissertation]. University of São Paulo; 1999. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-25052007-151439/ ;

14. Siqueira, Fernanda Amaral de. Reação de contração de anel de 1,2-di-hidronaftalenos com iodo(III) e sua aplicação na síntese total da (±)-indatralina.

Degree: PhD, Química Orgânica, 2008, University of São Paulo

Esta tese mostra a síntese total da (±)-indatralina, representando uma aplicação sintética das reações de contração de anel de 1,2-di-hidronaftalenos mediadas por iodo(III). A molécula… (more)

Subjects/Keywords: (±)-indatralina; (±)-indatraline; 1,2-dihydronaphthalenes; Contração de anel; Di-hidronaftalenos; Drogas de abuso (pesquisa); Indanos; indans; iodine(III); Iodo(III); Organic reactions; Organic synthesis; Oxidação; Oxidation; Reações orgânicas; ring contraction; Síntese orgânica

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APA (6th Edition):

Siqueira, F. A. d. (2008). Reação de contração de anel de 1,2-di-hidronaftalenos com iodo(III) e sua aplicação na síntese total da (±)-indatralina. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-30092008-085852/ ;

Chicago Manual of Style (16th Edition):

Siqueira, Fernanda Amaral de. “Reação de contração de anel de 1,2-di-hidronaftalenos com iodo(III) e sua aplicação na síntese total da (±)-indatralina.” 2008. Doctoral Dissertation, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-30092008-085852/ ;.

MLA Handbook (7th Edition):

Siqueira, Fernanda Amaral de. “Reação de contração de anel de 1,2-di-hidronaftalenos com iodo(III) e sua aplicação na síntese total da (±)-indatralina.” 2008. Web. 15 Jul 2020.

Vancouver:

Siqueira FAd. Reação de contração de anel de 1,2-di-hidronaftalenos com iodo(III) e sua aplicação na síntese total da (±)-indatralina. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-30092008-085852/ ;.

Council of Science Editors:

Siqueira FAd. Reação de contração de anel de 1,2-di-hidronaftalenos com iodo(III) e sua aplicação na síntese total da (±)-indatralina. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-30092008-085852/ ;

15. Aguilar, Andréa Maria. Aplicação de trinitrato de tálio na preparação de indanos e na síntese total do mutisiantol.

Degree: PhD, Química Orgânica, 2003, University of São Paulo

Esta tese apresenta a primeira aplicação sintética da metodologia desenvolvida em nosso grupo de pesquisa, que se trata da contração de anel de 1,2-diidronaftalenos promovida… (more)

Subjects/Keywords: Contração de anel; Indane; Indano; Multisianthol; Mutisiantol; Organic synthesis; Ring contraction; Síntese orgânica; Thallium trinitrate; Trinitrato de tálio

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APA (6th Edition):

Aguilar, A. M. (2003). Aplicação de trinitrato de tálio na preparação de indanos e na síntese total do mutisiantol. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46135/tde-09092008-095159/ ;

Chicago Manual of Style (16th Edition):

Aguilar, Andréa Maria. “Aplicação de trinitrato de tálio na preparação de indanos e na síntese total do mutisiantol.” 2003. Doctoral Dissertation, University of São Paulo. Accessed July 15, 2020. http://www.teses.usp.br/teses/disponiveis/46/46135/tde-09092008-095159/ ;.

MLA Handbook (7th Edition):

Aguilar, Andréa Maria. “Aplicação de trinitrato de tálio na preparação de indanos e na síntese total do mutisiantol.” 2003. Web. 15 Jul 2020.

Vancouver:

Aguilar AM. Aplicação de trinitrato de tálio na preparação de indanos e na síntese total do mutisiantol. [Internet] [Doctoral dissertation]. University of São Paulo; 2003. [cited 2020 Jul 15]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-09092008-095159/ ;.

Council of Science Editors:

Aguilar AM. Aplicação de trinitrato de tálio na preparação de indanos e na síntese total do mutisiantol. [Doctoral Dissertation]. University of São Paulo; 2003. Available from: http://www.teses.usp.br/teses/disponiveis/46/46135/tde-09092008-095159/ ;


ETH Zürich

16. Zajac, Marian. Catalytic asymmetric formation of β-sultams.

Degree: 2008, ETH Zürich

Subjects/Keywords: SULTAME (ORGANISCHE CHEMIE); ASYMMETRISCHE KATALYSE (CHEMISCHE REAKTIONEN); CYCLOADDITIONEN + CYCLOREVERSIONEN + CYCLOELIMINIERUNG (CHEMISCHE REAKTIONEN); CYCLISIERUNGSREAKTIONEN (CHEMISCHE REAKTIONEN); RINGÖFFNUNGSREAKTIONEN + RINGKONTRAKTIONSREAKTIONEN (CHEMISCHE REAKTIONEN); SULTAMS (ORGANIC CHEMISTRY); ASYMMETRIC CATALYSIS (CHEMICAL REACTIONS); CYCLOADDITIONS + RETROCYCLOADDITIONS + CYCLOELIMINATION (CHEMICAL REACTIONS); CYCLIZATION (CHEMICAL REACTIONS); RING CLEAVAGE REACTIONS + RING CONTRACTION REACTIONS (CHEMICAL REACTIONS); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Zajac, M. (2008). Catalytic asymmetric formation of β-sultams. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/150743

Chicago Manual of Style (16th Edition):

Zajac, Marian. “Catalytic asymmetric formation of β-sultams.” 2008. Doctoral Dissertation, ETH Zürich. Accessed July 15, 2020. http://hdl.handle.net/20.500.11850/150743.

MLA Handbook (7th Edition):

Zajac, Marian. “Catalytic asymmetric formation of β-sultams.” 2008. Web. 15 Jul 2020.

Vancouver:

Zajac M. Catalytic asymmetric formation of β-sultams. [Internet] [Doctoral dissertation]. ETH Zürich; 2008. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/20.500.11850/150743.

Council of Science Editors:

Zajac M. Catalytic asymmetric formation of β-sultams. [Doctoral Dissertation]. ETH Zürich; 2008. Available from: http://hdl.handle.net/20.500.11850/150743


ETH Zürich

17. Koch, Florian Matthias. Sulfene als Intermediate in der Katalyse: Asymmetrische Synthese und Modifikationen von β-Sultonen.

Degree: 2008, ETH Zürich

Subjects/Keywords: ASYMMETRISCHE KATALYSE (CHEMISCHE REAKTIONEN); SULFENE (ORGANISCHE CHEMIE); ASYMMETRISCHE CHEMISCHE SYNTHESE + ENANTIOSELEKTIVE SYNTHESE (ORGANISCHE SYNTHESE); SULTONE (ALIPHATISCHE GESÄTTIGTE KOHLENWASSERSTOFFE); RINGÖFFNUNGSREAKTIONEN + RINGKONTRAKTIONSREAKTIONEN (CHEMISCHE REAKTIONEN); ASYMMETRIC CATALYSIS (CHEMICAL REACTIONS); SULFENES (ORGANIC CHEMISTRY); ASYMMETRIC CHEMICAL SYNTHESIS + ENANTIOSELECTIVE SYNTHESIS (ORGANIC SYNTHESIS); SULTONES (ALIPHATIC SATURATED HYDROCARBONS); RING CLEAVAGE REACTIONS + RING CONTRACTION REACTIONS (CHEMICAL REACTIONS); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Koch, F. M. (2008). Sulfene als Intermediate in der Katalyse: Asymmetrische Synthese und Modifikationen von β-Sultonen. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/150868

Chicago Manual of Style (16th Edition):

Koch, Florian Matthias. “Sulfene als Intermediate in der Katalyse: Asymmetrische Synthese und Modifikationen von β-Sultonen.” 2008. Doctoral Dissertation, ETH Zürich. Accessed July 15, 2020. http://hdl.handle.net/20.500.11850/150868.

MLA Handbook (7th Edition):

Koch, Florian Matthias. “Sulfene als Intermediate in der Katalyse: Asymmetrische Synthese und Modifikationen von β-Sultonen.” 2008. Web. 15 Jul 2020.

Vancouver:

Koch FM. Sulfene als Intermediate in der Katalyse: Asymmetrische Synthese und Modifikationen von β-Sultonen. [Internet] [Doctoral dissertation]. ETH Zürich; 2008. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/20.500.11850/150868.

Council of Science Editors:

Koch FM. Sulfene als Intermediate in der Katalyse: Asymmetrische Synthese und Modifikationen von β-Sultonen. [Doctoral Dissertation]. ETH Zürich; 2008. Available from: http://hdl.handle.net/20.500.11850/150868


ETH Zürich

18. Ebner, Christian. I: Total Synthesis of Pallambins A and B - II: Ti(III)-Mediated Regioselective Epoxide Opening - III: Synthesis of Raman-Active Epoxyisoprostane Analogs.

Degree: 2016, ETH Zürich

Subjects/Keywords: ORGANISCHE SYNTHESE (CHEMIE); DITERPENE (ORGANISCHE CHEMIE); EPOXIDE + OXIRANE (ORGANISCHE CHEMIE); RINGÖFFNUNGSREAKTIONEN + RINGKONTRAKTIONSREAKTIONEN (CHEMISCHE REAKTIONEN); REGIOSELEKTIVE REAKTIONEN + REGIOSELEKTIVE SYNTHESEN (ORGANISCHE SYNTHESE); ORGANIC SYNTHESIS (CHEMISTRY); DITERPENES (ORGANIC CHEMISTRY); EPOXIDES + OXIRANES (ORGANIC CHEMISTRY); RING CLEAVAGE REACTIONS + RING CONTRACTION REACTIONS (CHEMICAL REACTIONS); REGIOSELECTIVE REACTIONS + REGIOSELECTIVE SYNTHESIS (ORGANIC SYNTHESIS); info:eu-repo/classification/ddc/540; Chemistry

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APA (6th Edition):

Ebner, C. (2016). I: Total Synthesis of Pallambins A and B - II: Ti(III)-Mediated Regioselective Epoxide Opening - III: Synthesis of Raman-Active Epoxyisoprostane Analogs. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/155838

Chicago Manual of Style (16th Edition):

Ebner, Christian. “I: Total Synthesis of Pallambins A and B - II: Ti(III)-Mediated Regioselective Epoxide Opening - III: Synthesis of Raman-Active Epoxyisoprostane Analogs.” 2016. Doctoral Dissertation, ETH Zürich. Accessed July 15, 2020. http://hdl.handle.net/20.500.11850/155838.

MLA Handbook (7th Edition):

Ebner, Christian. “I: Total Synthesis of Pallambins A and B - II: Ti(III)-Mediated Regioselective Epoxide Opening - III: Synthesis of Raman-Active Epoxyisoprostane Analogs.” 2016. Web. 15 Jul 2020.

Vancouver:

Ebner C. I: Total Synthesis of Pallambins A and B - II: Ti(III)-Mediated Regioselective Epoxide Opening - III: Synthesis of Raman-Active Epoxyisoprostane Analogs. [Internet] [Doctoral dissertation]. ETH Zürich; 2016. [cited 2020 Jul 15]. Available from: http://hdl.handle.net/20.500.11850/155838.

Council of Science Editors:

Ebner C. I: Total Synthesis of Pallambins A and B - II: Ti(III)-Mediated Regioselective Epoxide Opening - III: Synthesis of Raman-Active Epoxyisoprostane Analogs. [Doctoral Dissertation]. ETH Zürich; 2016. Available from: http://hdl.handle.net/20.500.11850/155838

.