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Synthesis of enones, pyrazolines and pyrrolines with gem-difluoroalkyl side chains

Starting from easily accessible gem-difluoropropargylic derivatives, a DBU-mediated isomerisation affords enones in fair yields with a gem-difluoroalkyl chain. These derivatives were used to prepare pyrazolines and pyrrolines with the desired gem-difluoroalkyl side chain by cyclocondensations in goo...

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Autores principales: El Dine, Assaad Nasr, Khalaf, Ali, Grée, Danielle, Tasseau, Olivier, Fares, Fares, Jaber, Nada, Lesot, Philippe, Hachem, Ali, Grée, René
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817575/
https://www.ncbi.nlm.nih.gov/pubmed/24204405
http://dx.doi.org/10.3762/bjoc.9.230
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author El Dine, Assaad Nasr
Khalaf, Ali
Grée, Danielle
Tasseau, Olivier
Fares, Fares
Jaber, Nada
Lesot, Philippe
Hachem, Ali
Grée, René
author_facet El Dine, Assaad Nasr
Khalaf, Ali
Grée, Danielle
Tasseau, Olivier
Fares, Fares
Jaber, Nada
Lesot, Philippe
Hachem, Ali
Grée, René
author_sort El Dine, Assaad Nasr
collection PubMed
description Starting from easily accessible gem-difluoropropargylic derivatives, a DBU-mediated isomerisation affords enones in fair yields with a gem-difluoroalkyl chain. These derivatives were used to prepare pyrazolines and pyrrolines with the desired gem-difluoroalkyl side chain by cyclocondensations in good yields and with excellent stereoselectivity. A one-pot process was also successfully developed for these sequential reactions. By carrying out various types of Pd-catalyzed coupling reactions for compounds with a p-bromophenyl substituent a route to focused chemical libraries was demonstrated.
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spelling pubmed-38175752013-11-07 Synthesis of enones, pyrazolines and pyrrolines with gem-difluoroalkyl side chains El Dine, Assaad Nasr Khalaf, Ali Grée, Danielle Tasseau, Olivier Fares, Fares Jaber, Nada Lesot, Philippe Hachem, Ali Grée, René Beilstein J Org Chem Letter Starting from easily accessible gem-difluoropropargylic derivatives, a DBU-mediated isomerisation affords enones in fair yields with a gem-difluoroalkyl chain. These derivatives were used to prepare pyrazolines and pyrrolines with the desired gem-difluoroalkyl side chain by cyclocondensations in good yields and with excellent stereoselectivity. A one-pot process was also successfully developed for these sequential reactions. By carrying out various types of Pd-catalyzed coupling reactions for compounds with a p-bromophenyl substituent a route to focused chemical libraries was demonstrated. Beilstein-Institut 2013-09-26 /pmc/articles/PMC3817575/ /pubmed/24204405 http://dx.doi.org/10.3762/bjoc.9.230 Text en Copyright © 2013, El Dine et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
El Dine, Assaad Nasr
Khalaf, Ali
Grée, Danielle
Tasseau, Olivier
Fares, Fares
Jaber, Nada
Lesot, Philippe
Hachem, Ali
Grée, René
Synthesis of enones, pyrazolines and pyrrolines with gem-difluoroalkyl side chains
title Synthesis of enones, pyrazolines and pyrrolines with gem-difluoroalkyl side chains
title_full Synthesis of enones, pyrazolines and pyrrolines with gem-difluoroalkyl side chains
title_fullStr Synthesis of enones, pyrazolines and pyrrolines with gem-difluoroalkyl side chains
title_full_unstemmed Synthesis of enones, pyrazolines and pyrrolines with gem-difluoroalkyl side chains
title_short Synthesis of enones, pyrazolines and pyrrolines with gem-difluoroalkyl side chains
title_sort synthesis of enones, pyrazolines and pyrrolines with gem-difluoroalkyl side chains
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817575/
https://www.ncbi.nlm.nih.gov/pubmed/24204405
http://dx.doi.org/10.3762/bjoc.9.230
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