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Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction

Unactivated acyclic internal aliphatic olefins are often found to be unreactive in conventional alkenylation reactions. To address this problem, a cobalt catalyzed allylic selective dehydrogenative Heck reaction with internal aliphatic olefins has been developed. The method is highly regio- and ster...

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Autores principales: Maity, Soham, Dolui, Pravas, Kancherla, Rajesh, Maiti, Debabrata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618772/
https://www.ncbi.nlm.nih.gov/pubmed/28970904
http://dx.doi.org/10.1039/c7sc01204g
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author Maity, Soham
Dolui, Pravas
Kancherla, Rajesh
Maiti, Debabrata
author_facet Maity, Soham
Dolui, Pravas
Kancherla, Rajesh
Maiti, Debabrata
author_sort Maity, Soham
collection PubMed
description Unactivated acyclic internal aliphatic olefins are often found to be unreactive in conventional alkenylation reactions. To address this problem, a cobalt catalyzed allylic selective dehydrogenative Heck reaction with internal aliphatic olefins has been developed. The method is highly regio- and stereoselective, the conditions are mild and a wide variety of functional groups can be tolerated. Remarkably, both internal and terminal aliphatic olefins can be employed, thereby significantly expanding the scope of alkenylation chemistry with aliphatic olefins.
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spelling pubmed-56187722017-10-02 Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction Maity, Soham Dolui, Pravas Kancherla, Rajesh Maiti, Debabrata Chem Sci Chemistry Unactivated acyclic internal aliphatic olefins are often found to be unreactive in conventional alkenylation reactions. To address this problem, a cobalt catalyzed allylic selective dehydrogenative Heck reaction with internal aliphatic olefins has been developed. The method is highly regio- and stereoselective, the conditions are mild and a wide variety of functional groups can be tolerated. Remarkably, both internal and terminal aliphatic olefins can be employed, thereby significantly expanding the scope of alkenylation chemistry with aliphatic olefins. Royal Society of Chemistry 2017-07-01 2017-05-16 /pmc/articles/PMC5618772/ /pubmed/28970904 http://dx.doi.org/10.1039/c7sc01204g Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Maity, Soham
Dolui, Pravas
Kancherla, Rajesh
Maiti, Debabrata
Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction
title Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction
title_full Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction
title_fullStr Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction
title_full_unstemmed Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction
title_short Introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative Heck reaction
title_sort introducing unactivated acyclic internal aliphatic olefins into a cobalt catalyzed allylic selective dehydrogenative heck reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618772/
https://www.ncbi.nlm.nih.gov/pubmed/28970904
http://dx.doi.org/10.1039/c7sc01204g
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