Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst

The direct substitution of the OH group of stereogenic alcohols are reported rarely in literature. Here, the authors demonstrate direct substitution of both secondary and tertiary alcohols with chirality transfer leading to enantioenriched 5-membered, 6-membered and aryl-fused 6-membered heterocycli...

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Autores principales:	Rahul A. Watile, Anon Bunrit, Jèssica Margalef, Sunisa Akkarasamiyo, Rabia Ayub, Emi Lagerspets, Srijit Biswas, Timo Repo, Joseph S. M. Samec
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2019
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/642177931c6547d3ba77fdf91901c007
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spelling	oai:doaj.org-article:642177931c6547d3ba77fdf91901c0072021-12-02T16:50:59ZIntramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst10.1038/s41467-019-11838-x2041-1723https://doaj.org/article/642177931c6547d3ba77fdf91901c0072019-08-01T00:00:00Zhttps://doi.org/10.1038/s41467-019-11838-xhttps://doaj.org/toc/2041-1723The direct substitution of the OH group of stereogenic alcohols are reported rarely in literature. Here, the authors demonstrate direct substitution of both secondary and tertiary alcohols with chirality transfer leading to enantioenriched 5-membered, 6-membered and aryl-fused 6-membered heterocyclic compounds.Rahul A. WatileAnon BunritJèssica MargalefSunisa AkkarasamiyoRabia AyubEmi LagerspetsSrijit BiswasTimo RepoJoseph S. M. SamecNature PortfolioarticleScienceQENNature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Rahul A. Watile Anon Bunrit Jèssica Margalef Sunisa Akkarasamiyo Rabia Ayub Emi Lagerspets Srijit Biswas Timo Repo Joseph S. M. Samec Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst
description	The direct substitution of the OH group of stereogenic alcohols are reported rarely in literature. Here, the authors demonstrate direct substitution of both secondary and tertiary alcohols with chirality transfer leading to enantioenriched 5-membered, 6-membered and aryl-fused 6-membered heterocyclic compounds.
format	article
author	Rahul A. Watile Anon Bunrit Jèssica Margalef Sunisa Akkarasamiyo Rabia Ayub Emi Lagerspets Srijit Biswas Timo Repo Joseph S. M. Samec
author_facet	Rahul A. Watile Anon Bunrit Jèssica Margalef Sunisa Akkarasamiyo Rabia Ayub Emi Lagerspets Srijit Biswas Timo Repo Joseph S. M. Samec
author_sort	Rahul A. Watile
title	Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst
title_short	Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst
title_full	Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst
title_fullStr	Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst
title_full_unstemmed	Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst
title_sort	intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(iii) catalyst
publisher	Nature Portfolio
publishDate	2019
url	https://doaj.org/article/642177931c6547d3ba77fdf91901c007
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Intramolecular substitutions of secondary and tertiary alcohols with chirality transfer by an iron(III) catalyst

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