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Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α‐Oxy‐ and α‐Thio‐Substituted Organolithium Species

Nonstabilized α‐O‐substituted tertiary organolithium species are difficult to generate, and the α‐S‐substituted analogues are configurationally unstable. We now report that they can both be generated easily and trapped with a range of electrophiles with high enantioselectivity, providing ready acces...

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Detalles Bibliográficos
Autores principales: Pulis, Alexander P., Varela, Ana, Citti, Cinzia, Songara, Pradip, Leonori, Daniele, Aggarwal, Varinder K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601220/
https://www.ncbi.nlm.nih.gov/pubmed/28783238
http://dx.doi.org/10.1002/anie.201706722
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author Pulis, Alexander P.
Varela, Ana
Citti, Cinzia
Songara, Pradip
Leonori, Daniele
Aggarwal, Varinder K.
author_facet Pulis, Alexander P.
Varela, Ana
Citti, Cinzia
Songara, Pradip
Leonori, Daniele
Aggarwal, Varinder K.
author_sort Pulis, Alexander P.
collection PubMed
description Nonstabilized α‐O‐substituted tertiary organolithium species are difficult to generate, and the α‐S‐substituted analogues are configurationally unstable. We now report that they can both be generated easily and trapped with a range of electrophiles with high enantioselectivity, providing ready access to a range of enantioenriched tertiary alcohols and thiols. The configurational stability of the α‐S‐organolithium species was enhanced by using a less coordinating solvent and short reaction times.
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spelling pubmed-56012202017-10-03 Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α‐Oxy‐ and α‐Thio‐Substituted Organolithium Species Pulis, Alexander P. Varela, Ana Citti, Cinzia Songara, Pradip Leonori, Daniele Aggarwal, Varinder K. Angew Chem Int Ed Engl Communications Nonstabilized α‐O‐substituted tertiary organolithium species are difficult to generate, and the α‐S‐substituted analogues are configurationally unstable. We now report that they can both be generated easily and trapped with a range of electrophiles with high enantioselectivity, providing ready access to a range of enantioenriched tertiary alcohols and thiols. The configurational stability of the α‐S‐organolithium species was enhanced by using a less coordinating solvent and short reaction times. John Wiley and Sons Inc. 2017-08-07 2017-08-28 /pmc/articles/PMC5601220/ /pubmed/28783238 http://dx.doi.org/10.1002/anie.201706722 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Pulis, Alexander P.
Varela, Ana
Citti, Cinzia
Songara, Pradip
Leonori, Daniele
Aggarwal, Varinder K.
Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α‐Oxy‐ and α‐Thio‐Substituted Organolithium Species
title Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α‐Oxy‐ and α‐Thio‐Substituted Organolithium Species
title_full Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α‐Oxy‐ and α‐Thio‐Substituted Organolithium Species
title_fullStr Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α‐Oxy‐ and α‐Thio‐Substituted Organolithium Species
title_full_unstemmed Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α‐Oxy‐ and α‐Thio‐Substituted Organolithium Species
title_short Asymmetric Synthesis of Tertiary Alcohols and Thiols via Nonstabilized Tertiary α‐Oxy‐ and α‐Thio‐Substituted Organolithium Species
title_sort asymmetric synthesis of tertiary alcohols and thiols via nonstabilized tertiary α‐oxy‐ and α‐thio‐substituted organolithium species
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5601220/
https://www.ncbi.nlm.nih.gov/pubmed/28783238
http://dx.doi.org/10.1002/anie.201706722
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