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Mitsunobu Reactions Catalytic in Phosphine and a Fully Catalytic System

The Mitsunobu reaction is renowned for its mild reaction conditions and broad substrate tolerance, but has limited utility in process chemistry and industrial applications due to poor atom economy and the generation of stoichiometric phosphine oxide and hydrazine by-products that complicate purifica...

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Detalles Bibliográficos
Autores principales: Buonomo, Joseph A, Aldrich, Courtney C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648044/
https://www.ncbi.nlm.nih.gov/pubmed/26347115
http://dx.doi.org/10.1002/anie.201506263
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author Buonomo, Joseph A
Aldrich, Courtney C
author_facet Buonomo, Joseph A
Aldrich, Courtney C
author_sort Buonomo, Joseph A
collection PubMed
description The Mitsunobu reaction is renowned for its mild reaction conditions and broad substrate tolerance, but has limited utility in process chemistry and industrial applications due to poor atom economy and the generation of stoichiometric phosphine oxide and hydrazine by-products that complicate purification. A catalytic Mitsunobu reaction using innocuous reagents to recycle these by-products would overcome both of these shortcomings. Herein we report a protocol that is catalytic in phosphine (1-phenylphospholane) employing phenylsilane to recycle the catalyst. Integration of this phosphine catalytic cycle with Taniguchi’s azocarboxylate catalytic system provided the first fully catalytic Mitsunobu reaction.
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spelling pubmed-46480442015-11-24 Mitsunobu Reactions Catalytic in Phosphine and a Fully Catalytic System Buonomo, Joseph A Aldrich, Courtney C Angew Chem Int Ed Engl Communications The Mitsunobu reaction is renowned for its mild reaction conditions and broad substrate tolerance, but has limited utility in process chemistry and industrial applications due to poor atom economy and the generation of stoichiometric phosphine oxide and hydrazine by-products that complicate purification. A catalytic Mitsunobu reaction using innocuous reagents to recycle these by-products would overcome both of these shortcomings. Herein we report a protocol that is catalytic in phosphine (1-phenylphospholane) employing phenylsilane to recycle the catalyst. Integration of this phosphine catalytic cycle with Taniguchi’s azocarboxylate catalytic system provided the first fully catalytic Mitsunobu reaction. WILEY-VCH Verlag 2015-10-26 2015-08-17 /pmc/articles/PMC4648044/ /pubmed/26347115 http://dx.doi.org/10.1002/anie.201506263 Text en © 2015 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. https://creativecommons.org/licenses/by-nc/4.0/ © 2015 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Buonomo, Joseph A
Aldrich, Courtney C
Mitsunobu Reactions Catalytic in Phosphine and a Fully Catalytic System
title Mitsunobu Reactions Catalytic in Phosphine and a Fully Catalytic System
title_full Mitsunobu Reactions Catalytic in Phosphine and a Fully Catalytic System
title_fullStr Mitsunobu Reactions Catalytic in Phosphine and a Fully Catalytic System
title_full_unstemmed Mitsunobu Reactions Catalytic in Phosphine and a Fully Catalytic System
title_short Mitsunobu Reactions Catalytic in Phosphine and a Fully Catalytic System
title_sort mitsunobu reactions catalytic in phosphine and a fully catalytic system
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648044/
https://www.ncbi.nlm.nih.gov/pubmed/26347115
http://dx.doi.org/10.1002/anie.201506263
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