Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and Imines by alkenyl-to-allyl 1,4-rhodium(I) migration

A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3-enynes, and imines to give homoallylic sulfamates. The key step is the generation of allylrhodium(I) species by alkenyl-to-allyl 1,4-rhodium(I) migration.

Bibliographic Details
Main Authors: Callingham, Michael, Partridge, Benjamin M., Lewis, William, Lam, Hon Wai
Format: Article
Published: Wiley-VCH Verlag 2017
Subjects:
Online Access:https://eprints.nottingham.ac.uk/47300/
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author Callingham, Michael
Partridge, Benjamin M.
Lewis, William
Lam, Hon Wai
author_facet Callingham, Michael
Partridge, Benjamin M.
Lewis, William
Lam, Hon Wai
author_sort Callingham, Michael
building Nottingham Research Data Repository
collection Online Access
description A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3-enynes, and imines to give homoallylic sulfamates. The key step is the generation of allylrhodium(I) species by alkenyl-to-allyl 1,4-rhodium(I) migration.
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institution University of Nottingham Malaysia Campus
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last_indexed 2025-11-14T20:05:02Z
publishDate 2017
publisher Wiley-VCH Verlag
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spelling nottingham-473002020-05-04T19:22:53Z https://eprints.nottingham.ac.uk/47300/ Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and Imines by alkenyl-to-allyl 1,4-rhodium(I) migration Callingham, Michael Partridge, Benjamin M. Lewis, William Lam, Hon Wai A chiral rhodium complex catalyzes the highly enantioselective coupling of arylboronic acids, 1,3-enynes, and imines to give homoallylic sulfamates. The key step is the generation of allylrhodium(I) species by alkenyl-to-allyl 1,4-rhodium(I) migration. Wiley-VCH Verlag 2017-12-18 Article PeerReviewed Callingham, Michael, Partridge, Benjamin M., Lewis, William and Lam, Hon Wai (2017) Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and Imines by alkenyl-to-allyl 1,4-rhodium(I) migration. Angewandte Chemie International Edition, 56 (51). pp. 16352-16356. ISSN 1521-3773 arylboronic acid; 1 4-migration; imine http://onlinelibrary.wiley.com/doi/10.1002/anie.201709334/abstract doi:10.1002/anie.201709334 doi:10.1002/anie.201709334
spellingShingle arylboronic acid; 1
4-migration; imine
Callingham, Michael
Partridge, Benjamin M.
Lewis, William
Lam, Hon Wai
Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and Imines by alkenyl-to-allyl 1,4-rhodium(I) migration
title Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and Imines by alkenyl-to-allyl 1,4-rhodium(I) migration
title_full Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and Imines by alkenyl-to-allyl 1,4-rhodium(I) migration
title_fullStr Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and Imines by alkenyl-to-allyl 1,4-rhodium(I) migration
title_full_unstemmed Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and Imines by alkenyl-to-allyl 1,4-rhodium(I) migration
title_short Enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and Imines by alkenyl-to-allyl 1,4-rhodium(I) migration
title_sort enantioselective rhodium-catalyzed coupling of arylboronic acids, 1,3-enynes, and imines by alkenyl-to-allyl 1,4-rhodium(i) migration
topic arylboronic acid; 1
4-migration; imine
url https://eprints.nottingham.ac.uk/47300/
https://eprints.nottingham.ac.uk/47300/
https://eprints.nottingham.ac.uk/47300/