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A nordehydroabietyl amide-containing chiral diene for rhodium-catalysed asymmetric arylation to nitroolefins

Yes / A highly enantioselective rhodium catalysed asymmetric arylation
(RCAA) of nitroolefins with arylboronic acids is presented using
a newly developed, C1-symmetric, non-covalent interacted,
phellandrene derived, nordehydroabietyl amide-containing chiral
diene under mild conditions. Stereoelectronic effects were
studied, suggesting an activation of the bound substrate through
the secondary amide as a hydrogen-bond donor.

Identiferoai:union.ndltd.org:BRADFORD/oai:bradscholars.brad.ac.uk:10454/17848
Date02 June 2020
CreatorsLi, R., Wen, Z., Wu, Na
Source SetsBradford Scholars
LanguageEnglish
Detected LanguageEnglish
TypeArticle, Accepted manuscript
Rights(c) 2016 RSC. Full-text reproduced in accordance with the publisher's self-archiving policy., Unspecified

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