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Photoredox‐Catalyzed Cyclopropanation of Michael Acceptors
Author(s) -
del Hoyo Ana M.,
García Suero Marcos
Publication year - 2017
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201601604
Subject(s) - cyclopropanation , diiodomethane , chemistry , michael reaction , catalysis , photoredox catalysis , selectivity , organic chemistry , photochemistry , combinatorial chemistry , photocatalysis , surface energy
A new protocol for the catalytic cyclopropanation of α,β‐unsaturated carbonyl compounds with diiodomethane by means of photoredox catalysis has been successfully developed. The transformation is characterized by its mild conditions, functional‐group compatibility, and excellent selectivity profile.
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