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Enantioselective Intramolecular 1,5‐Hydride Transfer/Cyclization through the Direct Functionalization of C(sp 3 )‐H Bonds Adjacent to a Heteroatom: From Nitrogen to Oxygen
Author(s) -
Wang Min
Publication year - 2013
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201200692
Subject(s) - enantioselective synthesis , intramolecular force , chemistry , heteroatom , surface modification , hydride , nitrogen , photochemistry , oxygen , medicinal chemistry , catalysis , stereochemistry , organic chemistry , ring (chemistry) , hydrogen
Direct and effective: the asymmetric catalytic 1,5‐hydride transfer/cyclization, internal redox process, has recently been reported. This transformation is an effective method to functionalization of sp 3 ‐CH bond adjacent to heteroatom.
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