z-logo
Premium
Organocatalytic Stereoselective α ‐Formylation of Ketones
Author(s) -
Capdevila Montse Guiteras,
Emer Enrico,
Gualandi Andrea,
Petruzziello Diego,
Grilli Stefano,
Cozzi Pier Giorgio
Publication year - 2012
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.201200122
Subject(s) - formylation , enantioselective synthesis , chemistry , electrophile , organocatalysis , enamine , stereoselectivity , carbene , iodide , organic chemistry , catalysis , ketone
A formal… formyl: N ‐Methylbenzothiazolium iodide, a precursor of carbene and an electrophilic compound, has been shown to reacts with the enamine of ketones in a highly enantioselective formylation reaction.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom