Premium
Tin‐Free Radical Carbonylation: Synthesis of Acylated Oxime Ethers Using Alkyl Allyl Sulfone Precursors, Carbon Monoxide, and Phenylsulfonyl Oxime Ether
Author(s) -
Kim Sangmo,
Lim KyoungChan,
Kim Sunggak,
Ryu Ilhyong
Publication year - 2007
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.200600500
Subject(s) - chemistry , sulfone , oxime , ether , alkyl , carbonylation , carbon monoxide , organic chemistry , tin , medicinal chemistry , polymer chemistry , catalysis
Acylated oxime ethers have been prepared by a three‐component coupling reaction using alkyl allyl sulfone precursors, carbon monoxide, and phenylsulfonyl oxime ether derivatives under tin‐free radical reaction conditions.