Process for the preparation of aromatically substituted acetic acids
申请人:SAGAMI CHEMICAL RESEARCH CENTER
公开号:EP0011279A1
公开(公告)日:1980-05-28
Aromatically substituted acetic acids are prepared by the reaction of an aromatically substituted aldehyde with a combination of a trihalomethane and an alkanethiol, and by the reaction of an alcohol derivative (2,2,2-trihalo-1-arylethanol) with an alkanethiol, in the presence of a base in a mixed medium of water and an aprotic polar solvent.
Copper(I)-Promoted Synthesis of Chloromethyl Ketones from Trichloromethyl Carbinols
作者:Ram N. Ram、T. P. Manoj
DOI:10.1021/jo8007644
日期:2008.7.1
Reaction of several trichloromethyl carbinols with 2 equiv of CuCl/bpy in refluxing DCE for 3 h afforded chloromethyl ketones in excellent yield by 1,2-H shift in the copper-chlorocarbenoid intermediate.
β-(Carbonatoxy)alkyl radicals: a new subset of β-(ester)alkyl radical fragmentation during copper(I)-mediated synthesis of 1,1-dichloro-1-alkenes
作者:Ram N. Ram、Ram K. Tittal
DOI:10.1016/j.tetlet.2014.05.097
日期:2014.7
A new subset of β-(ester)alkyl radicals is presented. It is the first study on the chemistry of β-(alkoxycarbonyloxy)alkyl radicals that fill the gap in the spectrum of the migrating groups in β-(ester)alkyl radical reactions. The change from less nucleofugal (acetate) group to the more nucleofugal (carbonate) group in the spectrum of the migrating group changed the reaction path from rearrangement