Rhodium-catalyzed arylation of α-amido sulfones with arylboronic acids in a water–toluene biphasic system
摘要:
An efficient method for the synthesis of N-protected diaryl-methyl-amines was developed through a rhodium-catalyzed arylation of alpha-amido sulfones with arylboronic acids in a water-toluene biphasic system. The use of a base combined with a surfactant played a key role in this biphasic reaction. A diverse range of alpha-branched amine derivatives bearing different functional groups were obtained within 10 min under the present conditions. (C) 2010 Elsevier B. V. All rights reserved.
METHOD FOR TREATMENT OF ISOCYANATE RESIDUE, AND METHOD FOR TREATMENT OF CARBONATE
申请人:Mitsui Chemicals, Inc.
公开号:EP2518044A1
公开(公告)日:2012-10-31
A method for treating an isocyanate residue, which comprises carrying out a thermal decomposition reaction of a carbamate that is produced by the reaction among an amine, urea and/or an N-unsubstituted carbamic acid ester and an alcohol to produce a decomposition solution, separating an isocyanate and the alcohol from the decomposition solution to produce the isocyanate residue, and bringing the isocyanate residue into contact with high-pressure/high-temperature water to decompose the isocyanate residue into an amine; and a method for treating a carbonate, which comprises bringing the carbonate into contact with high-pressure/high-temperature water to decompose the carbonate into an alcohol.