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Decarboxylative Arylation of α,β‐Unsaturated Carboxylic Acids Using Aryl Triazenes by Copper/Ionic Liquid Combination in PEG‐400
Author(s) -
Kumar Saurabh,
Kumar Pandey Anand,
Singh Rahul,
Nand Singh Krishna
Publication year - 2018
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201800930
Subject(s) - chemistry , aryl , stereoselectivity , substrate (aquarium) , yield (engineering) , copper , functional group , ionic liquid , cinnamic acid , combinatorial chemistry , decarboxylation , catalysis , peg ratio , organic chemistry , alkyl , oceanography , materials science , polymer , finance , economics , metallurgy , geology
A practical method for the construction of stilbene derivatives has been developed via catalytic cross‐coupling of cinnamic acids with aryl triazenes. The methodology offers high stereoselectivity and is endowed with broad substrate scope, high yield, and significant functional group tolerance.