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Nucleophilic Carbenes: An Incredible Renaissance
Author(s) -
Regitz Manfred
Publication year - 1996
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199607251
Subject(s) - carbene , nucleophile , the renaissance , chemistry , carbon atom , dimer , transition metal carbene complex , molecule , catalysis , combinatorial chemistry , organic chemistry , ring (chemistry) , art history , art
Over thirty years have passed since the pioneering work of H.‐W. Wanzlick on nucleophilic carbenes. A much investigated model is the imidazolidinylidene 1 , which can be generated from dimer 2 and other substrates. The isolation of the stable carbene 3 by A. J. Arduengo III in 1991 sparked incredible developments: addition reactions with increases in the covalency and coordination of the carbene carbon atom dominate the chemistry of such molecules. Recently, Herrmann et al. reported on the use of carbenes as ligands for Pd catalysts.

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