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A stepwise retro-imino-ene as a key step in the mechanism of allene formation via the Crabbé acetylene homologation

✍ Scribed by Marta González; Roi Álvarez Rodríguez; Maria Magdalena Cid; Carlos Silva López


Book ID
102878108
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
954 KB
Volume
33
Category
Article
ISSN
0192-8651

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✦ Synopsis


Abstract

The mechanism of the acetylene homologation procedure accidentally discovered and further developed by Crabbé and coworkers is unknown. Kinetic isotope effect (KIE) experiments, however, suggest that an intramolecular hydrogen shift is the key step of the transformation. In this work, we present a computational study of this mechanism. We found that the reaction proceeds via an unexpected stepwise retro‐imino‐ene rearrangement. This mechanism justifies the role of Cu(I) as a reaction catalyst and is also compatible with the KIE experiments reported. © 2012 Wiley Periodicals, Inc.