Palladium‐Catalyzed Insertion of α‐Diazoesters into Vinyl Halides To Generate α,β‐Unsaturated γ‐Amino Esters
2009; Wiley; Volume: 48; Issue: 20 Linguagem: Inglês
10.1002/anie.200805483
ISSN1521-3773
AutoresRomas Kudirka, Sean K. J. Devine, Christopher S. Adams, David L. Van Vranken,
Tópico(s)Catalytic Cross-Coupling Reactions
ResumoAs easy as 1, 2, 3: A palladium-catalyzed three-component coupling generates alpha,beta-unsaturated gamma-amino acids in a single step (see scheme). The reaction is believed to involve migration of a vinyl substituent to a highly electrophilic palladium carbene. Unlike previous synthetic approaches, this synthesis provides access to gamma-amino acids with non-natural side chains.
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