Release Time:2019-03-09 Hits:
Indexed by: Journal Article
Date of Publication: 2010-06-18
Journal: ORGANIC LETTERS
Included Journals: Scopus、PubMed、SCIE
Volume: 12
Issue: 12
Page Number: 2726-2729
ISSN: 1523-7060
Abstract: A highly efficient and regioselective allylation reaction of amines and active methylene compounds directly using allylic alcohols under mild conditions catalyzed by the novel cubane-type sulfido [(Cp*Mo)(3)(mu(3)center dot S)(4)Pd(eta(3)-allyl)][PF6](2) clusters has been developed. A variety of allylic alcohols and nucleophiles including amines and active methylene compounds are investigated, and in the case of allylic alcohols bearing substituents at either the alpha- or gamma-position only linear products are obtained.