| Literature DB >> 17760449 |
Abstract
A nickel-catalyzed [3+2] cycloaddition of cyclopropyl aldimines and enones has been developed. The process provides direct access to trisubstituted cyclopentanes, and the scope exceeds that of the corresponding reactions involving cyclopropyl ketones. A basis for the improved performance of cyclopropyl aldimines compared with cyclopropyl ketones is provided.Entities:
Year: 2007 PMID: 17760449 DOI: 10.1021/ol071376l
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005