| Literature DB >> 23556427 |
George Procopiou1, William Lewis, Gareth Harbottle, Robert A Stockman.
Abstract
The cycloaddition of chiral tert-butanesulfinimines with trimethylenemethane is found to give facile access to methylene-pyrrolidines with good yields and diastereoselectivities. The full scope of the cycloaddition is explored, and a range of transformations of the formed methylenepyrrolidines to give a range of functionalized chiral pyrrolidines is presented.Entities:
Mesh:
Substances:
Year: 2013 PMID: 23556427 DOI: 10.1021/ol400720b
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005