| Literature DB >> 30693781 |
Pengfei Zhou1, Xiaohua Liu1, Wangbin Wu1, Chaoran Xu1, Xiaoming Feng1.
Abstract
A catalytic regio- and enantioselective haloazidation reaction with a chiral iron(II) complex catalyst under mild reaction conditions was reported. By this approach, the stereoselective α-halo-β-azido difunctionalization of both α,β-unsaturated amides and α,β-unsaturated esters was achieved. This method enabled the construction of a broad spectrum of valuable functionalized amides and esters, including enantiomerically enriched β-azido amides, aziridine amides, α-amino amide derivatives, β-triazole amides, functionalized peptide derivatives, and α-halo-β-azido-substituted esters.Entities:
Year: 2019 PMID: 30693781 DOI: 10.1021/acs.orglett.9b00110
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005