| Literature DB >> 31257897 |
Sifan Yu1, Ruyu Hua1, Xiang Fu1, Gengxin Liu1, Dan Zhang1, Shikun Jia1, Huang Qiu1, Wenhao Hu1.
Abstract
Developing an efficient and highly enantioselective protocol to access homopropargyl amines is of high interest to the synthetic community and also remains a formidable challenge for organic chemists. Here, we present integrated Rh2(OAc)4- and BINOL-derived chiral phosphoric acid cooperatively catalyzed three-component reactions of alkynyldiazoacetates, imines with various nucleophiles including alcohols, indoles, and N,N-disubstituted anilines, affording the corresponding homopropargyl amines containing two vicinal chiral centers in satisfactory yields with high to excellent diastereo- and enantioselectivities.Entities:
Year: 2019 PMID: 31257897 DOI: 10.1021/acs.orglett.9b02139
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005