| Literature DB >> 35080408 |
Shuichi Nakamura1,2, Yoichiro Matsuda2, Tsunayoshi Takehara3, Takeyuki Suzuki3.
Abstract
The first enantioselective Pictet-Spengler reaction of acyclic α-ketoesters with tryptamines has been developed. Excellent yields and enantioselectivity were obtained for the reaction using chiral imidazoline-phosphoric acid catalysts. Density functional theory calculations suggested possible transition states that explain the origin of chiral induction. This process provides an efficient route for the synthesis of tetrahydro-β-carboline derivatives.Entities:
Year: 2022 PMID: 35080408 DOI: 10.1021/acs.orglett.1c04316
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005