| Literature DB >> 33397992 |
Qi Liu1,2, Haibo Xu1,2, Yuling Li1, Yuan Yao3, Xue Zhang1, Yinlong Guo1, Shengming Ma4,5.
Abstract
<span class="Chemical">Aminespan> are a class of compounds of essential importance in organic synthesis, pharmaceuticals and agrochemicals. Due to the importance of chirality in many practical applications of <span class="Chemical">amines, enantioselective syntheses of <span class="Chemical">amines are of high current interest. Here, we wish to report the development of (R,Ra)-N-Nap-Pyrinap and (R,Sa)-N-Nap-Pyrinap ligands working with CuBr to catalyze the enantioselective A3-coupling of terminal alkynes, aldehydes, and amines affording optically active propargylic amines, which are platform molecules for the effective derivatization to different chiral amines. With a catalyst loading as low as 0.1 mol% even in gram scale reactions, this protocol is applied to the late stage modification of some drug molecules with highly sensitive functionalities and the asymmetric synthesis of the tubulin polymerization inhibitor (S)-(-)-N-acetylcolchinol in four steps. Mechanistic studies reveal that, unlike reported catalysts, a monomeric copper(I) complex bearing a single chiral ligand is involved in the enantioselectivity-determining step.Entities:
Year: 2021 PMID: 33397992 DOI: 10.1038/s41467-020-20205-0
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919