Scalable organocatalytic one pot asymmetric Strecker reaction via camphor sulfonyl functionalized crown-ether-tethered calix[4]arene

Chem Commun (Camb). 2024 Aug 9;60(65):8561-8564. doi: 10.1039/d4cc02674h.

Abstract

In this communication, we designed a highly selective camphor sulfonyl functionalized crown-ether-tethered calix[4]arene-derived organocatalyst for asymmetric Strecker reaction to provide the desired cyano adducts in high yields (∼99.9% yield) and enantioselectivities (up to 99.3% ee). Furthermore, 2 step facile syntheses of the antiplatelet drug (S)-clopidogrel exemplify the potential of this method for the preparation of commercial compounds.