Synthesis of Diastereoenriched Oxazolo[5,4‑<i>b</i>]indoles via Catalyst-Free Multicomponent Bicyclizations

A new and highly eco-friendly approach to diverse and functionalized oxazolo­[5,4-b]­indoles with good yield and high diastereoselectivity (up to >99:1) has been disclosed from simple and readily available arylglyoxals with cyclic enaminones and amino acids. These microwave-assisted transformations in environmentally compatible ethanol resulted in continuous multiple bond-forming events including C–C, C–N, and C–O bonds, enabling catalyst-free multicomponent bicyclizations to rapidly build up functional N,O-heterocycles.