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Stereoselective generation of vicinal stereogenic quaternary centers by photocycloaddition of 5-methoxy oxazoles to α-keto esters: synthesis of erythro β-hydroxy dimethyl aspartates
Axel G. Griesbeck,Samir Bondock,Johann Lex
Organic & Biomolecular Chemistry Pub Date : 03/17/2004 00:00:00 , DOI:10.1039/B401990C
Abstract

The photocycloaddition of methyl pyruvate and methyl phenylglyoxylate, respectively, to 5-methoxy oxazoles bearing additional substituents at C-2 and C-4 leads to bicyclic oxetanes 2 and 3 with high to moderate (exo) diastereoselectivity that can be easily ring-opened to give bis-quaternary aspartic acid diester derivatives 4 and 5.

Graphical abstract: Stereoselective generation of vicinal stereogenic quaternary centers by photocycloaddition of 5-methoxy oxazoles to α-keto esters: synthesis of erythro β-hydroxy dimethyl aspartates
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