Magnesium halide-catalyzed anti-aldol reactions of chiral N-acylthiazolidinethiones.
摘要：
[reaction: see text] Diastereoselective direct aldol reactions of chiral N-acylthiazolidinethiones occur in high yield with preference for the illustrated anti diastereomer. This reaction is catalyzed by 10% MgBr2.OEt2 in the presence of triethylamine and chlorotrimethylsilane. Yields range from 56 to 93% with diastereoselectivity up to 19:1 for a variety of N-acylthiazolidinethiones and unsaturated aldehydes.
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DOI：
10.1021/ol025553o
被引量：
年份：
2002
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