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An uncatalyzed aldol reaction of thiazolidinediones†
Ajay Chauhan,Kalyan Dhara,Ashwani Kumar Tiwari
Green Chemistry Pub Date : 08/29/2012 00:00:00 , DOI:10.1039/C2GC35819K
Abstract

Thiazolidinediones have been used as aldol donors with aromatic aldehydes “on water” and in DMSO without using any catalyst to give the corresponding β-hydroxy carbonyl compounds in high yield and purity. The p-cyano and p-nitro substituted aldol products undergo syn/anti isomerization via an enolization mechanism providing an “on water” diastereoselectivity switch. Water molecules play a significant role in stabilizing the syn aldol products of pyridine and thiazole containing aldehydes.

Graphical abstract: An uncatalyzed aldol reaction of thiazolidinediones
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