Synthesis and determination of the absolute stereochemistry of the enantiomers of adrafinil and modafinil

A Osorio-Lozada, T Prisinzano, HF Olivo

文献索引：Osorio-Lozada, Antonio; Prisinzano, Thomas; Olivo, Horacio F. Tetrahedron Asymmetry, 2004 , vol. 15, # 23 p. 3811 - 3815

全文：HTML全文

被引用次数: 25

摘要

Both enantiomers of modafinil, adrafinil, modafinic acid and ethyl modafinate were prepared from the diastereomers formed by reacting racemic β-sulfinyl carboxylic acid with (4R)- phenyl-thiazolidinethione. The absolute stereochemistry of the sulfoxide group was confirmed via X-ray analysis of one of the thiazolidinethione diastereomers.