Tetrahedron: Asymmetry

New stereospecific synthesis of Tesaglitazar and Navaglitazar precursors

E Brenna, C Fuganti, FG Gatti, F Parmeggiani

Index: Brenna, Elisabetta; Fuganti, Claudio; Gatti, Francesco G.; Parmeggiani, Fabio Tetrahedron Asymmetry, 2009 , vol. 20, # 23 p. 2694 - 2698

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Citation Number: 18

Abstract

A new synthetic route of to pharmaceutical intermediates (S)-1a–b and (S)-14 is reported. The reaction pathway is based on the baker's yeast-mediated reduction of the α-alkoxy cinnamaldehydes 9a–c to give the corresponding (S)-alcohols in good yields and excellent ee.