Journal of the American Chemical Society 2005-05-25

Catalytic enantioselective thioester aldol reactions that are compatible with protic functional groups.

Derek Magdziak, Gojko Lalic, Hong Myung Lee, Kevin C Fortner, Allen D Aloise, Matthew D Shair

Index: J. Am. Chem. Soc. 127 , 7284, (2005)

Full Text: HTML

Abstract

This communication reports highly enantioselective and diastereoselective methyl malonic acid half thioester (MeMAHT) aldol reactions that are compatible with protic functional groups and enolizable aldehydes, affording syn S-phenyl thiopropionates.


Related Compounds

  • 3-Hydroxy-4-nitrob...

Related Articles:

Tyrphostin AG126 exerts neuroprotection in CNS inflammation by a dual mechanism.

2015-06-01

[Glia 63(6) , 1083-99, (2015)]

Characterization of a transient intermediate formed in the liver alcohol dehydrogenase catalyzed reduction of 3-hydroxy-4-nitrobenzaldehyde.

1987-06-02

[Biochemistry 26(11) , 3058-67, (1987)]

More Articles...