Tetrahedron letters

Enantiospecific synthesis of optically pure (3S)-hydroxy esters by the stereocontrolled yeast reduction of α-sulfenyl-β-ketoesters

T Fujisawa, T Itoh, T Sato

Index: Tetrahedron Letters, , vol. 25, # 44 p. 5083 - 5086

Full Text: HTML

Citation Number: 83

Abstract

... Content. Citation Only; Citation and Abstract; Advanced search. JavaScript is disabled on your browser. Please enable JavaScript to use all the features on this page. Tetrahedron Letters. Volume 25, Issue 44, 1984, Pages 5083–5086. Cover image Cover image. ...

Stereocontrol by introduction of a sulfur functional group i...

[Tetrahedron Letters, , vol. 27, # 44 p. 5405 - 5408]

The product of Baker's yeast reduction of ethyl 2-chloro-3-o...

[Hamdani, Mourad; Jeso, Bernard De; Deleuze, Herve; Saux, Annie; Maillard, Bernard Tetrahedron: Asymmetry, 1993 , vol. 4, # 6 p. 1233 - 1236]

Practical enzymatic route to optically active 3-hydroxyamide...

[Tetrahedron: Asymmetry, , vol. 4, # 10 p. 2199 - 2210]

Efficient large scale stereoinversion of (R)-ethyl 3-hydroxy...

[Tetrahedron Asymmetry, , vol. 15, # 5 p. 821 - 825]

Diastereoselective route to (2R, 5S)-and (2S, 5S)-2-methyl-1...

[Zarbin, Paulo H. G.; De Oliveira, Alfredo R. M.; Delay, Carlos E. Tetrahedron Letters, 2003 , vol. 44, # 36 p. 6849 - 6851]