Tetrahedron letters

Stereocontrol by introduction of a sulfur functional group in the asymmetric reduction of β-ketoesters with baker's yeast; preparation of optically pure 3s- …

T Itoh, Y Yonekawa, T Sato, T Fujisawa

Index: Tetrahedron Letters, , vol. 27, # 44 p. 5405 - 5408

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Citation Number: 57

Abstract

... Downloading zip file containing 3 articles... JavaScript is disabled on your browser. Please enable JavaScript to use all the features on this page. Tetrahedron Letters. Volume 27, Issue 44, 1986, Pages 5405–5408. Cover image Cover image. ...

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]

New class of chiral diphosphine ligands for highly efficient...

[Benincori, Tiziana; Brenna, Elisabetta; Sannicolo, Franco; Trimarco, Licia; Antognazza, Patrizia; et al. Journal of Organic Chemistry, 1996 , vol. 61, # 18 p. 6244 - 6251]