Highly Stereoselective Synthesis of Trifluoromethylated Compounds via Ester-Enolate [2,3]-Wittig and [3,3]-Ireland−Claisen Rearrangements

1997 ◽  
Vol 62 (1) ◽  
pp. 137-150 ◽  
Author(s):  
Tsutomu Konno ◽  
Hideki Umetani ◽  
Tomoya Kitazume
Keyword(s):  
Stereoselective Synthesis ◽  
Claisen Rearrangements ◽  
Ester Enolate

1,4-Chirality transfer via the ester enolate Claisen rearrangements in the preparation of (25R)- and (25S)-cholestenoic acids

Steroids ◽  
2013 ◽  
Vol 78 (7) ◽  
pp. 683-692 ◽  
Author(s):  
Yurii V. Ermolovich ◽  
Vladimir N. Zhabinskii ◽  
Vladimir A. Khripach
Keyword(s):  
Chirality Transfer ◽  
Claisen Rearrangements ◽  
Ester Enolate

ChemInform Abstract: Stereoselective Synthesis of (.+-.)-4-epi-Acetomycin by the Ester Enolate Carroll Rearrangement.

ChemInform ◽  
2010 ◽  
Vol 23 (27) ◽  
pp. no-no
Author(s):  
A. M. ECHAVARREN ◽  
J. DE MENDOZA ◽  
P. PRADOS ◽  
A. ZAPATA
Keyword(s):  
Stereoselective Synthesis ◽  
Ester Enolate
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