Chiral Sulfoxides in Asymmetric Synthesis: A New Chiral Synthesis of Optically Active 4-Substituted Cyclohexylideneacetic Acid Esters

Synthesis ◽  
1985 ◽  
Vol 1985 (6/7) ◽  
pp. 662-665 ◽  
Author(s):  
Guy Solladié ◽  
Richard Zimmermann ◽  
Richard Bartsch ◽  
Harry Walborsky
Keyword(s):  
Asymmetric Synthesis ◽  
Optically Active ◽  
Chiral Synthesis ◽  
Chiral Sulfoxides ◽  
Acid Esters

Asymmetric Synthesis of Optically Active Sulfinic Acid Esters

2009 ◽  
pp. 31-54 ◽  
Author(s):  
Jzef Drabowicz ◽  
Piotr Kiebasiski ◽  
Dorota Krasowska ◽  
Marian Mikoajczyk
Keyword(s):  
Asymmetric Synthesis ◽  
Optically Active ◽  
Sulfinic Acid ◽  
Acid Esters

ChemInform Abstract: Asymmetric Synthesis of Optically Active Sulfinic Acid Esters

ChemInform ◽  
2009 ◽  
Vol 40 (31) ◽  
Author(s):  
Jozef Drabowicz ◽  
Piotr Kielbasinski ◽  
Dorota Krasowska ◽  
Marian Mikolajczyk
Keyword(s):  
Asymmetric Synthesis ◽  
Optically Active ◽  
Sulfinic Acid ◽  
Acid Esters

Chiral sulfoxides: advances in asymmetric synthesis and problems with the accurate determination of the stereochemical outcome

2018 ◽  
Vol 47 (4) ◽  
pp. 1307-1350 ◽  
Author(s):  
Jianlin Han ◽  
Vadim A. Soloshonok ◽  
Karel D. Klika ◽  
Józef Drabowicz ◽  
Alicja Wzorek
Keyword(s):  
Asymmetric Synthesis ◽  
Accurate Determination ◽  
Optically Active ◽  
The Self ◽  
Chiral Sulfoxides ◽  
Recent Developments

This review covers recent developments for optically active sulfoxide preparations and the problem of accurate determination of the stereochemical outcome due to the self-disproportionation of enantiomers (SDE).

Central–axial–central chirality transfer: asymmetric synthesis of highly substituted indenes bearing a stereogenic quaternary carbon center from optically active propargyl alcohols

2015 ◽  
Vol 51 (2) ◽  
pp. 380-383 ◽  
Author(s):  
Masahiro Egi ◽  
Kaori Shimizu ◽  
Marin Kamiya ◽  
Yuya Ota ◽  
Shuji Akai
Keyword(s):  
Asymmetric Synthesis ◽  
Optically Active ◽  
Quaternary Carbon ◽  
Chirality Transfer ◽  
Propargyl Alcohols

An asymmetric synthesis of highly substituted indenes has been developed via the central–axial–central chirality transfer from optically active propargyl alcohols.

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