Asymmetric synthesis via acetal templates. 3. On the stereochemistry observed in the cyclization of chiral acetals of polyolefinic aldehydes; formation of optically active homoallylic alcohols

1983 ◽  
Vol 105 (7) ◽  
pp. 2088-2089 ◽  
Author(s):  
Paul A. Bartlett ◽  
William S. Johnson ◽  
John D. Elliott
Keyword(s):  
Asymmetric Synthesis ◽  
Optically Active ◽  
Homoallylic Alcohols

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.

Catalytic asymmetric synthesis of homoallylic alcohols

1993 ◽  
Vol 115 (15) ◽  
pp. 7001-7002 ◽  
Author(s):  
Anna Luisa Costa ◽  
Maria Giulia Piazza ◽  
Emilio Tagliavini ◽  
Claudio Trombini ◽  
Achille Umani-Ronchi
Keyword(s):  
Asymmetric Synthesis ◽  
Catalytic Asymmetric Synthesis ◽  
Homoallylic Alcohols ◽  
Catalytic Asymmetric

Asymmetric synthesis of optically active 6-thiaestrogens

2010 ◽  
Vol 91 (7) ◽  
pp. 861-868 ◽  
Author(s):  
W. M. B. Könst ◽  
W. N. Speckamp ◽  
H. O. Houwen ◽  
H. O. Huisman
Keyword(s):  
Asymmetric Synthesis ◽  
Optically Active
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