An efficient preparation of optically active allylic alcohols,2-furyl alcohols and 2-thienyl alcohols by catalytic asymmetric alkylation

1991 ◽  
pp. 25 ◽  
Author(s):  
Masahiko Hayashi ◽  
Toshiyuki Kaneko ◽  
Nobuki Oguni
Keyword(s):  
Optically Active ◽  
Allylic Alcohols ◽  
Asymmetric Alkylation ◽  
Catalytic Asymmetric

Scope and limitations of the catalytic asymmetric rearrangement of epoxides to allylic alcohols using chiral lithium amide bases/lithiated imidazoles

2005 ◽  
Vol 46 (48) ◽  
pp. 8315-8318 ◽  
Author(s):  
Sally J. Oxenford ◽  
Jonathan M. Wright ◽  
Peter O’Brien ◽  
Narendra Panday ◽  
Mark R. Shipton
Keyword(s):  
Allylic Alcohols ◽  
Lithium Amide ◽  
Catalytic Asymmetric

Catalytic, asymmetric alkylation of imines

Tetrahedron ◽  
2007 ◽  
Vol 63 (39) ◽  
pp. 9581-9597 ◽  
Author(s):  
Dana Ferraris∗
Keyword(s):  
Asymmetric Alkylation ◽  
Catalytic Asymmetric

Formation of Optically Active Chromans by Catalytic Asymmetric Tandem Oxa-Michael Addition—Friedel—Crafts Alkylation Reactions.

ChemInform ◽  
2003 ◽  
Vol 34 (39) ◽  
Author(s):  
Hester L. van Lingen ◽  
Wei Zhuang ◽  
Tore Hansen ◽  
Floris P. J. T. Rutjes ◽  
Karl Anker Joergensen
Keyword(s):  
Michael Addition ◽  
Optically Active ◽  
Catalytic Asymmetric ◽  
Alkylation Reactions

Catalytic asymmetric enamine protonation reaction

2018 ◽  
Vol 16 (4) ◽  
pp. 510-520 ◽  
Author(s):  
Niankai Fu ◽  
Long Zhang ◽  
Sanzhong Luo
Keyword(s):  
Carbonyl Compounds ◽  
Optically Active ◽  
Protonation Reaction ◽  
Recent Advances ◽  
Catalytic Asymmetric

Recent advances in catalytic enantioselective enamine protonation for the synthesis of optically active carbonyl compounds are summarized in this review.

Sign in / Sign up

Export Citation Format

Share Document