A chiral (alkoxy)methyl-substituted silicon group as an auxiliary for the stereoselective cuprate addition to α,β-unsaturated ketones: synthesis of (−)-(R)-phenyl 2-phenylpropyl ketone-Reference-Cited by-同舟云学术

A chiral (alkoxy)methyl-substituted silicon group as an auxiliary for the stereoselective cuprate addition to α,β-unsaturated ketones: synthesis of (−)-(R)-phenyl 2-phenylpropyl ketone

Published:1997-05 Issue:10 Volume:8 Page:1587-1603
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Bratovanov Svestoslav,Bienz Stefan

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference22 articles.

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2. High asymmetric induction during organometallic .beta.-addition to .alpha.,.beta.-ethylenic sulfoxides. Synthesis of optically active .beta.-alkylcarboxylic acids, .beta.-substituted cyclopentanones, and steroidal 11-oxoequilenin methyl ether

3. Diastereoselective conjugate addition to 3-(p-tolylsulphinyl)chromone: a route to chiral 2-substituted chroman-4-ones

4. Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone.

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