Reversal Diastereofacial Selectivity in then-Butyllithium Addition toO-ProtectedN-Trimethylsilylimines of (2S)-Lactal: Enthalpic versus Entropic Contributions-Reference-Cited by-同舟云学术

Reversal Diastereofacial Selectivity in then-Butyllithium Addition toO-ProtectedN-Trimethylsilylimines of (2S)-Lactal: Enthalpic versus Entropic Contributions

Published:1999-01 Issue:1 Volume:1999 Page:61-65
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Cainelli Gianfranco,Giacomini Daria,Galletti Paola

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference44 articles.

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4. For a review on classical conformational models: [4a] , , Stereochemistry of Organic Compounds; Wiley: New York, 1994, p. 875. For recent theoretical studies see:

5. A Theoretical Study of Addition of Organomagnesium Reagents to Chiral α-Alkoxy Carbonyl Compounds

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