A computational study of the enantioselective addition of n-BuLi to benzaldehyde in the presence of a chiral lithium N,P amide-Reference-Cited by-同舟云学术

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A computational study of the enantioselective addition of n-BuLi to benzaldehyde in the presence of a chiral lithium N,P amide

Published:2012 Issue:14 Volume:10 Page:2807
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Rönnholm Petra,Gräfenstein Jürgen,Norrby Per-Ola,Hilmersson Göran,Nilsson Lill Sten O.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2012/OB/C2OB06910E

Reference81 articles.

1. Main group organometallics in synthesis

2. Temperature and Solvent Effect on the Nucleophilic Addition ofn-Butyllithium to theN-(Trimethylsilyl)imine of(2S)-Lactal

3. Origin of 1, 3-induction in the addition of alkyl lithium to imines bearing an N-stereogenic center

4. Stereoselectivities of Nucleophilic Additions to Cycloheptanones. Experimental and Theoretical Studies and General Purpose Force Field for the Prediction of Nucleophilic Addition Stereoselectivities

5. Stereoselective Reactions. Part 31: Catalytic Asymmetric Alkylation of Achiral Lithium Enolates Using a Chiral Tetradentate Amine in the Presence of an Achiral Bidentate Amine

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