Asymmetric Deprotonation using s-BuLi or i-PrLi and Chiral Diamines in THF: The Diamine Matters-Reference-Cited by-同舟云学术

Asymmetric Deprotonation using s-BuLi or i-PrLi and Chiral Diamines in THF: The Diamine Matters

Published:2010-10-11 Issue:43 Volume:132 Page:15445-15450
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Carbone Giorgio¹,O’Brien Peter¹,Hilmersson Göran¹

Affiliation:

1. Department of Chemistry, University of York, Heslington, York YO10 5DD, U.K., and Department of Chemistry, University of Gothenburg, SE-412 96 Göteborg, Sweden

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja107672h

Reference39 articles.

1. Generation of Enantiomerically Enriched Lithium Indenides by Means of(–)-Sparteine: Structure, Stereoselective Substitution, and Solvent Effects

2. Asymmetric Deprotonation by BuLi/(−)-Sparteine: Convenient and Highly Enantioselective Syntheses of (S)-2-Aryl-Boc-Pyrrolidines

3. (−)-Sparteine-Mediated α-Lithiation of N-Boc-N-(p-methoxyphenyl)benzylamine: Enantioselective Syntheses of (S) and (R) Mono- and Disubstituted N-Boc-benzylamines

4. Asymmetric Deprotonations: Lithiation of N-(tert-Butoxycarbonyl)indoline with sec-Butyllithium/(−)-Sparteine

5. Chiral base promoted enantioselective rearrangement of organophosphorus epoxides

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