Stereo- and Regiochemical Divergence in the Substitution of a Lithiated Alk-1-en-3-yn-2-yl Carbamate: Synthesis of Highly Enantioenriched Vinylallenes or Alk-3-en-5-yn-1-ols-Reference-Cited by-同舟云学术

Stereo- and Regiochemical Divergence in the Substitution of a Lithiated Alk-1-en-3-yn-2-yl Carbamate: Synthesis of Highly Enantioenriched Vinylallenes or Alk-3-en-5-yn-1-ols

Published:2007-04-20 Issue:17 Volume:46 Page:3131-3134
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Bou Chedid Roland,Brümmer Michael,Wibbeling Birgit,Fröhlich Roland,Hoppe Dieter

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference55 articles.

1. Hoch enantiomerenangereicherte Keton-Homoenolat-Reagentien durch (−)-Spartein-vermittelteγ-Deprotonierung von achiralen 1-Alkenylcarbamaten

2. Highly Enantiomerically Enriched Ketone Homoenolate Reagents Prepared by (−)-Sparteine-Mediatedγ-Deprotonation of Achiral 1-Alkenyl Carbamates

3. Highly Enantioenriched Homoenolate Reagents by Asymmetric γ-Deprotonation of Achiral 1-Silyl-Substituted 1-Alkenyl Carbamates

4. Asymmetric γ-Deprotonation and Homoaldol Reaction of 1,3-Dien-2-yl Carbamates: Stereo- and Regiochemistry

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