Designing Fluorinated Cinchona Alkaloids for Enantioselective Catalysis: Controlling Internal Rotation by a Fluorine-Ammonium Ion gauche Effect (φNCCF)-Reference-Cited by-同舟云学术

Designing Fluorinated Cinchona Alkaloids for Enantioselective Catalysis: Controlling Internal Rotation by a Fluorine-Ammonium Ion gauche Effect (φNCCF)

Published:2012-01-16 Issue:7 Volume:18 Page:2006-2013
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Tanzer Eva-Maria,Schweizer W. Bernd,Ebert Marc-Olivier,Gilmour Ryan

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference112 articles.

1. Privileged Chiral Catalysts

2. The stereoselective synthesis of .alpha.-amino acids by phase-transfer catalysis

3. A Rational Approach to Catalytic Enantioselective Enolate Alkylation Using a Structurally Rigidified and Defined Chiral Quaternary Ammonium Salt under Phase Transfer Conditions

4. A new class of asymmetric phase-transfer catalysts derived from Cinchona alkaloids — Application in the enantioselective synthesis of α-amino acids

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