Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by (S)-1-Alkyl-2-(arylamino)methylpyrrolidine
Author:
Affiliation:
1. Department of Advanced Materials Chemistry, Graduate School of Engineering, Yokohama National University
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
http://www.journal.csj.jp/doi/pdf/10.1246/bcsj.20120105
Reference48 articles.
1. Enantioselective addition of diethylzinc to benzaldehyde catalyzed by a small amount of chiral 2-amino-1-alcohols
2. Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification
3. Enantioselective addition of organozinc reagents to aldehydes
4. Catalytic Asymmetric Organozinc Additions to Carbonyl Compounds
5. Perhydro-1,3-benzoxazines derived from (−)-8-aminomenthol as ligands for the catalytic enantioselective addition of diethylzinc to aldehydes
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1. Enantioselective addition of diethylzinc to aldehydes catalyzed by 5-cis-substituted proline derivatives;Tetrahedron;2019-01
2. (S)-2-(Anilinomethyl)pyrrolidine;Encyclopedia of Reagents for Organic Synthesis;2016-03-31
3. Carbanions and Electrophilic Aliphatic Substitution;Organic Reaction Mechanisms Series;2015-06-02
4. (S)-2-(Anilinomethyl)pyrrolidine;Encyclopedia of Reagents for Organic Synthesis;2014-10-20
5. Chiral Porous TADDOL-Embedded Organic Polymers for Asymmetric Diethylzinc Addition to Aldehydes;Bulletin of the Chemical Society of Japan;2014-03-15
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