Asymmetric synthesis of β-amino alcohol by reductive cross-coupling of planar chiral ferrocenecarboxaldehyde with N-tosyl ferrocenylideneamine, and its application to asymmetric reaction-Reference-Cited by-同舟云学术

Asymmetric synthesis of β-amino alcohol by reductive cross-coupling of planar chiral ferrocenecarboxaldehyde with N-tosyl ferrocenylideneamine, and its application to asymmetric reaction

Published:2004-04 Issue:6 Volume:357 Page:1829-1835
ISSN:0020-1693
Container-title:Inorganica Chimica Acta
language:en
Short-container-title:Inorganica Chimica Acta

Author:

Kimura Takayuki,Shoda Ryohei,Taniguchi Nobukazu,Kamikawa Ken,Uemura Motokazu

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry

Reference75 articles.

1. New Approaches to the Use of Amino Acids as Chiral Building Blocks in Organic Synthesis[New Synthetic Methods(85)]

2. 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis

3. Additions of Organometallic Reagents to CN Bonds: Reactivity and Selectivity

4. Synthesis and Diastereoselective Reactions of N,N-Dibenzylamino Aldehydes and Related Compounds

5. The Synthesis of Vicinal Amino Alcohols

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