A New Asymmetric Synthesis of (S)-Dolaphenine and Its Heteroaromatic Congeners Utilizing (+)-2-Hydroxy-3-pinanone and (−)-3-Hydroxy-2-caranone as Chiral Auxiliaries-Reference-Cited by-同舟云学术

A New Asymmetric Synthesis of (S)-Dolaphenine and Its Heteroaromatic Congeners Utilizing (+)-2-Hydroxy-3-pinanone and (−)-3-Hydroxy-2-caranone as Chiral Auxiliaries

Published:1995-11 Issue:46 Volume:51 Page:12731-12744
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Irako Naoko,Hamada Yasumasa,Shioiri Takayuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference57 articles.

1. Asymmetric synthesis of α-amino-acid derivatives by alkylation of a chiral Schiff base

2. Amino acids and peptides. XXIX. A new efficient asymmetric synthesis of .ALPHA.-amino acid derivatives with recycle of a chiral reagent - asymmetric alkylation of a chiral Schiff base from glycine.

3. Synthese asymetrique d'acides amines α-disubstitues

4. Asymmetric synthesis of (+)-phosphinothricin and (+)-2-amino-4-phosphonobutyric acid

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