Diastereoselective synthesis of γ-hydroxy-β-amino alcohols, (2S, 3S)- and (2S, 3R)-threoninol and -hydroxyphenylalaninol, from (R)-glycidol via the derived 4-hydroxymethyloxazolidinone-Reference-Cited by-同舟云学术

Diastereoselective synthesis of γ-hydroxy-β-amino alcohols, (2S, 3S)- and (2S, 3R)-threoninol and -hydroxyphenylalaninol, from (R)-glycidol via the derived 4-hydroxymethyloxazolidinone

Published:1994-01 Issue:2 Volume:5 Page:161-164
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Katsumura Shigeo,Yamamoto Noriyoshi,Morita Makiko,Han Qingjun

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference21 articles.

1. A convenient reduction of amino acids and their derivatives

2. Functions of Sphingolipids and Sphingolipid Breakdown Products in Cellular Regulation

3. Stereocontrolled addition to a penaldic acid equivalent: an asymmetric of -β-hydroxy-L-glutamic acid

4. A stereodivergent synthesis of D-erythro-sphingosine and D-threo-sphingosine from L-serine

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