A new synthesis of both the enantiomers of 4-amino-3-hydroxybutanoic acid (gabob) and mm2 calculations for rotamers of the intermediate oxazolidin-2-on-Reference-Cited by-同舟云学术

A new synthesis of both the enantiomers of 4-amino-3-hydroxybutanoic acid (gabob) and mm2 calculations for rotamers of the intermediate oxazolidin-2-on

Published:1987-01 Issue:19 Volume:43 Page:4377-4383
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Bongini Alessandro,Cardillo Giuliana,Orena Mario,Porzi Gianni,Sandri Sergio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. An efficient synthesis of (R)-(+)- and (S)-(-)-propranolol from resolved 5-idomethyloxazo-lidin-2-ones

2. Stereo- and regiocontrolled synthesis of methyl N-acetyl-.alpha.-D-sibirosaminide

3. Stereoselective synthesis of the dihydroxyisoleucine constituent of the amanita mushroom toxins

4. Carbonyl participation in the reaction of N-acyl-2-isopropenylpyrrolidines with halogen electrophiles. Stereocontrolled preparation of enantiomerically pure synthons for the synthesis of pumiliotoxin A alkaloids.

5. Halonium-initiated cyclizations of allylic urethanes: stereo- and regioselectivity in functionalizing the olefinic bond

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