Synthesis of β-hydroxyaspartates and β-hydroxymethylserines from N-Boc-(R)-serinal acetonide derived imines through asymmetric [2+2] cycloaddition reaction.-Reference-Cited by-同舟云学术

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Synthesis of β-hydroxyaspartates and β-hydroxymethylserines from N-Boc-(R)-serinal acetonide derived imines through asymmetric [2+2] cycloaddition reaction.

Published:1992-08 Issue:33 Volume:33 Page:4819-4822
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Palomo Claudio,Cabré Francesc,Ontoria Jesús Ma

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference47 articles.

1. New Naturally Occurring Amino Acids

2. α-Amino Acid Synthesis (Tetrahedron Symposium-in-print),1988

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1. Divergent total synthesis of 1,6,8a-tri-epi-castanospermine and 1-deoxy-6,8a-di-epi-castanospermine from substituted azetidin-2-one (β-lactam), involving a cascade sequence of reactions as a key step;Org. Biomol. Chem.;2014

2. ChemInform Abstract: Synthesis of β-Hydroxyaspartates and β-Hydroxymethylserines from N-Boc-(R)-Serinal Acetonide Derived Imines Through Asymmetric (2 + 2)Cycloaddition Reaction.;ChemInform;2010-08-21

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4. Azide-Free Synthesis of Oseltamivir from l-Methionine;Synlett;2009-03-09

5. An efficient formal synthesis of (S)-dapoxetine from enantiopure 3-hydroxy azetidin-2-one;Tetrahedron;2009-03

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