Stereocontrolled synthesis of R or S E or Z unsaturated α—amino acids by enantio- and diastereoselective epoxidation of δ-hydroxy allylic phosphine oxides-Reference-Cited by-同舟云学术

Stereocontrolled synthesis of R or S E or Z unsaturated α—amino acids by enantio- and diastereoselective epoxidation of δ-hydroxy allylic phosphine oxides

Published:1993-02 Issue:8 Volume:34 Page:1327-1330
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Clayden Jonathan,Collington Eric W.,Warren Stuart

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference24 articles.

1. Stereocontrolled (, and , ) synthesis of ⊙-hydroxyallylic sulphides

2. Asymmetric epoxidations and kinetic resolutions of δ-hydroxy allylic phosphine oxides

3. Catalytic asymmetric epoxidation and kinetic resolution: modified procedures including in situ derivatization

4. Kinetic resolution of racemic allylic alcohols by enantioselective epoxidation. A route to substances of absolute enantiomeric purity?

5. The synthesis of δ-hydroxy allylic phosphine oxides by palladium(II)-catalysed allylic transposition

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