Heck reaction of endocyclic enecarbamates with diazonium salts. Formal enantioselective syntheses of alkaloids (−)-codonopsine and (−)-codonopsinine, and the synthesis of a new C-aryl azasugar-Reference-Cited by-同舟云学术

Heck reaction of endocyclic enecarbamates with diazonium salts. Formal enantioselective syntheses of alkaloids (−)-codonopsine and (−)-codonopsinine, and the synthesis of a new C-aryl azasugar

Published:1999-03 Issue:11 Volume:40 Page:2083-2086
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Oliveira Denilson F.,Severino Elias A.,Correia Carlos Roque D.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Recent Developments and New Perspectives in the Heck Reaction

2. Differential oxidation of endocyclic enecarbamates. Synthesis of cyclic β-hydroxy-α-amino acids

3. Stereoselective synthesis of conformationally restricted analogues of aspartic and glutamic acids from endocyclic enecarbamates

4. Synthesis and Reactivity of Optically Active Spiroketals by Ring-Expansion of Chromium Carbene Complex-Derived Cyclobutanones

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