Studies on the stereoselective selenolactonization, hydroxy and methoxy selenenylation of α- and β-hydroxy acids and esters. Synthesis of δ- and γ-lactones-Reference-Cited by-同舟云学术

Studies on the stereoselective selenolactonization, hydroxy and methoxy selenenylation of α- and β-hydroxy acids and esters. Synthesis of δ- and γ-lactones

Published:2003-03 Issue:13 Volume:59 Page:2241-2251
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Aprile Carmela,Gruttadauria Michelangelo,Amato Maria E,D'Anna Francesca,Lo Meo Paolo,Riela Serena,Noto Renato

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. Stereocontrolled cyclofunctionalizations of double bonds through heterocyclic intermediates

2. Organoselenium Chemistry;Beaulieu,1999

3. Stereocontrolled approach to δ- and γ-lactones and 1,3-diols. The role of X− ion in the selenolactonization

4. Stereoselective Synthesis of Substituted Tetrahydropyran Rings via 6-exo and 6-endo Selenoetherification

5. A joint experimental and ab initio study on the reactivity of several hydroxy selenides. Stereoselective synthesis of cis-disubstituted tetrahydrofurans via seleniranium ions

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