Selective reduction of the carbonyl group in organomercurials. A facile method for the protection-deprotection of the mercurio group and a new route to annulated lactones-Reference-Cited by-同舟云学术

Selective reduction of the carbonyl group in organomercurials. A facile method for the protection-deprotection of the mercurio group and a new route to annulated lactones

Published:1996-07 Issue:31 Volume:37 Page:5585-5588
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kočovský Pavel,Dunn Victoria,Grech Jason M.,Šrogl Jiří,Mitchell William L.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. Organomercury Compounds in Organic Synthesis;Larock,1985

2. Solvomercuration - Demercuration Reactions in Organic Synthesis;Larock,1986

3. Intramolecular alkoxymercuration of olefins and stabilization of the resulting organomercurials

4. Radicals in Organic Synthesis: Formation of Carbon-Carbon Bonds;Giese,1986

5. Mercury(II)-mediated opening of cyclopropanes. Effects of proximate internal nucleophiles on stereo- and regioselectivity

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