Synthesis of sesquiterpene antitumor lactones. 7. Studies directed toward the total synthesis of pentalenolactone. Intramolecular ene reaction.-Reference-Cited by-同舟云学术

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Synthesis of sesquiterpene antitumor lactones. 7. Studies directed toward the total synthesis of pentalenolactone. Intramolecular ene reaction.

Published:1979-01 Issue:23 Volume:20 Page:2115-2118
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Plavac Frank,Heathcock Clayton H.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. The structure and absolute configuration of pentalenolactone (PA 132)

2. Stereospecific total synthesis of dl-pentalenolactone

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1. Carbonylchemie;Organische Synthesemethoden;2023

2. Stereoselective tandem iridium-catalyzed alkene isomerization-cope rearrangement of ω-diene epoxides: efficient access to acyclic 1,6-dicarbonyl compounds;Chemical Science;2021

3. Stereoselective Carbon-Carbon Bond Forming Reactions;Stereoselective Synthesis in Organic Chemistry;1993

4. Cleavage Reactions;Comprehensive Organic Synthesis;1991

5. Ene Reactions with Alkenes as Enophiles;Comprehensive Organic Synthesis;1991

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