A short route to “reverse-prenylated” pyrrolo[2,3-b]indolesvia tandem olefination and claisen rearrangement of 2-(3,3-dimethylallyloxy)indol-3-ones: First total synthesis of flustramine C-Reference-Cited by-同舟云学术

A short route to “reverse-prenylated” pyrrolo[2,3-b]indolesvia tandem olefination and claisen rearrangement of 2-(3,3-dimethylallyloxy)indol-3-ones: First total synthesis of flustramine C

Published:1996-10 Issue:42 Volume:37 Page:7525-7528
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kawasaki Tomomi,Terashima Romi,Sakaguchi Ken-ei,Sekiguchi Hiroko,Sakamoto Masanori

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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2. 5-N-Acetylardeemin, a novel heterocyclic compound which reverses multiple drug resistance in tumor cells. II. Isolation and elucidation of the structure of 5-N-acetylardeemin and two congeners.

3. Amauromine, a new vasodilator Taxonomy, isolation and characterization.

4. Structure of amauromine, a new hypotensive vasodilator produced by sp.

5. Structure of aszonalenin, a new metabolite of

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