A Stereoselective Approach to the Azaspiro[5.5]undecane Ring System Using a Conjugate Addition/Dipolar Cycloaddition Cascade: Application to the Total Synthesis of (±)-2,7,8-epi-Perhydrohistrionicotoxin-Reference-Cited by-同舟云学术

A Stereoselective Approach to the Azaspiro[5.5]undecane Ring System Using a Conjugate Addition/Dipolar Cycloaddition Cascade: Application to the Total Synthesis of (±)-2,7,8-epi-Perhydrohistrionicotoxin

Published:2008-08-21 Issue:24 Volume:73 Page:9601-9609
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Wilson Michael S.¹,Padwa Albert¹

Affiliation:

1. Department of Chemistry, Emory University, Atlanta, Georgia 30322

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo801295e

Reference100 articles.

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2. bWitkop, B.; Gössinger, E.InThe Alkaloids;Brossi, A., Ed.Academic Press:New York, 1983; pp139−251.

3. Structure of dihydroisohistrionicotoxin, a unique unsaturated alkaloid and anticholinergic agent

4. Histrionicotoxins: Roentgen-Ray Analysis of the Novel Allenic and Acetylenic Spiroalkaloids Isolated from a Colombian Frog, Dendrobates histrionicus

5. Allenic and Acetylenic Spiropiperidine Alkaloids from the Neotropical Forg,Dendrobates histrionicus

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