A short and stereoselective synthesis of perhydrohistrionicotoxin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Allenic and Acetylenic Spiropiperidine Alkaloids from the Neotropical Forg,Dendrobates histrionicus
2. Synthetic studies on histrionicotoxins. I. Stereocontrolled synthesis of (+-)-perhydrohistrionicotoxin
3. Synthetic studies on histrionicotoxins. II. Practical synthetic route to (+-)-perhydro- and (+-)-octahydrohistrionicotoxin
4. Simple total synthesis of (+-)-perhydrohistrionicotoxin
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1. 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;The Journal of Organic Chemistry;2008-08-21
2. Thirty-five years of synthetic studies directed towards the histrionicotoxin family of alkaloids;Natural Product Reports;2007
3. Formal Synthesis of (−)-Perhydrohistrionicotoxin via Cyclic Amino Acid Ester−Enolate Claisen Rearrangement and Ring-Closing Metathesis;The Journal of Organic Chemistry;2005-06-01
4. Development of New Synthetic Methods and Its Application to Total Synthesis of Nitrogen-Containing Bioactive Natural Products;Chemical and Pharmaceutical Bulletin;2005
5. Cyclizations of N-Acyliminium Ions;Chemical Reviews;2004-03-01
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