Stereocontrolled synthesis of the histrionicotoxin ring system
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference23 articles.
1. Simple total synthesis of (+-)-perhydrohistrionicotoxin
2. Synthetic studies on histrionicotoxins. I. Stereocontrolled synthesis of (+-)-perhydrohistrionicotoxin
3. Syntheses of 1-Azaspiro-[5.5]undecanes: Stereoselective Syntheses of Perhydro- and Octahydrohistrionicotoxin
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1. Synthetic approaches towards alkaloids bearing α-tertiary amines;Natural Product Reports;2016
2. 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
3. Thirty-five years of synthetic studies directed towards the histrionicotoxin family of alkaloids;Natural Product Reports;2007
4. Iodine-Mediated Cyclization of (4R,5R)-4,5-Diamino-N,N′-bis[(1S)-1-phenylethyl]-1,7-octadiene - A Stereoselective Route to 2,5-Diazabicyclo[2.2.1]heptanes;European Journal of Organic Chemistry;2005-09
5. Intramolecular Nucleophilic Substitution at the C-4 Position of Functionalized Oxetanes: A Ring Expansion for the Construction of Various Heterocycles;The Journal of Organic Chemistry;1996-01-01
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