Synthesis of spiro-sesquiterpenes in the vetivane series via an aza-claisen rearrangement
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Notes- The Chemistry of Isobutenylamines. II. Alkylation with Allylic and Benzyl Halides.
2. Structure and synthesis of .beta.-vetivone
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4. Stereochemical factors in a cationic cyclization reaction. The synthesis of 10-epi-β-vetivone
5. Ueber Camphenilon
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1. A unified, RCM anchored approach to spiro[4.5]decane-based sesquiterpenoids: Collective synthesis of (±)-α & β-vetispirenes, (±)-β-vetivone, (±)-agarospirol and (±)-hinesol;Tetrahedron Letters;2019-06
2. Total syntheses of natural products containing spirocarbocycles;Organic & Biomolecular Chemistry;2015
3. Aza-Claisen Rearrangement;Comprehensive Organic Name Reactions and Reagents;2010-09-15
4. Total Synthesis of Sesquiterpenes, 1970-79;Total Synthesis of Natural Products;2007-02-20
5. Computational Studies on 3-Aza-Cope Rearrangements: Protonation- Induced Switch of Mechanism in the Reaction of Vinylpropargylamine;Chemistry - A European Journal;2002-02-01
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