A divergent approach to patchouli sesquiterpenes: Synthesis of 3-oxopatchouli alcohol, 5-oxo-7-hydroxy-13-norcycloseychellene, 6-methoxy-4,12-dehydro-13-norcycloseychellene and patchouli alcohol
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. One-pot annulation to tricyclo[5.3.1.03,8]undecane-2,6-diones by sequential three-fold Michael reactions. A formal synthesis of (±)-seychellene
2. Synthese von (±)-2-Oxo-seychellen und (±)-2-Oxo-4-epi-seychellen
3. Vinyl radical induced Michael additions: Total synthesis of (±)-seychellene
4. Stereocontrolled total synthesis of (±)-norpatchoulenol and two metabolites of patchouli alcohol, (±)-hydroxy patchouli alcohol and the corresponding (±)-carboxylic acid
5. Vinyl sulfone bicycloannulation of cyclohexenones: one-step synthesis of tricyclo[3.2.1.02,7]octan-6-ones
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