A claisen rearrangement strategy for the three-atom ring expansion of cyclic ketones. A total synthesis of (±) precapnelladiene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference36 articles.
1. General approach to annulated 4-cyclooctenones by aliphatic Claisen rearrangement. Stereospecific total synthesis of (.+-.)-precapnelladiene
2. Total synthesis of (.+-.)-poitediol and (.+-.)-dactylol
3. Total synthesis of the marine sesquiterpenes dactylol and africanol. De novo construction of a cyclooctanoid natural product from cycloheptane precursors
4. A general stereocontrolled approach to the 5-8 fused ring system. Application to the total synthesis of the marine natural product (.+-.)-precapnelladiene
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