Stereoselective total synthesis of (±)-α-vetispirene, (±)-hinesol, and (±)-β-vetivone based on a Claisen rearrangement
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference65 articles.
1. For the structure of 1, see:
2. Structures of vetivenenes and vetispirenes
3. For total synthesis of (±)-1, see:
4. Synthetic studies on spirovetivanes. II. Stereospecific total synthesis of dl-hinesol, dl-α-vetispirene, and dl-β-vetispirene (dl-β-isovetivenene).
5. Stereospecific synthesis of 6,c-10-dimethyl(r-5-C1)spiro[4.5]dec-6-en-2-one and its conversion into (.+-.)-.alpha.-vetispirene
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