Synthetic approach to pentacyclic quassinoids from communic acids, via ambracetal derivatives
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. Approach to the Synthesis of Antitumor Quassinoids from Labdane Diterpenes: An Efficient Synthesis of a Picrasane-Related Intermediate
2. Amber-type odorants from communic acids
3. Ring A Functionalization of Terpenoids by the Unusual Baeyer-Villiger Rearrangement of Aliphatic Aldehydes
4. Highly Diastereoselective Synthesis of Manoyl Oxide Derivatives by TiCl4-Catalyzed Nucleophilic Cleavage of Ambracetal Derivatives
5. Stereoselective Reduction of Bicyclic Ketals. An Efficient Synthesis of (−)-(R,R)-(cis-6-Methyltetrahydropyran-2-yl)acetic Acid, an Enantiomer of Civet Cat Constituent
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2. Synthesis of ent-ambrox® from (−)-nidorellol;Tetrahedron Letters;2012-10
3. Synthesis of Novel 8,14-Secoursane Derivatives: Key Intermediates for the Preparation of Chiral Decalin Synthons from Ursolic Acid;Helvetica Chimica Acta;2012-06
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5. Synthetic studies towards picrasane quassinoids;Tetrahedron;2007-03
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