A Stereocontrolled Synthesis of (+)- Rhopaloic Acid A Using a Dioxabicyclo- [3.2.1]octane Chiral Building Block
- 1 January 2003
- journal article
- Published by The Japan Institute of Heterocyclic Chemistry in HETEROCYCLES
- Vol. 59 (2) , 485
- https://doi.org/10.3987/com-02-s70
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Enantio- and Diastereoselective Synthesis of (-)-Semburin and (-)-Isosemburin, Monoterpenes isolated from Swertia japonicaSynlett, 2002
- Preparation and Exploitation of Chiral Building Blocks Having A Dioxabicyclo[3,2,1]octane Framework.Journal of Synthetic Organic Chemistry, Japan, 2002
- Recent applications of olefin metathesis and related reactions in carbohydrate chemistryChemical Communications, 2000
- Lipase-Mediated Preparation of Sugar Building BlocksSynthesis, 1999
- Back to the Sugars: A New Enantio and Diastereocontrolled Route to Hexoses from FurfuralSynthesis, 1999
- Recent advances in olefin metathesis and its application in organic synthesisTetrahedron, 1998
- Stereoselective syntheses of (+)-rhopaloic acid A and (−)-ent- and (±)-rac-rhopaloic acid AJournal of the Chemical Society, Perkin Transactions 1, 1998
- Total synthesis of (±)-rhopaloic acid ATetrahedron Letters, 1997
- Stereoselectivity in the Formation of 2,5-Disubstituted Tetrahydropyrans by Intramolecular Hetero-Michael AdditionHETEROCYCLES, 1997
- Rhopaloic acid A: A novel norsesterterpene from a marine sponge, Rhopaloeides sp., which inhibits gastrulation of starfish embryosTetrahedron Letters, 1996