A stereospecific formal synthesis of clavulones from tricyclo[5.2.1.02,6]decadienone epoxides
- 1 June 1991
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 32 (26) , 3131-3132
- https://doi.org/10.1016/0040-4039(91)80708-e
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Tricyclo[5.2.1.02,6]decadienone epoxides: rigid, highly congested α,β-epoxycyclopentanones with distinctive chemical behavior.Tetrahedron Letters, 1991
- Isomer selectivity in stereocontrolled Payne rearrangement–epoxide cleavage of 2,3-epoxy alcohols in aprotic solvents: application to an enantioselective total synthesis of (+)-exo-brevicominJournal of the Chemical Society, Perkin Transactions 1, 1990
- Enzymic optical resolution and absolute configuration of tricyclo[5.2.1.02,6]decadienonesTetrahedron Letters, 1986
- Total synthesis of clavulonesTetrahedron Letters, 1985
- Synthesis of clavulones (claviridenones)Tetrahedron Letters, 1985
- Total synthesis of (.+-.)-clavulonesJournal of the American Chemical Society, 1984
- 9-Deoxy-delta 9, delta 12-13,14-dihydroprostaglandin D2, a metabolite of prostaglandin D2 formed in human plasma.Proceedings of the National Academy of Sciences, 1984
- Total synthesis of marine prostanoids clavulonesTetrahedron Letters, 1984
- Absolute stereochemistry of new prostanoids clavulone I, II and III, from Quoy and GaimardTetrahedron Letters, 1983
- Absolute stereostructures of claviridenone-A, -B, -C, and -D four prostanoids from the Okinawan soft coral Clavularia viridis.CHEMICAL & PHARMACEUTICAL BULLETIN, 1983