Total syntheses of the diterpenoids (−)-kolavenol and (−)-agelasine B
- 1 November 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (46) , 6923-6926
- https://doi.org/10.1016/s0040-4039(00)60896-1
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Large rate accelerations in the stille reaction with tri-2-furylphosphine and triphenylarsine as palladium ligands: mechanistic and synthetic implicationsJournal of the American Chemical Society, 1991
- Use of the Me3Sn function as a readily removable ‘anchoring’ group in the synthesis of enantiomerically pure bicyclic alcohols and ketonesTetrahedron Letters, 1991
- Clean and convenient procedure for converting primary alkyl iodides and .alpha.,.omega.-diiodoalkanes into the corresponding alkyllithium derivatives by treatment with tert-butyllithiumThe Journal of Organic Chemistry, 1990
- Convenient general method for the preparation of primary alkyllithiums by lithium-iodine exchangeThe Journal of Organic Chemistry, 1990
- Asymmetric synthesis of clerodane diterpenoids: total synthesis of (–)-methyl kolavenateJournal of the Chemical Society, Chemical Communications, 1987
- Structures of Agelasines, Diterpenes Having a 9-Methyladeninium Chromophore Isolated from the Okinawan Marine Sponge Agelas nakamurai HoshinoBulletin of the Chemical Society of Japan, 1986
- Dimethylboron bromide and diphenylboron bromide: cleavage of acetals and ketalsThe Journal of Organic Chemistry, 1984
- Agelasine-A, -B, -C and -D, novel bicyclic diterpenoids with a 9-methyladeninium unit possessing inhibitory effects on na,K-atpase from the okinawa sea sponge sp.1)Tetrahedron Letters, 1984
- Higher-isoprenoids—XTetrahedron, 1979
- Novel reagent system for converting a hydroxy-group into an iodo-group in carbohydrates with inversion of configurationJournal of the Chemical Society, Chemical Communications, 1979