Synthetic studies of taxane carbon framework. A highly efficient eight-membered ring cyclization with complete stereocontrol
- 1 January 1992
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 48 (34) , 6975-6984
- https://doi.org/10.1016/s0040-4020(01)91209-8
Abstract
No abstract availableFunding Information
- Ministry of Education and Science
This publication has 26 references indexed in Scilit:
- TAXANE DITERPENE SYNTHESIS STRATEGIES. A REVIEWOrganic Preparations and Procedures International, 1991
- Stereoselective construction of the taxinine AB system through a novel tandem aldol-Payne rearrangement annulationThe Journal of Organic Chemistry, 1990
- A highly efficient eight-membered-ring cyclization for construction of the taxane carbon frameworkJournal of the American Chemical Society, 1989
- The reaction of 1,1-dimethoxyethylene with bridgehead enones. A direct approach to the taxane skeletonJournal of the Chemical Society, Chemical Communications, 1987
- Inside-outside stereoisomerism: the synthesis of trans-bicyclo[5.3.1]undecane-11-oneJournal of the American Chemical Society, 1986
- Synthesis of a taxane trieneJournal of the American Chemical Society, 1986
- Transition state conformations of a Lewis acid catalyzed Diels-Alder reaction. The low temperature cycloaddition of 1-(1-oxoallyl)-2-(3-isopropenyl-4-methyl-3-pentenyl) benzeneJournal of the American Chemical Society, 1985
- Synthetic studies on the taxane diterpenes. Utility of the intramolecular Diels-Alder reaction for a single-step, stereocontrolled synthesis of a taxane model systemJournal of the American Chemical Society, 1983
- Synthesis of β-chloro, β-bromo, and β-iodo α,β-unsaturated ketonesCanadian Journal of Chemistry, 1982
- The Constituent of the Heartwood of Taxus cuspidata Sieb. et Zucc.CHEMICAL & PHARMACEUTICAL BULLETIN, 1968