Diastereocontrolled synthesis of functionalized transdecalins via electrocyclic reaction of trienol ethers
- 1 January 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (28) , 4021-4024
- https://doi.org/10.1016/s0040-4039(00)94488-5
Abstract
No abstract availableThis publication has 54 references indexed in Scilit:
- Intramolecular Michael-aldol condensation approach to the construction of advanced intermediates in the synthesis of forskolinThe Journal of Organic Chemistry, 1989
- Chiral .beta.-cyclocitral Schiff base: a combined spectroscopic and theoretical approach to a twisted enimine structureJournal of the American Chemical Society, 1987
- Triene Cyclizations. The Total Synthesis of Pallescensin ASynthetic Communications, 1987
- A SYNTHETIC APPROACH TO THE AB-RING SYSTEM OF FORSKOLINOrganic Preparations and Procedures International, 1986
- New syntheses of (.+-.)-ambrox, (.+-.)-ambra oxide and their stereoisomers.Agricultural and Biological Chemistry, 1986
- Stereoselective acyclic enolate formation via conjugate reduction: correlation with enone conformational preferencesJournal of the American Chemical Society, 1985
- Allenyldiene electrocyclization, a stereospecific tandem center-axis-center chirality transfer: synthesis of drimatrienes and related trans-decalinsJournal of the American Chemical Society, 1985
- Syntheses of the insect antifeedant (.+-.)-cinnamodial and the drimane sesquiterpenoids (.+-.)-isodrimenin and (.+-.)-fragrolideThe Journal of Organic Chemistry, 1985
- An intramolecular Diels–Alder strategy to forskolinJournal of the Chemical Society, Chemical Communications, 1985
- An intramolecular Diels–Alder approach to forskolinJournal of the Chemical Society, Chemical Communications, 1984