A single-step synthesis of (±)-α-cuparenone
- 1 January 1978
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 19 (11) , 993-994
- https://doi.org/10.1016/s0040-4039(01)85433-2
Abstract
No abstract availableFunding Information
- Ministry of Education
This publication has 8 references indexed in Scilit:
- A surprising effect of a 3-phenyl group on the stereochemistry of cyclopentanone enolate alkylation. Highly stereoselective organocopper 2,3-dialkylation of 2-cyclopentenones. Synthesis of sesquiterpene hydrocarbon (±)-laureneTetrahedron Letters, 1977
- Carbon-carbon bond formations promoted by transition metal carbonyls. 15. Regioselectivity of the iron carbonyl promoted cyclocoupling reaction of .alpha.,.alpha.'-Dibromo ketones with olefins and dienesJournal of the American Chemical Society, 1977
- Stereochemistry of the electrophilic olefinic substitution of 2-oxyallyl--iron (II). Species. Inspection of the conformation of the zwitterionic intermediates1Tetrahedron Letters, 1976
- Carbon-carbon bond formations promoted by transition metal carbonyls. XI. Method for the generation of a synthetic equivalent of unsubstituted oxyallyl via the bromo ketone-iron carbonyl reaction. New route to thujaplicinsThe Journal of Organic Chemistry, 1975
- Microwave spectrum, substitutional structure, and Stark and Zeeman effects in cyclopropenoneJournal of the American Chemical Society, 1973
- Carbon-carbon bond formations promoted by transition metal carbonyls. III. Mechanistic aspects of the reaction of .alpha.,.alpha.1-dibromo ketones and iron carbonyl. Reductive rearrangements of dibromo ketonesJournal of the American Chemical Society, 1972
- Ketones from “mayur pankhi” : some new cuparene-based sesquiterpenoidsTetrahedron Letters, 1964
- 303. The total synthesis of (±)-cupareneJournal of the Chemical Society, 1962