Synthese des (±)-(α)-cuparenons durch hydrocarbonylierende cyclisierung von 1,4-dienen
- 1 January 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (11) , 1131-1132
- https://doi.org/10.1016/s0040-4039(01)91541-2
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Alkylsubstituierte Cyclopentanone durch hydrocarbonylierende Cyclisierung von 1,4‐Pentadiensystemen mit Hilfe von MetallcarbonylenEuropean Journal of Inorganic Chemistry, 1983
- Hybrid Birch-Claisen Methodology for arylation at allylic termini: synthesis of (±)-herberteneTetrahedron Letters, 1982
- Efficient regioselective syntheses of α and β cuparenones. A new approach for the construction of the cyclopentane ringTetrahedron Letters, 1982
- A rapid route to (±)-herbertene, a new sesquiterpeneJournal of the Chemical Society, Chemical Communications, 1982
- Synthesis of dl-3-Hydroxycuparene by a Claisen Rearrangement of Allyl Aryl EtherBulletin of the Chemical Society of Japan, 1982
- An accidental synthesis of (±)-herberteneJournal of the Chemical Society, Chemical Communications, 1982
- Direct geminal dimethylation of ketones using dimethyltitanium dichlorideJournal of the Chemical Society, Chemical Communications, 1981
- A directing effect of neighboring aromatic groups on the regiochemistry of formation and stereochemistry of alkylation and bromination of ketone lithium enolates. Evidence for lithium-arene coordination and dramatic effect of copper(I) in controlling stereochemistry and limiting polyalkylationJournal of the American Chemical Society, 1979
- A single-step synthesis of (±)-α-cuparenoneTetrahedron Letters, 1978