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 (±)-laurene
- 31 December 1977
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 18 (37) , 3215-3218
- https://doi.org/10.1016/s0040-4039(01)83200-7
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
- Simple total synthesis of prostaglandins from 4-cumyloxy-2-cyclopentenoneJournal of the American Chemical Society, 1975
- Regiospecific Intramolecular Aldol Condensation Induced by Conjugate Addition of lithium dimethylcuprate to ζ‐Oxo‐α, β‐enones preliminary communication [1]Helvetica Chimica Acta, 1975
- Regiospecific alkylation of enolate ions in liquid ammonia-tetrahydrofuranThe Journal of Organic Chemistry, 1975
- Regiospecific acylation of organocopper enolates: a new synthesis of 7-oxoprostaglandinsTetrahedron Letters, 1975
- Alkylation of enolate ions generated regiospecifically via organocopper reactions. Synthesis of decalin sesquiterpene valerane and of prostaglandin model systemsJournal of the American Chemical Society, 1975
- Conjugate addition-annelation. Highly regiospecific and stereospecific synthesis of polycyclic ketonesJournal of the American Chemical Society, 1973
- Synthesis of substituted hydroazulenesThe Journal of Organic Chemistry, 1973
- Cationic benzene and olefin complexes of copper(I) trifluoromethanesulphonateJournal of the Chemical Society, Chemical Communications, 1972
- .pi. Complexation in ion pair bonding. Structure of benzyllithium triethylenediamineJournal of the American Chemical Society, 1970
- Progress in the synthesis of polycyclic natural products: The total synthesis of lycopodinePublished by Walter de Gruyter GmbH ,1968