Acyclic diastereocontrol and asymmetric transmission via anionic oxy-Cope rearrangement. Synthesis of key precursors of (+)-faranal and (−)-antirhine
- 1 January 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (5) , 1025-1042
- https://doi.org/10.1016/s0040-4020(01)86283-9
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- Enantioselective total synthesis of (-)-9-epi-Ambrox, a potent ambergris-type olfactory agentThe Journal of Organic Chemistry, 1991
- Stereocontrolled Construction of Complex Cyclic Ketones via Oxy‐Cope RearrangementAngewandte Chemie International Edition in English, 1990
- Carbonyl Group Regeneration with Substantive Enhancement of Structural ComplexitySynlett, 1990
- The Hetero-Cope Rearrangement in Organic SynthesisSynthesis, 1989
- The thermal, aliphatic Claisen rearrangementChemical Reviews, 1988
- Stereochemically controlled synthesis of steroid side chains: synthesis of desmosterolThe Journal of Organic Chemistry, 1980
- Total synthesis of (.+-.)-coronafacic acid: use of anionic oxy-Cope rearrangements on aromatic substrates in synthesisJournal of the American Chemical Society, 1980
- Stereochemical study of the [3,3] sigmatropic rearrangement of 1,5-diene-3-alkoxides. Application to the stereoselective synthesis of (.+-.)-juvabioneJournal of the American Chemical Society, 1980
- (.+-.)-Periplanone-B. Total synthesis and structure of the sex excitant pheromone of the American cockroachJournal of the American Chemical Society, 1979
- [3,3]Sigmatropic rearrangements of 1,5-diene alkoxides. Powerful accelerating effects of the alkoxide substituentJournal of the American Chemical Society, 1975