Intramolecular 1,3-diyl trapping reactions: Total synthesis of the marine natural product (, )Δ9(12)-capnellene
- 1 January 1981
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 22 (44) , 4389-4392
- https://doi.org/10.1016/s0040-4039(01)82964-6
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Intramolecular diyl trapping. Total synthesis of dl-hirsuteneJournal of the American Chemical Society, 1981
- Synthesis applications of directed 2-azonia-[3,3]-sigmatropic rearrangements. 4. A new method for stereoselective piperidine annulation. Directing the 2-azonia-[3,3]-sigmatropic rearrangement by irreversible hydrolysisThe Journal of Organic Chemistry, 1980
- Effect of A(1,3) strain on the stereochemical course of N-acyliminium ion cyclizationsJournal of the American Chemical Society, 1980
- Electrochemical generation of the azo linkage. Synthesis of bicyclic azo compounds, precursors of 1,3-diylsThe Journal of Organic Chemistry, 1979
- A regiospecific and highly stereoselective approach to the synthesis of linearly fused tricyclopentanoids. Intramolecular diyl trapping reactionsJournal of the American Chemical Society, 1979
- Chemical Studies of Marine Invertebrates. XL. Δ9 (12)‐Capnellene‐2β, 5α, 8β, 10α‐Tetrol, a New Sesquiterpene Alcohol from the Soft Coral Capnella ImbricataBulletin des Sociétés Chimiques Belges, 1979
- A new, mild method for the synthesis of azo compoundsThe Journal of Organic Chemistry, 1978
- Measurements of Bijvoet differences. Structure and absolute configuration of africanol, a sesquiterpeneActa Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 1976
- Allylic strain in six-membered ringsChemical Reviews, 1968
- Über eine neue Fulven-SyntheseAngewandte Chemie, 1963