The preparation of synthons on route to terpenoids of marine origin
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (36) , 3417-3420
- https://doi.org/10.1016/s0040-4039(01)95424-3
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Isolation and structure of angasiolThe Journal of Organic Chemistry, 1978
- Obtusadiol, a unique bromoditerpenoid from the marine red alga Laurencia ObtusaTetrahedron Letters, 1978
- Interesting aspects of marine natural products chemistryTetrahedron, 1977
- Antineoplastic agents. 48. The isolation and structure of aplysistatinJournal of the American Chemical Society, 1977
- Bromonium ion-induced cyclization of methyl farnesate: application to the synthesis of snyderol.Tetrahedron Letters, 1976
- Stereoselectivity of the rearrangement of allyl siloxyvinyl ethers. Highly stereoselective synthesis of a diol found in the pheromonal secretion of the queen butterflyThe Journal of Organic Chemistry, 1974
- Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squaleneJournal of the American Chemical Society, 1970
- Notes- Reactions of Ethyl Isobutenyl EtherThe Journal of Organic Chemistry, 1960
- Homogeneous Metal Salt Catalysis in Organic Reactions. I. The Preparation of Vinyl Ethers by Vinyl TransetherificationJournal of the American Chemical Society, 1957
- Über die Umlagerung einiger Äthersäurechloride in Chlorsäure‐esterBerichte der deutschen chemischen Gesellschaft (A and B Series), 1941