Total synthesis of (.+-.)-dihydropinidine, (.+-.)-monomorine I, and (.+-.)-indolizidine 223AB (gephyrotoxin 223AB) by intramolecular nitroso Diels-Alder reaction
- 31 July 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 54 (17) , 4088-4097
- https://doi.org/10.1021/jo00278a020
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Asymmetric synthesis. 2. Practical method for the asymmetric synthesis of indolizidine alkaloids: total synthesis of (-)-monomorine IThe Journal of Organic Chemistry, 1985
- A formal total synthesis of ipalbidineJournal of the Chemical Society, Perkin Transactions 1, 1985
- Stereoselective indolizidine synthesis: preparation of stereoisomers of gephyrotoxin-223ABThe Journal of Organic Chemistry, 1982
- Alkaloid synthesis via intramolecular ene reaction. 2. Application to dl-mesembrine and dl-dihydromaritidineThe Journal of Organic Chemistry, 1982
- The structure of gephyrotoxin (GTX) 223ABCellular and Molecular Life Sciences, 1981
- Stereochemistry of the Robinson-Schoepf reaction. A stereospecific total synthesis of the ladybug defense alkaloids precoccinelline and coccinellineJournal of the American Chemical Society, 1979
- 13C nmr assignments of selected octahydroindolizinesJournal of Heterocyclic Chemistry, 1979
- Classification of skin alkaloids from neotropical poison-dart frogs (dendrobatidae)Toxicon, 1978
- The stereochemistry of pinidineTetrahedron, 1965
- Pinus Alkaloids. The Alkaloids of P. sabiniana Dougl. and Related SpeciesJournal of the American Chemical Society, 1955