Diels-alder cyclization of 2,8,10-undecatrienals as a route to 1,2,3,4,4a,5,6,8a-octahydronaphthalenes
- 1 January 1986
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 42 (11) , 2893-2902
- https://doi.org/10.1016/s0040-4020(01)90578-2
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- Kijanimicin. Part 3. Structure and absolute stereochemistry of kijanimicinJournal of the Chemical Society, Perkin Transactions 1, 1983
- Synthesis of the bottom half of chlorothricolideThe Journal of Organic Chemistry, 1982
- Intramolecular Diels-Alder reaction of undeca-2,8,10-trienoate.CHEMICAL & PHARMACEUTICAL BULLETIN, 1982
- Intramolecular Diels-Alder reactions: the angularly methylated trans-perhydroindan ring systemJournal of the American Chemical Society, 1981
- Approach to the total synthesis of chlorothricolide: synthesis of "7-epi-bottom half" and its union with "top half" systemsThe Journal of Organic Chemistry, 1981
- Kijanimicin. 1. Structures of the individual sugar componentsJournal of the American Chemical Society, 1981
- Molecular sieve-assisted oxidations: new methods for carbohydrate derivative oxidationsJournal of the Chemical Society, Chemical Communications, 1980
- An approach to the total synthesis of chlorothricolide: the synthesis of the top halfThe Journal of Organic Chemistry, 1979
- Heuristic Programming as an Ion Generator in Mass Spectrometry. I. Generation of Primary Ions with Charge LocalizationHelvetica Chimica Acta, 1972
- Mass spectrometry in structural and stereochemical problems. CCIX. Functional group interaction after electron impact. Anomalous ether cleavage in bifunctional benzyloxy ethersThe Journal of Organic Chemistry, 1971