Medium ring synthesis via intramolecular diels-alder reaction. I. The synthesis of bicyclo[6.4.O]dodecane systems
- 1 January 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (20) , 2081-2084
- https://doi.org/10.1016/s0040-4039(01)81166-7
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Synthetic studies on the taxane diterpenes. Utility of the intramolecular Diels-Alder reaction for a single-step, stereocontrolled synthesis of a taxane model systemJournal of the American Chemical Society, 1983
- Rapid and efficient construction of the ophiobolin nucleusThe Journal of Organic Chemistry, 1983
- Ozonolytic cleavage of cycloalkenes to terminally differentiated productsTetrahedron Letters, 1982
- A [4 + 4] annulation approach to eight-membered carbocyclic compoundsJournal of the American Chemical Society, 1982
- Diels-Alder reactions of cycloalkenones. 1. Preparation and structure of the adductsThe Journal of Organic Chemistry, 1982
- Preparation and rearrangement of 1,2-dialkenylcyclobutanols. A useful method for synthesis of substituted cyclooctenonesThe Journal of Organic Chemistry, 1982
- Stereochemical aspects of the intramolecular Diels-Alder reactions of deca-2,7,9-trienoate esters. 3. Thermal, Lewis acid catalyzed, and asymmetric cyclizationsJournal of the American Chemical Society, 1982
- Ring closure reactions of bifunctional chain moleculesAccounts of Chemical Research, 1981
- Intramolecular [4+2] and [3+2] Cycloadditions in Organic SynthesisAngewandte Chemie International Edition in English, 1977
- Frontier molecular orbital theory of cycloaddition reactionsAccounts of Chemical Research, 1975