2-(2-Nitroethyl)-1,3-dioxolane as reagent for 3-oxopropyl anion synthon : a new route to jasmonoid and prostaglandin intermediates
- 1 January 1984
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 40 (19), 3809-3814
- https://doi.org/10.1016/s0040-4020(01)88811-6
Abstract
No abstract availableThis publication has 25 references indexed in Scilit:
- A new route to 1,4 -diketones and its application to (z)-jasmone and dihydrojasmone synthesisTetrahedron, 1983
- A New Synthesis of 2-(6-Methoxycarbonylhexyl)-cyclopent-2-en-1-one, An Important Prostanoid SynthonSynthesis, 1983
- Jasmonoid Synthesis from sci-4-Heptenoic AcidBulletin of the Chemical Society of Japan, 1981
- Convenient synthesis of jasmonoid compounds from .gamma.-(trimethylsiloxy)butyronitrileThe Journal of Organic Chemistry, 1980
- Selective alkylation of ethyl 3-oxoglutarate. II. Synthesis of a prostaglandin intermediate and synthesis of dihydrojasmone and methyl dihydrojasmonate.Agricultural and Biological Chemistry, 1979
- Synthesis of Three Jasmin Constituents via a Central IntermediateHelvetica Chimica Acta, 1978
- New route to .gamma.-ketoaldehydes. Application to the synthesis of cis-jasmoneJournal of the American Chemical Society, 1973
- Photochemical decomposition of triphenyltriazafulvenesThe Journal of Organic Chemistry, 1973
- Cyclopentenones. Efficient synthesis of cis-jasomeThe Journal of Organic Chemistry, 1972
- New synthesis of cyclopentenones. Methyl jasmonate and jasmoneThe Journal of Organic Chemistry, 1971