Application of microwave heating technique for rapid synthesis of γ,δ-unsaturated esters
- 1 February 1995
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 51 (6) , 1809-1816
- https://doi.org/10.1016/0040-4020(94)01058-8
Abstract
No abstract availableKeywords
This publication has 38 references indexed in Scilit:
- Acceleration of the orthoester Claisen rearrangement by clay catalyzed microwave thermolysis: expeditious route to bicyclic lactonesThe Journal of Organic Chemistry, 1992
- Terpenoids to terpenoids: enantioselective construction of 5,6-, 5,7-, and 5,8-fused bicyclic systems. Application to the total synthesis of isodaucane sesquiterpenes and dolastane diterpenesJournal of the American Chemical Society, 1991
- Synthesis of Insecticidally Active 3-Phenoxy Benzyl and α (RS) Cyano-3-Phenoxy Benzyl (±)Trans2-(2, 2-Dichlorovinyl) Spiro (2,5)-Octane-1-CarboxylatesSynthetic Communications, 1988
- An Efficient Synthesis of 4,4-Dimethyl 5-Methylene-γ-ButyrolactoneSynthetic Communications, 1988
- A Base-Mediated Alternative to the Orthoester Claisen RearrangementSynthetic Communications, 1986
- Enantioselective preparation of 3-substituted 4-pentenoic acids via the Claisen rearrangementThe Journal of Organic Chemistry, 1985
- Synthese von 4‐Penten‐4‐oliden (γ‐Methylen‐γ‐butyrolactonen) über 4‐PentensäurenEuropean Journal of Organic Chemistry, 1984
- A New Synthesis of 3,4-Bis[methylene]-hexanedioic Esters from 2-Butynediol via Claisen Orthoester RearrangementSynthesis, 1982
- On the Claisen Rearrangement of Allyl Ethyl Ketene Acetals Generated in situ via Benzeneselenenic Acid EliminiationHelvetica Chimica Acta, 1979
- Reaction of copper enolates of esters with propargylic systems. Facile preparation of 3,4-dienoic esters, stereoselective rearrangement to (2E,4Z)- and (2E,4E)-dienoic esters, and stereoselective synthesis of a fragrance from the Bartlett pearThe Journal of Organic Chemistry, 1978