A general synthetic approach to 5-alkyl-2(5H)furanonesvia 1,3-dipolar cycloaddition
- 1 May 1998
- journal article
- Published by Elsevier BV in Tetrahedron
- Vol. 54 (21), 5695-5708
- https://doi.org/10.1016/s0040-4020(98)00258-0
Abstract
No abstract availableThis publication has 28 references indexed in Scilit:
- Palladium-Catalyzed Cyclocarbonylation of Terminal and Internal Alkynols to 2(5H)-FuranonesThe Journal of Organic Chemistry, 1997
- Ring-opening of substituted isoxazolidines: one-pot synthesis of indenesTetrahedron, 1993
- Ring-opening of Isoxazolidine Nucleus by Trimethyl Posphate Treatment: Formation of Tertiary Allylic Alcohols via Intermediate 1,3-Oxazinium SaltsHETEROCYCLES, 1993
- A New Synthesis of Streptomyces Lactones by 1,3-Dipolar CycloadditionHETEROCYCLES, 1993
- Synthesis of ethisolide, isoavenaciolide, and avenaciolideThe Journal of Organic Chemistry, 1992
- A New Method for the Synthesis of 3,5-Disubstituted 2(5H)-Furanones. Synthesis of (±)-Acarenoic AcidBulletin of the Chemical Society of Japan, 1987
- A Short-step Synthesis of 4-HydroxyprolineBulletin of the Chemical Society of Japan, 1981
- Synthese von α‐Alkyl‐ und α,α′‐Dialkylmuconsäuren auf dem Wege der (2 + 2)‐Cycloaddition von Acetylen an Alkylderivate des MaleinsäureanhydridsEuropean Journal of Organic Chemistry, 1977
- Fungicidal constituents in "kuntan" (calcined rice chaff) smoke.Agricultural and Biological Chemistry, 1977
- Studies on mushroom flavoursZeitschrift für Lebensmittel-Untersuchung und Forschung, 1976