Effective, thermal one-carbon + two-carbon cycloaddition of cyclopropenone ketals with electron-deficient olefins: Cyclopropane formation.
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (49) , 5611-5614
- https://doi.org/10.1016/s0040-4039(01)91393-0
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- An effective, thermal three-carbon + two-carbon cycloaddition for cyclopentenone formation: formal 1,3-dipolar cycloaddition of cyclopropenone ketalsJournal of the American Chemical Society, 1984
- Nickel-catalyzed reactions involving strained bonds. 17. Nickel(0)-catalyzed reactions of bicyclo[1.1.0]butanes. Geminal two-bond cleavage reaction and the stereospecific olefin trapping of the carbenoid intermediateThe Journal of Organic Chemistry, 1981
- Dual reactivity of 3,3-dimethoxycyclopropeneThe Journal of Organic Chemistry, 1977
- Reaction of cyclopropenone ketals with alcoholsThe Journal of Organic Chemistry, 1977
- CYCLOPROPENONEOrganic Syntheses, 1977
- Synthesis and some reactions of 3,3-dimethoxycylopropeneThe Journal of Organic Chemistry, 1972