PHOTOREARRANGEMENT OF 2,3-DIMETHYL-4,5-DIHYDROFURAN AND 2-METHYL-4,5-DIHYDROFURAN
- 1 May 1965
- journal article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 43 (5) , 1417-1418
- https://doi.org/10.1139/v65-191
Abstract
Irradiation of an ether solution of the title compounds with a medium-pressure mercury are gave in each case a rearrangement reaction, with formation of an acetyl cyclopropane isomer as the major product. This reaction is similar to that induced thermally at 450°.Keywords
This publication has 6 references indexed in Scilit:
- Phenylated Dihydrofurans. Photo- and Acid-Catalyzed Rearrangements and Intermediacy in Cyclopropyl Ketone CleavageJournal of the American Chemical Society, 1964
- The Photolysis of Ethyl Vinyl EtherJournal of the American Chemical Society, 1961
- III. Mechanism of the Formation of Limonene SulfidesJournal of the American Chemical Society, 1959
- A New Technique in Preparing 2,4-Dinitrophenylhydrazones. Use of Diglyme as SolventThe Journal of Organic Chemistry, 1959
- MECHANISM OF HYDROGENATION OF 2-METHYLFURANThe Journal of Organic Chemistry, 1951
- Reactions of Furan Compounds. VII. Thermal Interconversion of 2,3-Dihydrofuran and Cyclopropane Aldehyde1Journal of the American Chemical Society, 1947