Formation of Substituted Cyclobutanes in the Reaction of 2-(2-Methyl-2-propenyl)-3-chloromethyloxirane with Aromatic Hydrocarbons.-The title reaction in the presence of AlCl3 gives substituted cyclobutanes (III) (5 examples) in good yields. Further cyclobutane derivatives (IV), (V) or (VII) are available by simple side chain modifications of (III). -(AKHMEDOV, M. A.; SARDAROV, I. K.; AKHMEDOV, I. M.; KOSTIKOV, R. R.; KISIN, A. V.; BABAEV, N. M.; Zh.
ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
1992 cleavage reactions, decomposition reactions, pyrolysis cleavage reactions, decomposition reactions, pyrolysis O 0100 30 -067 Reaction of 2-(2-Propenyl)-3-chloromethyloxirane with Benzene. -The title reaction leads to the products (III)-(V). In addition, oxidation of these compounds is carried out. -(AKHMEDOV, M. A.; SARDAROV, I. K.; AKHMEDOV, I. M.; KOSTIKOV, R. R.; BABAEV, N. M.; SHUKYUROVA, M. B.; Zh. Org. Khim. 27 (1991) 11, 2285-2289; Inst. khlororg. sint. Akad. nauk Azerbaijan, Sumgait, Azerbaijan; RU)
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.