Ruthenium Tetraoxide Oxidation of Alkenes.Part 7. A More Complete Picture.-The main oxidation products of a number of linear and cyclic alkenes are 1,2-diols and/or α-ketols sometimes accompanied by small amounts of scission products such as aldehydes and/or ketones which can be further oxidized to carboxylic acids or can react with the diols to form cyclic acetals, e.g. (XVIII). All reactions proceed through a common intermediate ruthenium(VI) diester, which is presumably the first-formed product from a (3 + 2) cycloaddition of RuO4 to the olefin. -(ALBARELLA, L.; PICCIALLI, V.; SMALDONE, D.; SICA, D.; J.
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.
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.