The reaction of trialkylboranes with 1,4-naphthoquinone: a new, convenient synthesis of 2-aalkyl-1,4-naphthalenediols. Evidence for a free-radical chain mechanism
- 1 December 1971
- journal article
- research article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 33 (2) , C25-C28
- https://doi.org/10.1016/s0022-328x(00)88388-6
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Iodine as an exceptionally favorable inhibitor for the reaction of oxygen with trialkylboranes. Evidence for a very slow initiation step in the autoxidation of organoboranesJournal of the American Chemical Society, 1971
- Oxygen-induced reactions of organoboranes with acetylacetylene. Convenient new synthesis of .alpha.,.beta.-unsaturated ketones via hydroborationJournal of the American Chemical Society, 1970
- Inhibition of the reaction of organoboranes with .alpha.,.beta.-unsaturated carbonyl derivatives by galvinoxyl. Evidence for a free-radical chain mechanismJournal of the American Chemical Society, 1970
- Oxygen-induced reactions of organoboranes with the inert .alpha.,.beta.-unsaturated carbonyl derivatives. Convenient new aldehyde and ketone synthesis via hydroborationJournal of the American Chemical Society, 1970
- The Preparation of Alkylhydroquinones by the Reductive Alkylation of Quinones with TrialkylboranesJournal of the American Chemical Society, 1965
- The Reductive Alkylation of Quinones with TrialkylboranesJournal of the American Chemical Society, 1964