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Surprisingly efficient intramolecular addition of carbon radicals to carbonyl groups: a ready route to cycloalkanols

Ray Tsang, +1 more
- 01 Dec 1986 - 
- Vol. 108, Iss: 25, pp 8102-8104
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This article is published in Journal of the American Chemical Society.The article was published on 1986-12-01. It has received 53 citations till now. The article focuses on the topics: Acetal & Free-radical reaction.

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Distonic radical cations in gaseous and condensed phase

TL;DR: In this paper, the authors demontre que les radicaux cationiques CH 3 OH +, CH 3 NH 2 + and CH 3 ClH + ont des isomeres stables.
Journal ArticleDOI

Radical-Mediated 1,2-Formyl/Carbonyl Functionalization of Alkenes and Application to the Construction of Medium-Sized Rings

TL;DR: A novel radical 1, 2-formylfunctionalization of alkenes involving 1,2(4,5)-formyl migration triggered by addition of various carbon- and heteroatom-centered radicals has been developed for the first time, thus providing straightforward access to diverse β-functionalized aldehydes with good efficiency, remarkable selectivity, and excellent functional group tolerance.
Journal ArticleDOI

Radicals from Epoxides. Intramolecular Addition to Aldehyde and Ketone Carbonyls

TL;DR: The behavior of epoxy alcohols with titanocene chloride to afford saturated diols and epoxy esters that give unsaturated hydroxy esters are discussed in this paper.
Journal ArticleDOI

Developments in cyclisation reactions

TL;DR: Cyclisations cationiques, radicalaires and anioniques as discussed by the authors are catalysees par des metaux, and they can be classified into three classes: cationique, radicalaine and radicalaine.
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