A formal CH insertion reaction of an aryl nitrene into an alkyl CH bond. Implications for photoaffinity labelling.
- 31 December 1986
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 27 (7) , 791-794
- https://doi.org/10.1016/s0040-4039(00)84102-7
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Chemistry of fluorenylidene at low temperaturesJournal of the American Chemical Society, 1978
- Reactions of carbenes at low temperatures. Diphenylcarbene and isobuteneJournal of the American Chemical Society, 1978
- Reactions of methylphenylcarbene and phenylcarbene in isobutene matrices: origins of the "insertion" productsJournal of the American Chemical Society, 1977
- Competitive cyclisation of singlet and triplet nitrenes. Part III. The effect of temperature on tile reactivity of thermally and photochemically derived arylnitrenesTetrahedron Letters, 1976
- Intermolecular aromatic substitution by aryl nitrenesThe Journal of Organic Chemistry, 1972
- Spin state of photogenerated phenylnitreneJournal of the American Chemical Society, 1971
- Photolysis of phenyldiazomethane in olefinic matrices. Chemistry of triplet phenylcarbeneJournal of the American Chemical Society, 1971
- Intermolecular aromatic substitution by aryl-nitrenesJournal of the Chemical Society D: Chemical Communications, 1970
- Evidence for the involvement of triplet phenyl nitrene in intermolecular C-H insertionJournal of the American Chemical Society, 1968
- Insertion reactions of aryl nitrenesTetrahedron Letters, 1965