Tetrahedron Letters p. 5707 - 5708 (1985)
Update date:2022-08-16
Topics: Yield Catalyst Decomposition Solvent Thermolysis Synthetic route Rearrangement Chromatography Cyclization Mechanism Intermediate Activation Energy Spectroscopic Analysis Ylide Heterocyclic compound Reactive species Carbonyl Group (C=O)
Darwen, Stuart P.
Smalley, Robert K.
3H-Indazol-3-one has been generated by thermolysis of N(o-azidobenzoyl)iminopyridinium ylide, and trapped as its Diels-Alder cycloadducts with several dienes.
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Doi:10.1021/jo00374a001
(1986)Doi:10.1016/j.tetlet.2017.11.005
(2017)Doi:10.1002/cjoc.201900134
(2019)Doi:10.1080/00397911.2021.1939060
(2021)Doi:10.1002/ps.2780420407
(1994)Doi:10.1016/S0040-4020(01)89841-0
(1988)
