Chemistry of Heterocyclic Compounds p. 721 - 724 (1988)
Update date:2022-08-03
Topics: IR spectroscopy Regioselectivity NMR spectroscopy Stereochemistry Thermolysis Chromatography Mass spectrometry (MS) Ketone X-ray crystallography Reaction Mechanism Cycloaddition Ring-Opening Reaction Activation Energy Thermal Transformations Kinetic Control Thermodynamic Control Rearrangement Reaction Benzylidene Diradical intermediate Spirocyclic Compound
Anokhina, I. K.
Fedorova, N. G.
Zalukaev, L. P.
Krysin, M. Yu.
2-Phenyl-3,3,4,4-diphthaloyloxetane is formed when solutions of 2-benzylideneindan-1,3-dione α-oxide in benzene or carbon tetrachloride are heated, while 5-oxo-3-phenyl-2,2-phthaloyl-2,3-dihydroindeno<2,3-b><1,4>dioxine is formed when solutions in dioxane are heated.
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Doi:10.1246/cl.1984.1359
(1984)Doi:10.1021/jo8005649
(2008)Doi:10.1002/adsc.201801670
(2019)Doi:10.1021/ja01156a562
(1951)Doi:10.1021/ol070412d
(2007)Doi:10.1016/S0040-4020(01)90292-3
(1987)
