Pregled bibliografske jedinice broj: 82191
Diels-Alder Cycloadditions of 1, 3-Cyclohexadien-4, 5-diones (o-benzoquinones). Part I. Synthesis
Diels-Alder Cycloadditions of 1, 3-Cyclohexadien-4, 5-diones (o-benzoquinones). Part I. Synthesis, 2000. (ostalo).
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Naslov
Diels-Alder Cycloadditions of 1, 3-Cyclohexadien-4, 5-diones (o-benzoquinones). Part I. Synthesis
Autori
Johnston, Martin R. ; Latter, Melissa J. ; Warrener, Ronald N. ; Golić, Mirta ; McKavanagh, D. ; Margetić, Davor
Izvornik
Fourth International Electronic Conference on Synthetic Organic Chemistry (ECSOC-4), Paper No: A0057, http://www.unibas.ch/mdpi/ecsoc-4.htm, September 1-30. 2000, Editors: Thomas Wirth, C. Oliver Kappe, Eduard Felder, Ulf Diederichsen and Shu- Kun Lin, CD-
Vrsta, podvrsta
Ostale vrste radova, ostalo
Godina
2000
Ključne riječi
cycloadditions; Diels-Alder; norbornenes
Sažetak
Cycloadditions between o-chloranil and norbornadiene produced a range of geometrical variants which were characterised as quinoxaline derivatives. Two ether by-products were also observed resulting from hetero Diels-Alder reaction. Photochemical irradiation of 20 produced the cage compound 22 as a result of (2+2)pi cycloaddition.
Izvorni jezik
Engleski
