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The Diels-Alder reaction between substituted 6,6-dimethyl-2-vinylnorpinenes and maleic anhydride
Authors:I. A. Nuretdinov  I. P. Karaseva  V. P. Gubskaya  A. V. Il'yasov
Affiliation:(1) A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan' Scientific Center of the Russian Academy of Sciences, 8 ul. Akad. Arbuzova, 420083 Kazan', Russian Federation
Abstract:Cycloaddition of substituted 6,6-dimethyl-2-vinylnorpinenes with maleic anhydride occursvia the attack of a dienophile on diene from the less hindered side of the bicyclic fragment. IR, UV, CD, and1H NMR spectra of adducts have been studied.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 8, pp. 1546–1548, August, 1995.The authors are grateful to I. E. Ismaev for recording several1H NMR spectra.
Keywords:substituted 6,6-dimethyl-2-vinylnorpinenes  maleic anhydride  Diels-Alder reaction  IR  UV  CD  NMR spectra
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