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1
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0039227605
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note
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Contribution Number 522 from the Photochemistry Unit, The University of Western Ontario. Financial support from the Natural Sciences and Engineering Research Council of Canada (NSERC) is gratefully acknowledged.
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2
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0002561392
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Horspool, W.M. (ed.), Plenum, New York
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Weedon, A.C. in Synthetic Organic Photochemistry, Horspool, W.M. (ed.), Plenum, New York, 1984, pp 61-144.
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Cantrell, T.S. Tetrahedron 1971, 27, 1227; Agosta, W.C.; Lowrance, W.W. J. Org. Chem. 1970, 35, 3851.
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Cantrell, T.S. Tetrahedron 1971, 27, 1227; Agosta, W.C.; Lowrance, W.W. J. Org. Chem. 1970, 35, 3851.
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For the preparation of 3-nitro-2-cyclohexenone see: Garbisch, E.W. J. Org. Chem. 1965, 30, 2109; Vankar, Y.D.; Bawa, A. Synthetic Commun. 1985, 15, 1253.
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For the preparation of 3-nitro-2-cyclohexenone see: Garbisch, E.W. J. Org. Chem. 1965, 30, 2109; Vankar, Y.D.; Bawa, A. Synthetic Commun. 1985, 15, 1253.
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For a recent review of the photochemical reactivity of the nitro group see Döpp D. in CRC Handbook of Organic Photochemistry and Photobiology, Horspool, W.M.; Song, P.-S. (eds), CRC Press, Boca Raton, 1994, Chapter 81, pp 1019-1062.
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Döpp, D.1
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0039819464
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Irradiations were conducted using Pyrex and water filtered light from a medium pressure mercury lamp.
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0041006127
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In the photocycloaddition reaction between 2-cyclohexenone and 2-methylpropene compound 4, R=H, is formed as a mixture of cis and trans fused adducts; the trans fused isomer was epimerized to the more stable cis fused isomer 8 when the mixture was hydrogenated.
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