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1. Part IX in the Series "The Chemistry of Coumarin Derivatives". Part VIII: Appendino, G.; Cravotto, G.; Palmisano, G.; Annunziata, R. Synth. Commun. 1996, 26, 3359.
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The toxins of Ferula communis L
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8. P. hospiton is one of the only four insects included in the appendix 1 of CITES (Convention on International Trade in Endangered Species) (IUCN Red Data Book). For a monography, see: Kettlewell, H.B.D. Entomologist 1955, 88, 280.
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b) For a recent review, see: Li, C.-J. Tetrahedron 1996, 52, 5643.
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For leading references, see: (a) ref. 9b
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12. For leading references, see: (a) ref. 9b.
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(b) Li, C.-J. Chem Rev. 1993, 93, 2023.
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14. Adam, W.; Mitchell, C.M.; Paredes, R.; Smerz, A.K.; Veloza, L.A. Liebigs Ann/Recueil 1997, 1365. See also: Appendino, G.; Tagliapietra, S.; Gariboldi, P.; Nano, G.M.; Picci, V. Phytochemistry 1988, 27, 3619.
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0001193618
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14. Adam, W.; Mitchell, C.M.; Paredes, R.; Smerz, A.K.; Veloza, L.A. Liebigs Ann/Recueil 1997, 1365. See also: Appendino, G.; Tagliapietra, S.; Gariboldi, P.; Nano, G.M.; Picci, V. Phytochemistry 1988, 27, 3619.
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Picci, V.5
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26
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85038531846
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note
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15. (table presented)
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27
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85038528354
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note
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16. The reactions involved in the putative biogenetic relationship between ferulenol and fercoprolone (double bond photooxygenation/epoxidation and hydroperoxide fragmentation/epoxide opening, Scheme 1) can also be invoked to rationalise the occurrence of other oxidised derivatives of ferulenol, suggesting that a general strategy of oxidative modification underlies the bewildering chemical diversity of the coumarinyl meroterpenoids from F. communis.
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