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(b) Eurycoma longifolia Jack: Kuo, P.-C.; Shi, L.-S.; Damu, A. G.; Su, C.-R.; Huang, C.-H.; Ke, C.-H.; Wu, J.-B.; Lin, A.-J.; Bastow, K. F.; Lee, K.-H.; Wu, T.-S. J. Nat. Prod. 2003, 66, 1324-1327, and references therein.
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7
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For a recent example from Caryophyllaceae (Drymaria diandra Bl.): Hsieh, P.-W.; Chang, F.-R.; Lee, K.-H.; Hwang, T.-L.; Chang, S.-M.; Wu, Y.-C. J. Nat. Prod. 2004, 67, 1175-1177.
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Fleischhuaer7
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10
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12
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29044443744
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14
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29044447180
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note
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Also previously isolated from other Zanthoxylum species, see ref 3b.
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-
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15
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29044444301
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note
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A full account of this new reaction will be disclosed in due course.
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-
16
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15944376218
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(a) For recent examples of access to the general canthine skeleton, see: Lindsley, C. W.; Bogusky, M. J.; Leister, W. H.; McLain, R. T.; Robinson, R. G.; Barnett, S. F.; Defeo-Jones, D.; Ross, C. W., III; Hartman, G. D. Tetrahedron Lett. 2005, 46, 2779-2782.
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Barnett, S.F.6
Defeo-Jones, D.7
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20
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12344315990
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(b) For recent access to the canthin-6-one skeleton, see inter alia: Suzuki, H.; Adachi, M.; Ebihara, Y.; Gyoutoku, H.; Furuya, H.; Murakami, Y.; Okuno, H. Synthesis 2005, 28-32.
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3 in Bischler-Napieralski cyclizations in different reaction conditions, see, inter alia: (a) Snyder, H. R.; Werber, F. X. J. Am. Chem. Soc. 1950, 72, 2962-2965.
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1242285000
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For a similar case, where benzene (caution) was chosen as the solvent for a Bischler-Napieralski cyclization, see: Santos, L. S.; Pilli, R. A.; Rawal, V. H. J. Org. Chem. 2004, 69, 1283-1289.
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Santos, L.S.1
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41
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23944508734
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In the course of the revision of the manuscript, another access to benzocanthinones was published, see: Markgraf, J. H.; Dowst, A. A.; Hensley, L. A.; Jakobsche, C. E.; Kaltner, C. J.; Webb, P. J.; Zimmerman, P. W. Tetrahedron 2005, 61, 9102-9110.
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Markgraf, J.H.1
Dowst, A.A.2
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Jakobsche, C.E.4
Kaltner, C.J.5
Webb, P.J.6
Zimmerman, P.W.7
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42
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29044437096
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note
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Kindly provided by F. Dromer, CNRMA, Institut Pasteur, Paris, France.
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