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1
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0029971797
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Some representative examples, include: (a) Wall, M. E.; Wani, M. C. J. Ethnopharmacol. 1996, 51, 239-253.
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Some representative examples, include: (a) Wall, M. E.; Wani, M. C. J. Ethnopharmacol. 1996, 51, 239-253.
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-
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2
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33746279633
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Lupin alkaloids: (b) Gray, D.; Gallagher, T. Angew. Chem., Int. Ed. 2006, 45, 2419-2423.
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Lupin alkaloids: (b) Gray, D.; Gallagher, T. Angew. Chem., Int. Ed. 2006, 45, 2419-2423.
-
-
-
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3
-
-
0011911259
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-
Cerpegin: c
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Cerpegin: (c) Adibatti, N. A.; Thirugnanasambantham, P.; Kulothungan, C.; Viswanathan, S.; Kameswaran, L.; Balakrishna, K.; Sukumar, E. Phytochemistry 1991, 30, 2449-2450.
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Adibatti, N.A.1
Thirugnanasambantham, P.2
Kulothungan, C.3
Viswanathan, S.4
Kameswaran, L.5
Balakrishna, K.6
Sukumar, E.7
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4
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0016018735
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Mappicine: d
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Mappicine: (d) Govindachari, T. R.; Ravindranath, K. R.; Viswanathan, N. J. Chem. Soc., Perkin Trans. 1 1974, 1215-1217.
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Govindachari, T.R.1
Ravindranath, K.R.2
Viswanathan, N.3
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5
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0034811275
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Some representative examples, include: (a) Huffman, J. W.; Lu, J.; Hynd, G.; Wiley, J. L.; Martin, B. R. Bioorg. Med. Chem. 2001, 9, 2863-2870.
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Some representative examples, include: (a) Huffman, J. W.; Lu, J.; Hynd, G.; Wiley, J. L.; Martin, B. R. Bioorg. Med. Chem. 2001, 9, 2863-2870.
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7
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27644550959
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and references therein. Review: a
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Review: (a) Torres, M.; Gil, S.; Parra, M. Curr. Org. Chem. 2005, 9, 1757-1779, and references therein.
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Curr. Org. Chem
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Torres, M.1
Gil, S.2
Parra, M.3
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9
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0028838528
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(b) Liu, H.; Ko, S.-B.; Josien, H.; Curran, D. P. Tetrahedron Lett. 1995, 36, 8917-8920.
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Tetrahedron Lett
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Liu, H.1
Ko, S.-B.2
Josien, H.3
Curran, D.P.4
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10
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Conreaux, D.; Bossharth, E.; Monteiro, N.; Desbordes, P.; Balme, G. Tetrahedron Lett. 2005, 46, 7917-7920.
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Tetrahedron Lett
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Conreaux, D.1
Bossharth, E.2
Monteiro, N.3
Desbordes, P.4
Balme, G.5
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Ruda, M. C.; Bergman, J.; Wu, J. J. Comb. Chem. 2002, 4, 530-535.
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Itami, K.1
Yamazaki, D.2
Yoshida, J.-I.3
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15
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18844460949
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Benzylacetamide is presumed to form via a Ritter process, see: a
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Benzylacetamide is presumed to form via a Ritter process, see: (a) Ritter, J. J.; Minieri, P. P. J. Am. Chem. Soc. 1948, 70, 4045-4048.
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Ritter, J.J.1
Minieri, P.P.2
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16
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0000176481
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Beak, P.; Bonham, J.; Lee, J. T., Jr. J. Am. Chem. Soc. 1968, 90, 1569-1582.
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Beak, P.1
Bonham, J.2
Lee Jr., J.T.3
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17
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0043284167
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The incomplete thermal rearrangement of alkoxypyridines to give the corresponding (N)-alkyl pyridones using flash vacuum pyrolysis at 600°C has been observed previously, see: (a) Lister, T.; Prager, R. H.; Tsaconas, M.; Wilkinson, K. L. Aust. J. Chem. 2003, 56, 913-916.
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The incomplete thermal rearrangement of alkoxypyridines to give the corresponding (N)-alkyl pyridones using flash vacuum pyrolysis at 600°C has been observed previously, see: (a) Lister, T.; Prager, R. H.; Tsaconas, M.; Wilkinson, K. L. Aust. J. Chem. 2003, 56, 913-916.
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