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1
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For reviews on sydnones, see: (a) Stewart, F. H. C. Chem. Rev. 1964, 64, 129.
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Stewart, F.H.C.1
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5
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(b) Hill, J. B.; Ray, R. E.; Wagner, H.; Aspinall, R. L. J. Med. Chem. 1975, 18, 50.
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Aspinall, R.L.4
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7
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(d) Moustafa, M. A.; Gineinah, M. M.; Nasr, M. N.; Bayoumi, W. A. H. Arch. Pharm. (Weinheim) 2004, 337, 164.
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Nasr, M.N.3
Bayoumi, W.A.H.4
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8
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(a) Geoffroy, I.; Carre, B.; Lemordant, D.; Herreyre, S.; Biensan, Ph. ITE Lett. Batter., New Technol. Med. 2000, 1, 20.
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(b) Chan, W.; Zhang, W.; Szeto, Y. Mater. Lett. 2000, 42, 280.
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(c) Tien, H.; Hwang, Y.; Wen, T. J. Chin. Chem. Soc. 1998, 45, 209.
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11
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63849341095
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Sasaki, Y.; Hirobomi, O.; Handa, M. Nippon Kagaku Kaishi 1993, 11, 1217; Chem. Abstr. 1994, 120, 34459t.
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Sasaki, Y.; Hirobomi, O.; Handa, M. Nippon Kagaku Kaishi 1993, 11, 1217; Chem. Abstr. 1994, 120, 34459t.
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13
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(b) Vasil'eva, V. F.; Yashunskii, V. G.; Shchukina, M. N. Zh. Obshch. Khim. 1960, 30, 698.
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Shchukina, M.N.3
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14
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36549038697
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For a recent example of this reactivity, see
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For a recent example of this reactivity, see: Browne, D. L.; Helm, M. D.; Plant, A.; Harrity, J. P. A. Angew. Chem. Int. Ed. 2007, 46, 8656.
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Plant, A.3
Harrity, J.P.A.4
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15
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0034112044
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For the transformation of sydnones into oxadiazolinones with bromine in acetic anhydride, see
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For the transformation of sydnones into oxadiazolinones with bromine in acetic anhydride, see: Mallur, S. G.; Badami, B. V. Farmaco 2000, 55, 65.
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(a) Greco, C. V.; Pesce, M.; Franco, J. M. J. Heterocycl. Chem. 1966, 3, 391.
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19
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0001568295
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For representative examples, see: a
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For representative examples, see: (a) Pivsa-Art, S.; Satoh, T.; Kawamura, Y.; Miura, M.; Nomura, M. Bull. Chem. Soc. Jpn. 1998, 71, 467.
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Nomura, M.5
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(b) Bellina, F.; Calandri, C.; Cauteruccio, S.; Rossi, R. Tetrahedron 2007, 63, 1970.
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Tetrahedron
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Bellina, F.1
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(c) Flegeau, E. F.; Popkin, M. E.; Greaney, M. F. Org. Lett. 2008, 10, 2717.
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(d) For reviews, see: Martin, T.; Verrier, C.; Hoarau, C.; Marsais, F. Org. Lett. 2008, 10, 2909.
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(g) Alberico, D.; Scott, M. E.; Lautens, M. Chem. Rev. 2007, 107, 174.
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Alberico, D.1
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27
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44149100021
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This mechanism was reported for the Pd-catalysed direct cross-coupling reactions of adenosines with aryl iodides: Storr, T. E, Firth, A. G, Wilson, K, Darley, K, Baumann, C. G, Fairlamb, I. J. S. Tetrahedron 2008, 64, 6125
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This mechanism was reported for the Pd-catalysed direct cross-coupling reactions of adenosines with aryl iodides: Storr, T. E.; Firth, A. G.; Wilson, K.; Darley, K.; Baumann, C. G.; Fairlamb, I. J. S. Tetrahedron 2008, 64, 6125.
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28
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84943701775
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These results suggest that this is a 'Type 1' cycloaddition: Sustmann, R
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These results suggest that this is a 'Type 1' cycloaddition: Sustmann, R. Pure Appl. Chem. 1974, 40, 569.
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Pure Appl. Chem
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