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5
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0343962680
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3
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7
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0028072131
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DDQ
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DDQ: J.J. Naleway, C.M.J. Fox, D. Robinbold, E. Terpetschnig, N.A. Olson, and R.P. Haugland Tetrahedron Lett. 35 1994 8569 8572
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Haugland, R.P.6
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10
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84865204040
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There are a few reports of the oxidative synthesis of 5 from benzylic alcohols as aldehyde precursors with anthranilamides in the presence of transition metal catalysts. For examples, see
-
There are a few reports of the oxidative synthesis of 5 from benzylic alcohols as aldehyde precursors with anthranilamides in the presence of transition metal catalysts. For examples, see: H. Hikawa, Y. Ino, H. Suzuki, and Y. Yokoyama J. Org. Chem. 77 2012 7046 7051
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13
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63149132683
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Alternatively, 5 are synthesized via the condensation of anthranilamides and carboxylic acids and their derivatives and subsequent dehydrative cyclization of the resulting amides. For recent examples, see
-
Alternatively, 5 are synthesized via the condensation of anthranilamides and carboxylic acids and their derivatives and subsequent dehydrative cyclization of the resulting amides. For recent examples, see: F. Gellibert, M.H. Fouchet, V.L. Nguyen, R. Wang, G. Krysa, A.C. Gouville, S. Huet, and N. Dodic Bioorg. Med. Chem. Lett. 19 2009 2277 2281
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Gouville, A.C.6
Huet, S.7
Dodic, N.8
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18144364686
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A.V. Purandare, A. Gao, H. Wan, J. Somerville, C. Burke, C. Seachord, W. Vaccaro, J. Wityak, and M.A. Poss Bioorg. Med. Chem. Lett. 15 2005 2669 2672
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Seachord, C.6
Vaccaro, W.7
Wityak, J.8
Poss, M.A.9
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F. Minisci, F. Recupero, A. Cecchetto, C. Punta, and C. Gambarotti J. Heterocycl. Chem. 40 2003 325 328
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77955123779
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For an example of the synthesis of 5s via oxidative cyclization protocol, see
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For an example of the synthesis of 5s via oxidative cyclization protocol, see: G.-W. Wang, C.-B. Miao, and H. Kang Bull. Chem. Soc. Jpn. 79 2006 1426 1430
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Kang, H.3
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24
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84655167959
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For examples of the synthesis 8 via oxidative cyclization, see
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For examples of the synthesis 8 via oxidative cyclization, see: M. Adib, E. Sheikhi, and H.R. Bijanzadeh Synlett 2012 85 88
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79957487229
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M.-J. Hour, J.-S. Yang, T.-L. Chen, K.-T. Chen, S.-C. Kuo, J.-G. Chung, C.-C. Lu, C.-Y. Chen, and Y.-H. Chuang Eur. J. Med. Chem. 46 2011 2709 2721
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Chen, C.-Y.8
Chuang, Y.-H.9
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28
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63849295076
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For recent examples, see
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For recent examples, see: A.I. Mikhaleva, A.V. Ivanoc, E.V. Skitaltseva, I.A. Ushakov, A.M. Vasiltsov, and B.A. Trofimov Synthesis 2009 587 590
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84897990919
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Indian Pat. Appl., IN 2004DE00394 A 20060526
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33845542035
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For the previous synthesis of mackinazolinone 13, see
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For the previous synthesis of mackinazolinone 13, see: W.R. Bowman, M.R. Elsegood, T. Stein, and G.W. Weaver Org. Biomol. Chem. 5 2007 103 113
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A. Kamal, A.V. Ramana, K.S. Reddy, K.V. Ramana, A.H. Babu, and B.R. Prasad Tetrahedron Lett. 45 2004 8187 8190
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Prasad, B.R.6
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