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Gronowitz, S.1
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2
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85082941442
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Saito, K.1
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M. A. Perez, J. L. Soto, F. Guzman, and A. Diaz, Synthesis, 1045 (1984).
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Soto, J.L.2
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Diaz, A.4
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10
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0023123974
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E. Lunt, C. G. Newton, C. Smith, G. P. Stevens, M. F. G. Stevens, C. G. Straw, R. J. A. Walsh, P. J. Warren, C. Fizames, F. Lavelle, S. P. Langdon, and L. M. Vickers, J. Med. Chem., 30, 357 (1987).
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Lunt, E.1
Newton, C.G.2
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Stevens, M.F.G.5
Straw, C.G.6
Walsh, R.J.A.7
Warren, P.J.8
Fizames, C.9
Lavelle, F.10
Langdon, S.P.11
Vickers, L.M.12
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11
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85038166925
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note
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Attempted acylation of the title compounds by preforming the amino anion with strong base (e.g, sodium hydride, potassium t-butoxide) was not investigated.
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12
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85038163351
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note
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Upon review of Chemical Abstracts, this thieno[3,4-b]-[1,4]benzothiazepine apparently represents a novel ring system.
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14
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25344442690
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German Patent 1,141,487; 20 Dec 1962
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A. van Schoor, W. Schumann, S. Lust and H. Flemming, German Patent 1,141,487; 20 Dec 1962; Chem. Abstr., 58, 12470g (1963).
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Van Schoor, A.1
Schumann, W.2
Lust, S.3
Flemming, H.4
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17
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0345551864
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R. Dijkstra and H. J. Backer, Rec. Trav. Chim., 73, 569 (1954). Chem. Abstr., 49, 11539h (1955).
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Chem. Abstr.
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21
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0345120554
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John Wiley & Sons, New York
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M. T. Bogert and A. Stull, Org. Synth., Vol VIII, John Wiley & Sons, New York, 1928, p 64.
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Org. Synth.
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Bogert, M.T.1
Stull, A.2
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22
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85038164721
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note
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The glucose reduction of 2-nitrophenyl disulfide has previously been described [23]; however, in our hands, the procedure gave only a limited amount of the expected sodium sulfide, with recovery of starting material predominating. Described here is our modification of the literature procedure.
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23
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84965053650
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F. Gialdi and A. Baruffini, Farmaco, Ed. Sci., 12, 206 (1957); Chem. Abstr., 51, 12850a (1957).
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Farmaco, Ed. Sci.
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Gialdi, F.1
Baruffini, A.2
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24
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84965053650
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F. Gialdi and A. Baruffini, Farmaco, Ed. Sci., 12, 206 (1957); Chem. Abstr., 51, 12850a (1957).
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Chem. Abstr.
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26
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85038165835
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G. Traverso and C. B. Riolo, Ann. Chem., 45, 668 (1955); Chem. Abstr., 50, 5634h (1956).
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Chem. Abstr.
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27
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0344258091
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V. M. Rodionov, B. M. Gogoslovskii, and Z. S. Kazakova, Izvest. Akad. Nauk S.S.S.R., Otdel Khim. Nauk, 536 (1948); Chem. Abstr., 43, 2201b (1949).
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Izvest. Akad. Nauk S.S.S.R., Otdel Khim. Nauk
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Rodionov, V.M.1
Gogoslovskii, B.M.2
Kazakova, Z.S.3
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28
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85038163142
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V. M. Rodionov, B. M. Gogoslovskii, and Z. S. Kazakova, Izvest. Akad. Nauk S.S.S.R., Otdel Khim. Nauk, 536 (1948); Chem. Abstr., 43, 2201b (1949).
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Chem. Abstr.
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29
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85038156738
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Attempted Fischer esterification (methanol, p-toluenesulfonic acid, reflux, 24 hours) of the ortho-substituted benzoic acid was unsuccessful
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Attempted Fischer esterification (methanol, p-toluenesulfonic acid, reflux, 24 hours) of the ortho-substituted benzoic acid was unsuccessful.
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30
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85038171143
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[10] also found a 3-methylacrylonitrile derivative to exist as a mixture of isomers with a similarly broad melting point
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Perez, et al. [10] also found a 3-methylacrylonitrile derivative to exist as a mixture of isomers with a similarly broad melting point.
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Perez1
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