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31444443942
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more..
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14
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31444452200
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U.S. Patent 5,654,305, 1997;
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31444440668
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U.S. Patent 5,567,711, 1996;
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19
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31444434244
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-
For a discussion, see Ref. 2, pp 39-41.
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For a discussion, see Ref. 2, pp 39-41.
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-
-
-
21
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1942460740
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For an extension of this excellent procedure to the synthesis of 1-phenylsulfonyl-1H-pyrroles, see also: (b) R.X. Xu, H.J. Anderson, N.J. Gogan, C.E. Loader, and R. McDonald Tetrahedron Lett. 22 1981 4899 4900
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Xu, R.X.1
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McDonald, R.5
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23
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31444443393
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-
note
-
The crystallographic data (excluding structure factors) for compound 8a have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 281814. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk ].
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24
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0001383512
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See, for example: (a) J. Rokach, P. Hamel, M. Kakushima, and G.M. Smith Tetrahedron Lett. 22 1981 4901 4904
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Rokach, J.1
Hamel, P.2
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Smith, G.M.4
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26
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37049074651
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R.L. Beddoes, L. Dalton, J.A. Joule, O.S. Mills, J.D. Street, and C.I.F. Watt J. Chem. Soc., Perkin Trans. 2 1986 787 797
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Dalton, L.2
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Mills, O.S.4
Street, J.D.5
Watt, C.I.F.6
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28
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0036859011
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Although no spectral or physical data were given, this compound has previously been obtained in 92% yield by reaction of indole with NaH in DMF, followed by treatment with benzenesulfonyl chloride, see: T. Sasaki, Y. Igarashi, M. Ogawa, and T. Furumai J. Antibiot. 55 2002 1009 1012
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Sasaki, T.1
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Furumai, T.4
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29
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31444443680
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Ph.D. Thesis, Dartmouth College, Hanover, NH
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2 as the solvent, see: Davis, D. A. Ph.D. Thesis, Dartmouth College, Hanover, NH, 1990.
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(1990)
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Davis, D.A.1
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35
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31444452741
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WO Patent Appl. 03/013510, 2003;
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WO Patent Appl. 03/013510, 2003; Chem. Abstr. 2003, 138, 187788.
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