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1
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Merkushev, E.B.1
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b) Y. Sasson, "Formation of Carbon-Halogen Bonds (CI, Br, I)," in "The Chemistry of Halides, Pseudo-Halides, and Azides, Supplement D1," ed by S. Patai and Z. Rappoport, Wiley-Interscience, Chichester (1995), pp. 535-620;
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Halobenzenes
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P. G. Steel, "Halobenzenes," in "Rodd's Chem. Carbon Compds.," 2nd ed, ed by M. Sainsburry, Elsevier, Amsterdam (1996), Vol. 3, Part 1, pp. 178-224;
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Christie, S.D.R.1
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In its Refs. 1, 2, 3, and 4 there is a list of the former reviews and papers dealing with the aromatic iodination
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B. Krassowska-Świebocka, P. Luliński, and L. Skulski, Synthesis, 1995, 926. In its Refs. 1, 2, 3, and 4 there is a list of the former reviews and papers dealing with the aromatic iodination.
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Luliński, P.2
Skulski, L.3
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Reagents in Organic Synthesis
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N. V. Lazarev, "Khimicheski vrednye veshchestva v promyshlennosti," Goskhimizdat, Leningrad-Moscow (1951); Polish transl., "Szkodliwe substancje w przemyśle," Państw. Wydawn. Techn., Warsaw (1956).
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W. Czerska, M. J. Malawski, and J. Surowiński, "Vademecum drogisty. Substancje nieorganiczne," Vol. I, Biuro Wyd. CHPCh "Chemia," Wyd. Katalogów i Cenników, Warsaw (1966).
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31
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85038194469
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note
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We observed that this preparatory stirring period (2 h, room temperature) was indispensable to attain the high yields given in the Table 1. Presumably, transient iodine(I) and, particularly, iodine(III) species are formed all not at once, but they need some definite time to get possibly highest concentration levels.
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34
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85038197762
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note
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4 had to be added to increase the concentration of transient iodine(I) or iodine(III) species formed in the reaction mixtures.
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35
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0003446724
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Chapman & Hall, London-Glasgow-Weinheim-New York-Tokyo-Melbourne-Madras
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"Dictionary of Organic Compounds," 6th Ed
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