Download Advances in Heterocyclic Chemistry, Vol. 9 by A.R. Katritzky, A.J. Boulton (Eds.) PDF

By A.R. Katritzky, A.J. Boulton (Eds.)

ISBN-10: 0120206099

ISBN-13: 9780120206094

(from preface)The 9th quantity of Advances in Heterocyclic Chemistry contains surveys of the chemistry of the subsequent teams of heterocyclic compounds: 1,2,5-thiadiazoles (L. M. Weinstock and P. I. Pollack); 1,3,4-thiadiazoles (J. Sandstrom); pyridazines (M. Tisler and B. Stanovnik); Reissert compounds (F. D. Popp); phenothiazines (C. Bodea and that i. Silberg); and pyrrolopyridines (R. E. Willette).Suggestions are welcomed for contributions to destiny volumes; they need to be within the type of brief synopses.Thanks are end result of the Editorial Board, the writer, and the authors for his or her cooperation.

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Extra info for Advances in Heterocyclic Chemistry, Vol. 9

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Curiously, this patent does not appear to have been abstracted by Chem. Abstr. However, all the compounds, except the azaindoles, did appear in French Patent 641,422 (1926) ; Chem. Abstr. 23, 1139 (1929). 49 T. Takahashi, H. Saikachi, H. Goto, and S. Shimamura, J . Pharm. SOC. Japan 64, 7 (1944); Chem. Abstr. 45, 8529 (1951). 4 9 a P . A. Crooks and B. & Ind. (London), 547 (1967). 50 G. E. Ficken and J. D. Kendall, J . Chem. , 3202 (1959). 5 1 G. E. Ficken and J. D. Kendall, J . Chem. , 584 (1961).

E. MoEwen,J. Org. Chem. 26, 1165 (1961). 38 H. W. Gibson, F. D. Popp, and A. Catala, J. Heterocyclic Chem. 1,251 (1964). 39 F. D. Popp and W. E. McEwen, J . Am. Chem. SOC. 80, 1181 (1958). 111. 4. F. D. 29-30 This advantage was noted despite the need of additional synthetic steps to convert the carbinol ester to a methylene group. 37I n the quinoline series the product has been converted to a compound having curariform activity. 33It should be pointed out, however, that the expected tertiary alcohols are available by reaction of Grignard reagents with Reissert compounds as noted below.

Okuda and M. M. Robison, J. Org. Chem. 24, 1008 (1959). 1 9 E. Koenigs and A. Fulde, Chem. Bey. 60, 2106 (1927). 20 W. Herz and D. R. K. Murty, J. Org. Chem. 25, 2242 (1960). 20a M. Hooper, D. A. Patterson, and D. 0. Wibberley, J. Pharm. Pharmacol. 17, 734 (1965). 21 G. R. Clemo and G. A. Swan, J. Chem. , 603 (1945). 22 M. M. Robison and B. L. Robison, J. Am. Chem. SOC. 77,457 (1955). 23 A. Albert and R. E. Willette, J. Chem. , 4063 (1964). 24 R. E. Willette, unpublished results (1966). 13 G. 14 SEC.

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