By A.R. Katritzky, A.J. Boulton (Eds.)
(from preface)The 9th quantity of Advances in Heterocyclic Chemistry comprises 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 as a result of the Editorial Board, the writer, and the authors for his or her cooperation.
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Extra resources for Advances in Heterocyclic Chemistry, Vol. 9
D. Popp, and A. C. Heterocyclic Chem. 3 , 9 9 (1966). F. D. Popp, H. W. Gibson, and A. C. Noble, J . Org. Chena. 31, 2296 (1966). 31 J. M. D. Dissertation, Clarkson College of Technology (1967). 32 J. M.. Wefer and F. D. Popp, J . Org. Chem. 32, 1999 (1967). 33 L. R. Welters, N. T. Iyer, and W. E. McEwen, J . A m . Chem. SOC. 80, 1177 (1958). 111. 1 13 REISSERT COMPOUNDS 0 qN 0 m - o - ( ! - C6H5 c6H5 H-C-0-C- I1 C6H5 I CBH5 (30) (29) benzene34 or sodium hydride in dimethylformamide a t room temperaturez7)gave 30.
G. Podrebarac and W. 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.
40, 864 (1962). 45 A. H. Kelly, D. H. McLeod, and J. Parrick, Can. J . Chem. 43, 296 (1965). 46 A. H. Kelly and J. Parrick, Can. J . Chem. 44, 2455 (1966). 47 L. N. Yakhontov, E. V. Pronina, and M. V. Rubtsov, Dokl. Akad. Nauk SSSR 169, 361 (1966); R o c . A c d . Sci. USSR, Chem. Sect. ) 44 169, 705 (1966). Deutsche Gold- und Silver-Scheideanstalt vorm. Roessler, British Patent 259,982 (1925); Chem. Zentr. 991, 2311 (1928). Curiously, this patent does not appear to have been abstracted by Chem.
Advances in Heterocyclic Chemistry, Vol. 9 by A.R. Katritzky, A.J. Boulton (Eds.)