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Download Advances in Heterocyclic Chemistry, Vol. 10 by A. R., & A. J. Boulton (Eds), Katritzky PDF

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

(from preface)The 10th quantity of this serial book includes six chapters, 4 of which take care of the final chemistry of a particular team of heterocyclic compounds: pyridopyrimidines (W. J. Irwin and D. G. Wibberley), benzofuroxans (A. J. Boulton and P. B. Ghosh), isoindolee (J. D. White and M. E. Mann), and pyrylium salts (A. T. Balaban, W. Schroth, and G. Fischer). the remainder chapters are thinking about indole Grignard reagents (R. A. Heacock and S. Kasparek) and with cyclic hydroxamic acids (J. B. Bapat, D, St. C. Black, and R. C. Brown).The overseas taste of the ebook is preserved: our participants come from six nations in 3 continents.We thank the authors and publishers for his or her cooperation which has allowed construction of this quantity in lower than 365 days.

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138 D. Dal Monte Casoni and E. Sandri, Belgian Patent No. 660,379 (1965); Chem. Abstr. 64, 2098 (1966). 130A. [Sec. ] BENZOFUROXANS 31 to its being patented for use in detonators,"' while benzofuroxan has been proposed as a photographic desensitizer, 140 and it and a number of its derivatives have been tested for use as depolarizers in electric cells,'20, 141*142 and as antiskinning agents in drying oil compositions. 143 X. Table of Benzofuroxans The following table lists the benzofuroxan derivatives, with their melting points, which the authors have been able to find in the published literature.

S. Patent No. 3,050,395 (1962);Chem. Abstr. 58, 164 (1963). 1 4 1 W. B. Hardy and R. A. S. Patent No. 3,163,561 (1964); Chem. Abstr. 64, 3559 (1966). 142 J. T. Shew, J. D. Voorhies, and S. M. Davis, French Patent No. 1,374,790 (1964); Chem. Abstr. 62, 7769 (1965). 143 R. H. S. Patent No. 2,630,438 (1953); Chem. Abstr. 47, 5698 (1953). 144 E. Muller and K. Weisbrod, J . Prakt. Chem. Ser. 2, 113, 30 (1926). 145 P. Karrer, Ber. Deut. Chem. Ges. 46, 253 (1913). 146 P. B. Ghosh and M. W. Whitehouse, J .

Obshch. Khim. 24, 1994 (1954); J . Gen. Chem. USSR24, 1989 (1954); Chem. Abstr. 49, 13977 (1955). 110 M. V. Gorelik, in “Organicheskie Poluprodukti i Krasiteli. Vol. 3: Sul’fiovanie Solyami Sernistoi Kisloti-Reaktsii Bogdanova,” pp. 9&119. Khimiya, Moscow, 1965. 106 [Sec. VI. ] 23 BENZOFUROXANS of its derivatives,110-112leading to nitroamines, naphthofurazans, or 1,2-naphthoquinone dioxime derivatives, depending upon the conditions. Curious products isolated by Bailey and Evans from the reaction of benzotrisfuroxan with triphenyl phosphine have been examined by X-ray crystallography by Cameron and Prout.

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