Advances in Heterocyclic Chemistry, Vol. 15 by A. R. Katritzky, A. J. Boulton PDF

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By A. R. Katritzky, A. J. Boulton

ISBN-10: 0120206153

ISBN-13: 9780120206155

(from preface)The current quantity comprises seven chapters, 5 of which take care of facets of particular ring platforms: 4-oxy- and 4-keto-l ,2,3,4-tetrahydroiso-quinolines (J. M. Bobbitt), the oxidation items of pyrroles (O. P. Gardini), the pyrindines (4- and 5-azaindenes) (F. Freeman), the NMR spectra of indoles (S. P. Hiremath and R. S. Hosmane), and the 1,2-benzoisothiazole-S-dioxides—(saccharin and its derivatives) (H. Hettler). within the normal box of heterocyclic chemistry, hydrogen trade reactions, almost always on steel surfaces, are handled (G. E. Calf and J. L. Garnett), and the rest bankruptcy is a scientific evaluation of heterocyclic oligomers (A. Albert and H. Yamamoto). the quantity is devoted to Professor Adrien Albert, and this Preface is via a short biography and bibliography.

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Lag Numerous oligosaccharides occur naturally, 170 an example being obtained from amygdalin (~-mandelonitrile-~-g~ucosido-6-~-~-g~ucos~de) For a review, see T. Robinson, “The Biochemistry of Alkaloids,” p. 24. SpringerVerlag, Berlin and New York, 1968. 164 F. Arcamore, F. Bizioli, G. Canevazzi, and A. Grein, German Patent, 1,039,198 (1958); Chern. Abstr. 55, 2012 (1961). 165 F. Arcamore, S. Penco, P. Orezzi, V. Nicolella, and A. Pirelli, Nature (London) 203, 1064 (1964). g. (a)Albert,6* p. 236; (b) J.

Thesing and H. Mayer, Chem. Ber. 89, 2159 (1956). 112 T. Yoshioka, S. Higashida, S. Morimura, and K. Muraysma, Bull. Chem. SOC. ( J u p . )44, 2207 (1971). log 28 [Sec. B. A. ALBERT AND H. YAMAMOTO cyclobutane-type dimer (92)113 formed by solid-state irradiation of /3-( 3-pyridyl)-trans-acrylic acid ; the trans head-to-head configuration of 92 has been interpreted in terms of crystal p a ~ k i n g . " Already ~ in 1937, a similar cyclobutane-type photodimer had been obtained114 from Z-(/I-styryl)quinoline(solid state), although it is still uncertain whether the dimer is head-to-head or head-to-tail.

Acad. , Ser. C 271, 688 (1970); Chem. Abstr. 74, 22667 (1971). 189 198 A.

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Advances in Heterocyclic Chemistry, Vol. 15 by A. R. Katritzky, A. J. Boulton

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