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

ISBN-10: 0120206110

ISBN-13: 9780120206117

(from preface)This, the 11th quantity of Advances in Heterocyclic Chemistry, comprises surveys of the chemistry of the subsequent teams of heterocyclic compounds: benzo[6]thiophenes (B. Iddon and R. M. Scrow-ston), naphthyridines (W. W. Paudler and T. J. Kress), and quinu-clidines (L. N. Yakhontov). additionally, R. A. Jones covers the appliance of actual ways to pyrrole chemistry and a truly topical topic, the photochemistry of heterocycles, is reviewed via S. T. Reid.Suggestions are welcomed for contributions to destiny volumes; they need to be within the type of brief sj'nopses.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. 11

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King, P. de Mayo, E. Morkved, A. B. M. A. Sattar, and A. Stoessl, Can. J . Chem. 41, 100 (1963). E. S. T. REID derivative (133). Recent studies lZ2 using flash photolysis have cast doubt on the existence of an intermediate sulfene (134). I (132) (134) (133) Irradiation of an N-substituted sultam yieldslZ3the correspondingly substituted pyrrole; this has been interpreted as arising by nucleophilic attack of nitrogen on an intermediate sulfene [Eq. (32)]. The formation l Z 4of a pyrrole by irradiation of dimethyl-l,2-dihydropyridazine- 1,2-dicarboxylate in ether is also thought to involve initial ring cleavage [Eq.

Am. Chem. SOC. 88, 5931 (1966). 119 R. Exelby and R. Grinter, Chem. Rev. 65, 247 (1965). Hirshberg, and E. Fischer, J . Chem. SOC. 156 (1961). 1 2 1 J. King, P. de Mayo, E. Morkved, A. B. M. A. Sattar, and A. Stoessl, Can. J . Chem. 41, 100 (1963). E. S. T. REID derivative (133). Recent studies lZ2 using flash photolysis have cast doubt on the existence of an intermediate sulfene (134). I (132) (134) (133) Irradiation of an N-substituted sultam yieldslZ3the correspondingly substituted pyrrole; this has been interpreted as arising by nucleophilic attack of nitrogen on an intermediate sulfene [Eq.

SOC. 84,3736 (1962). T. H. Kinstle, R. L. Welch, and R. W. Exley, J . Am. Chem. 89, 3660 (1967). P. G. Gassman and K. T. Mansfield, J . Org. C k m . 32, 915 (1967). 72 K. Kocsis, P. G. Ferrini, D. Arigoni, and 0. Jeger, Helv. Chim. Acta 43,2178 71 (1960). 7 3 M. Franck-Neumann, Tetrahedron Letters 2979 (1968). S. Masamune, H. Zenda, M. Wiesel, N. Nakatsuka, and G. Bigam, J . Am. Chem. SOC. 90, 2727 (1968). 75 T. F. Thomas, C. I. Sutin, and C. Steel, J . Am. Chem. SOC. 89, 5107 (1967). 74 24 5. T.

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