Advances in Heterocyclic Chemistry by Alan R. Katritzky

By Alan R. Katritzky

(from preface)Volume forty five of Advances in Heterocyclic Chemistry comprises 5 contributions, all of which holiday new floor for this sequence. within the first article, Fujita and Nagao describe using heterocycles for the induction of chirality. Thiscontribution represents an instance of how within which our topic is making itself more and more felt in the course of the entire box of chemistry. the second one article, by means of Tisler, covers heterocyclic quinones, together with the various sessions during which a heterocycle is fused to a 1,2- or 1,4-benzoquinone ring.In the 3rd article, Porter describes the chemistry of thiophenium salts and ylids, to which he has contributed generally. The chemistry of 1,4-diazocines is gifted by means of Perlmutter; this text follows an prior evaluation by way of a similar writer on azocines in quantity 31 of Advances in Heterocyclic Chemistry. the ultimate article of this quantity, and the second one contribution from Japan, is by means of Tsuge and Kanemasa and bargains with contemporary advances in azomethine ylide chemistry.The cumulative index updates, as introduced within the preface to quantity forty, will disguise Volumes 41-45 and should seem in quantity forty six. this may hinder a hold up within the booklet of quantity forty five.

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Abe, Y. Kuramoto, T. Taga, S. Aoyagi, Y. Nagase, M. Ochiai, Y. Inoue, and E. Fujita, J. Am. Chem. Soc. 108, 4673 (1986). Y. Nagao, Y. Hagiwara, T. Kumagai, M. Ochiai, T. Inoue, K. Hashimoto, and E. Fujita, J. Org. Chem. 51,2391 (1986). Y. Nagao, T. Kumagai, S. Takao, T. Abe, M. Ochiai, Y. Inoue, T. Taga, and E. Fujita, J. Org. Chem. 51, 4737 (1986). Y. Nagao, T. Inoue, Y. Hagiwara, and E. Fujita, unpublished results (1986). Y. Nagao, T. Nakamura, M. Ochiai, K. Fuji, and E. Fujita, J. C. S . Chem.

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1. Chroman- and lsochromandiones . . . . . . . 2. Tricyclic Systems . . . . . . . . . . . a. b]pyran-5. 6-dione . . . . . . . b . IO-dione. Tetracyclic. and Higher Systems . . . . . . . J . 4-Dioxane. 1,4-Dithiane, and 1,4-Oxathiane . . . 1. 1,4-Dioxane Derivatives . . . . . . . . . 2 . 1,4-Dithiane Derivatives . . . . . . . . . 3. 4-Oxathiane Derivatives. . . . . . . . . . . . . . . . . . . . . .

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