By Alan R. Katritzky
(from preface)Martin Bryce. Jan Becher, and Birgitte Falt-Hansen offer a survey of the habit of thioaldehydes and their seleno and teleuro analogues, and of thionitroso compounds and their seleno analogues, as heterodie-nophiles. this can be a topic which has exploded lately with 3 quarters of the references from the final decade.L.I. Belen'kii and N. D. Kruchkovskaya have up-to-date their survey of the literature of heterocyclic assessment articles. this is often the fourth installment during this sequence: earlier overviews of heterocyclic studies seemed in Volumes 7 (literature as much as 1965), 25 (literature 1966-1978) via S. M. Weeds and P. M. Jones together with your editor, and quantity forty four (literature 1979-1987) by means of L. I. Belen'kii. a specific characteristic of this review is its assurance of the Russian language literature in addition to Western sources.Heinrich Wamhoff and Jorg Dzenis talk about the synthesis, constitution, and reactions of uracils with specific emphasis on their application in heterocyclic synthesis.Finally, S. Arai and M. Hida evaluation polycyclic fragrant nitrogen cations containing bridgehead (ring fusion) nitrogen atoms. The chemistry of quinolizinium salts used to be lined by means of Thyagarajan in quantity five of our sequence again in 1965, and even though different partial experiences can be found, we've got for the 1st time a latest entire therapy.
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Extra resources for Advances in Heterocyclic Chemistry
I . General Sources and 45 46 47 47 41 49 49 50 5I 51 a. General . . . . . . . . . . . . . . 53 e. Indole Alkaloids. . . . . . . 3. Antibiotics . . . . . . . . . . ....... 54 e. Polyether Antibiotics . ..... a. General 6. Pesticides . a. General . . . . . . . . .................... 58 58 LITERATURE O F HETEROCYCLIC CHEMISTRY f. Pheromones and Other Substances from Insects . . . . . . . ......... g. Natural and Synthetic Food Additives h. OtherTopics .
Amination of heterocycles (Chichibabin reaction): 88AHC(44)I . Heterocyclic cations, reactions with aliphatic diazocompounds: 85MI3. Hydroboration of heterocycles: 90JHC13. Netallation of heterocycles: 87MI24, 87MI36; 88MI 14; 90CRV879, 90MI10. Nucleophilic ring opening of saturated heterocycles: 88KGS 1 155. Reactions of heterocycles with sulfur-containing dianions: 88Y2 1. Reduction of heterocycles: 86MI15; 89CRV459. Transition metal activated nucleophilic substitution in heteroaromatic compounds: 90BSF401.
E . Hydropyridines ....................................... f . Biologically Active Pyridines and Hydropyridines . . . . . . . g. Pyridines Annelated with Carbocycles ...................... h . Pyridines Annelated with H 2. One Oxygen Atom . . . . . a . Pyrylium Compounds . . . b . Pyrans and Hydropyrans . . . . . . . . . . . . . . . . c . Spiropyrans . . . . . . . . . . . . . . . . . . . . . d . Annelated Pyrans and Pyrilium Salts .......................
Advances in Heterocyclic Chemistry by Alan R. Katritzky