By A.R. Katritzky, A.J. Boulton (Eds.)
(from preface)The current quantity incorporates a wide selection of heterocyclic chemistry. Syntheses of heterocycles from thioureas are reviewed by way of T. S. Griffin, T. S. Woods, and I). L. Klayman, whereas eight. W. Schneller describes the chemistry of benzothiins and their derivatives (thiochromans. thiochromones, and thio-chromanones). advancements in chrom-3-ene chemistry are reviewed by way of L. Merlini. F. D. Popp contributes a bankruptcy at the isatins. A dialogue of theoretical features of the tautomerism of pyrimidines, by way of J. S. Kwiatkowski and B. Pullman, follows up a corresponding previous contribution (Vol. thirteen) on tautomeric purines. within the ultimate bankruptcy P. and D. Cagniant describe the usual prevalence ami synthesis of the bcnzofurans.
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Additional resources for Advances in Heterocyclic Chemistry, Vol. 18
Example text
Popp, unpuhlishrd rrsiilts. 482 46 [Sec. A FRANK D . ^^^ methyl acetiinidate CH,C( = NH)OCH,,492 lactonitrile and d i b e n ~ y l a m i n e ,2-methyl~~~ ~ y r i d i n e ,and ~ ~ ~ 4-alkylpyridines 494a gave 172-175, respectively. Although active methylene compounds generally give rise to isatylidene derivatives, diethyl malonate 495 and ethyl ~ y a n o a c e t a t e have l ~ ~ been reported to give 3-substituted-3-hydroxyoxindoles. 232*497-500 Use of an excess of phenylmagnesium bromide with N - b e n ~ y l and ~~l G .
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