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π-Electron structures and reactivities of 2,3- and 2,5-dihydroxypyridines

✍ Scribed by V. T. Grachev; B. E. Zaitsev; K. M. Dyumaev; L. D. Smirnov; M. R. Avezov


Book ID
112329492
Publisher
Springer US
Year
1973
Tongue
English
Weight
265 KB
Volume
9
Category
Article
ISSN
0009-3122

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The acylation and carbomethoxylation of 2-methylindolizine were studied. In most cases minor amounts of the 1-substituted isomers were isolated in addition to the "usual" products of substitution in the 3 position. The data from the PMR and mass spectra of the 2-methyl-3-and l-acylindolizines obtain