ISSN:
1573-9171
Source:
Springer Online Journal Archives 1860-2000
Topics:
Chemistry and Pharmacology
Notes:
Summary 1. A study was made of the comparative reactivity of the ortho- and para-positions of 3-hydroxypyridine and 6-methyl-3-hydroxypyridine in the aminomethylation reaction. 2. In contrast to phenol,β-pyridinol forms only the 2,6-bis-substituted products, while 6-in ethyl-3-hydroxypyridine forms only the 2-monosubstituted compounds. Substitution in the 4 position was not observed in either case.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1007/BF00854892