Regio- and stereoselective hydroxylation of some nitrogen heterocyclic compounds by microorganisms was written by Zefirov, N. S.;Terent’ev, P. B.;Modyanova, L. V.;Dovgilevich, E. V.. And the article was included in Indian Journal of Chemistry in 1993.Formula: C7H9NO This article mentions the following:
Microbial hydroxylation of pyridine and alkylpyridines, as well as of some saturated monocyclic compounds, provides an efficient regio- and stereoselective route to biol. active and synthetically useful hydroxy derivatives Thus, the picolines I (R = 2-, 3-, 4-Me) are converted by fungi, such as Aspergillus and Penicillium, into the corresponding pyridinemethanols I (R = 2-, 3-, 4-CH2OH) in up to 45% yields. Transformation of condensed polycyclic N-heterocycles, however proceeds in a different manner. In the experiment, the researchers used many compounds, for example, 6-Methyl-2-pyridinemethanol (cas: 1122-71-0Formula: C7H9NO).
6-Methyl-2-pyridinemethanol (cas: 1122-71-0) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Formula: C7H9NO
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts