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.Category: alcohols-buliding-blocks 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, (5-Methylpyridin-3-yl)methanol (cas: 102074-19-1Category: alcohols-buliding-blocks).
(5-Methylpyridin-3-yl)methanol (cas: 102074-19-1) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Category: alcohols-buliding-blocks
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts