Basic carbapenem analogs: synthesis and in vitro activity of 1β-methyl-2-(pyridylmethylthio)-carbapenems was written by Balkovec, James M.;Szymonifka, Michael J.;Heck, James V.;Ratcliffe, Ronald W.. And the article was included in Journal of Antibiotics in 1991.Recommanded Product: 79651-64-2 This article mentions the following:
The title compounds I (R = pyridyl, aminopyridyl) were prepared and demonstrated more potent activity than thienamycin especially against Gram-neg. organisms. The structure-activity relationship of I is also reported. In the experiment, the researchers used many compounds, for example, (6-Aminopyridin-2-yl)methanol (cas: 79651-64-2Recommanded Product: 79651-64-2).
(6-Aminopyridin-2-yl)methanol (cas: 79651-64-2) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Recommanded Product: 79651-64-2
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts