Benedetti, F. et al. published their research in Tetrahedron Letters in 2000 | CAS: 155975-19-2

tert-Butyl ((1R,2R)-2-hydroxycyclohexyl)carbamate (cas: 155975-19-2) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Synthetic Route of C11H21NO3

Facile inversion of configuration of N-Boc β-amino alcohols via SN2 cyclization to oxazolidinones was written by Benedetti, F.;Norbedo, S.. And the article was included in Tetrahedron Letters in 2000.Synthetic Route of C11H21NO3 This article mentions the following:

Oxazolidinones are obtained by the cyclization of mesylates derived from N-Boc β-amino alcs. Hydrolysis of the N-(tert-butoxycarbonyl)oxazolidinones regenerates the protected amino alcs. with inverted configuration at the OH group. In the experiment, the researchers used many compounds, for example, tert-Butyl ((1R,2R)-2-hydroxycyclohexyl)carbamate (cas: 155975-19-2Synthetic Route of C11H21NO3).

tert-Butyl ((1R,2R)-2-hydroxycyclohexyl)carbamate (cas: 155975-19-2) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Synthetic Route of C11H21NO3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts