A convergent synthesis of novel conformationally restricted HIV-1 protease inhibitors was written by Kim, B. Moon;Guare, James P.;Hanifin, Colleen M.;Arford-Bickerstaff, Deborah J.;Vacca, Joseph P.;Ball, Richard G.. And the article was included in Tetrahedron Letters in 1994.Recommanded Product: 87694-53-9 This article mentions the following:
Conformationally restricted HIV-1 protease inhibitors I (m = 1, n = 0; m = 0, n = 1), II, III, and IV, containing the transition state hydroxyl group in pyrrolidine or piperidine ring systems, were synthesized stereoselectivity utilizing the inherent stereochem. of an amino acid derivative A convergent double reductive amination strategy was used to construct the heterocyclic rings. In the experiment, the researchers used many compounds, for example, (S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate (cas: 87694-53-9Recommanded Product: 87694-53-9).
(S)-tert-Butyl (1-(methoxy(methyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate (cas: 87694-53-9) belongs to esters. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Recommanded Product: 87694-53-9
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Ester – an overview | ScienceDirect Topics