Safety of tert-Butyl ((1S,2S)-2-hydroxycyclohexyl)carbamate. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: tert-Butyl ((1S,2S)-2-hydroxycyclohexyl)carbamate, is researched, Molecular C11H21NO3, CAS is 145166-06-9, about Enzymatic method of preparation of optically active trans-2-amino cyclohexanol derivatives. Author is Ursini, A.; Maragni, P.; Bismara, C.; Tamburini, B..
Supported Lipase Amano PS-D catalyzes the resolution of (±)-trans-2-[(tert-butoxycarbonyl)amino]cyclohexanol by a selective acylation reaction. Using the supported enzyme gave a much faster reaction compared to existing methodol. on similar substrates. A variety of acylating agents were investigated, with vinyl acetate providing the most practical and convenient procedure.
Different reactions of this compound(tert-Butyl ((1S,2S)-2-hydroxycyclohexyl)carbamate)Safety of tert-Butyl ((1S,2S)-2-hydroxycyclohexyl)carbamate require different conditions, so the reaction conditions are very important.
Reference:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem