Application In Synthesis of (S)-tert-Butyl 3-(2-hydroxyethyl)morpholine-4-carboxylateOn November 1, 2004 ,《Enzymatic resolution of cyclic N-Boc protected β-amino acids》 appeared in Tetrahedron: Asymmetry. The author of the article were Pousset, Cyrille; Callens, Roland; Haddad, Mansour; Larcheveque, Marc. The article conveys some information:
Me and Et esters of N-Boc homoproline, homopipecolic acid and 3-carboxymethyl-morpholine were kinetically resolved by hydrolysis catalyzed by Burkholderia cepacia lipase to give the corresponding acids and residual esters in enantiomeric excesses better than 99% (E >100). After reading the article, we found that the author used (S)-tert-Butyl 3-(2-hydroxyethyl)morpholine-4-carboxylate(cas: 813433-76-0Application In Synthesis of (S)-tert-Butyl 3-(2-hydroxyethyl)morpholine-4-carboxylate)
(S)-tert-Butyl 3-(2-hydroxyethyl)morpholine-4-carboxylate(cas: 813433-76-0) belongs to esters. They are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils. They 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.Application In Synthesis of (S)-tert-Butyl 3-(2-hydroxyethyl)morpholine-4-carboxylate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics