Category: 813433-76-0

Pousset, Cyrille; Callens, Roland; Marinetti, Angela; Larcheveque, Marc published their research in Synlett on December 7 ,2004. The article was titled 《An efficient synthesis of chiral cyclic β-amino acids via asymmetric hydrogenation》.Related Products of 813433-76-0 The article contains the following contents:

Cyclic β-amino acids homoproline, homopipecolic acid and 3-(carboxymethyl)morpholine were obtained in high enantiomeric excesses by transition metal-catalyzed asym. hydrogenation of cyclic β-acylamino alkenoates. These compounds were synthesized by a thio-Wittig reaction on N-protected thiolactams. The experimental process involved the reaction of (S)-tert-Butyl 3-(2-hydroxyethyl)morpholine-4-carboxylate(cas: 813433-76-0Related Products of 813433-76-0)

(S)-tert-Butyl 3-(2-hydroxyethyl)morpholine-4-carboxylate(cas: 813433-76-0) belongs to esters.Related Products of 813433-76-0 They are important in biology, being one of the main classes of lipids and comprising the bulk of animal fats and vegetable oils.Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones.

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Fustero, Santos; Jimenez, Diego; Moscardo, Javier; Catalan, Silvia; del Pozo, Carlos published their research in Organic Letters on December 6 ,2007. The article was titled 《Enantioselective Organocatalytic Intramolecular Aza-Michael Reaction: a Concise Synthesis of (+)-Sedamine, (+)-Allosedamine, and (+)-Coniineã€?HPLC of Formula: 813433-76-0 The article contains the following contents:

The intramol. aza-Michael reaction of carbamates bearing remote α,β-unsaturated aldehydes under organocatalytic conditions took place with good yields and excellent ee’s when Jorgensen catalyst was used in the process, giving rise to the enantioselective formation of several five- and six-membered heterocycles. The developed methodol. was applied to the synthesis of three piperidine alkaloids I, II and III. The results came from multiple reactions, including the reaction of (S)-tert-Butyl 3-(2-hydroxyethyl)morpholine-4-carboxylate(cas: 813433-76-0HPLC of Formula: 813433-76-0)

(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.Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones.HPLC of Formula: 813433-76-0

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

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