《Organocatalytic multicomponent synthesis of α/β-dipeptide derivatives》 was published in Chemistry – A European Journal in 2020. These research results belong to Martzel, Thomas; Annibaletto, Julien; Millet, Pierre; Pair, Etienne; Sanselme, Morgane; Oudeyer, Sylvain; Levacher, Vincent; Briere, Jean-Francois. SDS of cas: 60656-87-3 The article mentions the following:
A straightforward multicomponent Knoevenagel-aza-Michael-cyclocondensation reaction involving readily available hydroxamic acid-derived from naturally occurring α-amino acids allows a diversity-oriented synthesis of novel isoxazolidin-5-ones possessing an N-protected α-amino acid pendant with good to high diastereoselectivities thanks to a match effect with a chiral organocatalyst. These diversely substituted heterocycles, easily isolated as a single diastereoisomer, proved to be versatile platforms for the formation of an array of α/β-dipeptide fragments. The experimental part of the paper was very detailed, including the reaction process of 2-(Benzyloxy)acetaldehyde(cas: 60656-87-3SDS of cas: 60656-87-3)
2-(Benzyloxy)acetaldehyde(cas: 60656-87-3) may be used in the following syntheses: (3S,5S)-methyl 6-benzyloxy-3,5-dihydroxyhexanoate ,(S)-5-benzyloxy-4-hydroxypentan-2-one, myxothiazols.SDS of cas: 60656-87-3
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem