A novel method for the facile synthesis of depsipeptides was written by Gilon, Chaim;Klausner, Yakir;Hassner, Alfred. And the article was included in Tetrahedron Letters in 1979.Recommanded Product: 19444-23-6 This article mentions the following:
Depsipeptides were prepared in 90-8% yields by a one pot synthesis involving condensation reaction of N–tert-butoxycarbonyl (BOC) amino acids with benzyl α-hydroxyalkanoates mediated by dicyclohexylcarbodiimide in the presence of 4-(dimethylamino)- or 4-pyrrolidinopyridine in CH2Cl2 at 25°. Thus, BOC-
Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: 19444-23-6
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics