Synthetic Route of 169048-83-3, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 169048-83-3, Name is (S)-5-(Chloromethyl)oxazolidin-2-one, molecular formula is C4H6ClNO2. In a Article£¬once mentioned of 169048-83-3
Electrogenerated chiral building blocks for diastereoselective amidoalkylation reactions
Three different electrochemical methods have been applied for the synthesis of chiral building blocks for diastereoselective amidoalkylation reactions. These are A. the direct anodic alpha-methoxylation of amides and carbamates; B. anodic methoxylative decarboxylation of alpha-amino acid derivatives (Hofer-Moest reaction) C. indirect NaCl mediated anodic alpha-methoxylation of alpha-amino acid derivatives. The application of these building blocks for the synthesis of enantiomerically pure alpha-amino acids, dichiral 1,2-amino alcohols and chiral 1,3-diamines is described.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 169048-83-3. In my other articles, you can also check out more blogs about 169048-83-3
Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H1392NO – PubChem