A racemization test in peptide synthesis using 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM).

Autor: Kunishima M; Faculty of Pharmaceutical Sciences and High Technology Research Center, Kobe Gakuin University, Japan. kunisima@kgu-p.pharm.kobegakuin.ac.jp, Kitao A, Kawachi C, Watanabe Y, Iguchi S, Hioki K, Tani S
Jazyk: angličtina
Zdroj: Chemical & pharmaceutical bulletin [Chem Pharm Bull (Tokyo)] 2002 Apr; Vol. 50 (4), pp. 549-50.
DOI: 10.1248/cpb.50.549
Abstrakt: Racemization of the C-terminal amino acid (Ala) has been studied in various solvents during coupling between 4-methoxybenzyloxycarbonyl (Z(OMe))-Gly-L-Ala-OH and phenylalanine benzyl ester (H-Phe-OBzl) with 4-(4,6-dimethoxy-1,3,5-thiazin-2-yl)-4-methylmorpholinium chloride (DMT-MM). The reaction occurred without substantial racemization in AcOEt, tetrahydrofuran (THF), N,N-dimethylformamide (DMF), CH3CN, and 2-PrOH, while a slight racemization was observed in dimethyl sulfoxide (DMSO), EtOH, and MeOH. The extent of racemization may correlate with the polarity of the solvents.
Databáze: MEDLINE