Quesnel A, Briand J P
Moléculaire et Cellulaire, UPR 9021-CNRS, Strasbourg, France.
J Pept Res. 1998 Aug;52(2):107-11. doi: 10.1111/j.1399-3011.1998.tb01364.x.
During the Fmoc solid-phase synthesis of reduced peptide bond analogues, we observed that the trityl protection of an asparagine residue in the vicinity of a reduced peptide bond is not cleaved completely after the final trifluoroacetic acid deprotection step. The relative position of the Asn side-chain amine and of the aminomethylene bond as well as the preferential protonation of the secondary amine can be used to explain this phenomenon. We show that longer deprotection times or the use of methyl-trityl protection partially improves the yield of the Asn-deprotected peptide whereas xanthenyl protection totally overcomes this problem.
在还原肽键类似物的Fmoc固相合成过程中,我们观察到,在最终的三氟乙酸脱保护步骤后,还原肽键附近天冬酰胺残基的三苯甲基保护并未完全裂解。天冬酰胺侧链胺和氨亚甲基键的相对位置以及仲胺的优先质子化可用于解释这一现象。我们表明,延长脱保护时间或使用甲基三苯甲基保护可部分提高天冬酰胺脱保护肽的产率,而呫吨基保护则完全克服了这一问题。