Department of Chemistry, University at Albany, State University of New York, 1400 Washington Avenue, Albany, New York 12222, United States.
Org Lett. 2021 May 21;23(10):4008-4012. doi: 10.1021/acs.orglett.1c01218. Epub 2021 May 12.
A stereospecific convergent peptide arginine glycosylation method is reported for the first time. A recently discovered arginine glycosylation invigorated the interests of arginine modification, which has been challenging, because of the inertness of the guanidino side chain. The approach renders the arginine glycoside construction convergently. Catalyzed by palladium complex, glycals modify arginine guanidino groups in one step with high functional group tolerance at ambient temperature. The glycosylated products may be converted to glycopeptide analogues in few steps.
本文首次报道了一种立体专一性的、收敛型的多肽精氨酸糖基化方法。由于胍基侧链的惰性,精氨酸的修饰一直具有挑战性,但最近发现的精氨酸糖基化方法激发了人们对其进行修饰的兴趣。该方法可实现精氨酸糖苷的收敛性构建。在钯配合物的催化作用下,糖基在一步反应中即可修饰精氨酸的胍基基团,并且在环境温度下具有很高的官能团容忍度。所得的糖基化产物可通过几步反应转化为糖肽类似物。