Efficient Stereoselective Synthesis of γ-N-Glycosyl Asparagines by N-Glycosylation of Primary Amide Groups
- 22 January 2005
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 127 (6) , 1630-1631
- https://doi.org/10.1021/ja0450298
Abstract
The efficient and elegant synthesis of N-glycosides by N-glycosylation of asparagine-containing peptides is described. Glycosylation of primary amides with glycosyl N-phenyltrifluoroimidates in the presence of a catalytic amount of TMSOTf in nitromethane smoothly proceeded to provide the corresponding N-glycosyl amino acids in excellent yields. This coupling method was adaptable to the coupling of various glycosyl donors with amino acids and peptides.Keywords
This publication has 4 references indexed in Scilit:
- Glycosylation with N-Troc-protected glycosyl donorsCarbohydrate Research, 1996
- Intramolecular fluorescence enhancement: a continuous assay of Ras farnesyl:protein transferaseJournal of the American Chemical Society, 1992
- Glycosylation of unreactive substratesJournal of the American Chemical Society, 1989
- Carbon-13 nuclear magnetic resonance spectroscopy of naturally occurring substances. XXXI. Carbon-13 nuclear magnetic resonance spectral analysis of quassinoid bitter principlesThe Journal of Organic Chemistry, 1975