Synthesis and structural studies of asparagine-modified 2-deoxy-alpha-N-glycopeptides associated with the renin-angiotensin system.


Following addition of N-iodosuccinimide to glycals, reductive hydrogenolysis and ring opening gave 2-deoxy-alpha-N-glycopeptides carrying a deaminated asparagine unit. This reaction could be performed employing glucal, galactal, L-rhamnal, L-fucal and lactal to give the corresponding glycoconjugate building blocks 11, 12, 17, 22, 27 and 32. Further NIS… (More)


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