Formation and isolation of simple, stable, acyclic di- and tripeptide hemiacetals
Di- and tripeptide aldehydes were found to undergo reaction with methanol to afford the corresponding methyl hemiacetals. These compounds, which possessed unusual stability, were isolated and characterized using NMR techniques and a chemical correlation experiment.
Miller, John F.,Spaltenstein, Andrew
p. 2521 - 2524
(2007/10/03)
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