Formation and isolation of simple, stable, acyclic di- and tripeptide hemiacetals

DOI: 10.1016/0040-4039(96)00385-1

Source and publish data:

Tetrahedron Letters p. 2521 - 2524 (1996)

Update date:2022-08-11

Topics:

Authors:

Miller, John F.

Spaltenstein, Andrew

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Article abstract of DOI:10.1016/0040-4039(96)00385-1

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.

Full text of DOI:10.1016/0040-4039(96)00385-1

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