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Formation and isolation of simple, stable, acyclic di- and tripeptide hemiacetals
- Source :
- Tetrahedron Letters; January 1996, Vol. 37 Issue: 15 p2521-2524, 4p
- Publication Year :
- 1996
-
Abstract
- 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.
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 37
- Issue :
- 15
- Database :
- Supplemental Index
- Journal :
- Tetrahedron Letters
- Publication Type :
- Periodical
- Accession number :
- ejs45812903
- Full Text :
- https://doi.org/10.1016/0040-4039(96)00385-1