Abstract
The acetic acid catalyed reaction of the free amine form of a glycosylated serine ester with amino acids or peptides built-up on a Kaiser-DeGrado polystyrene benzophenone oxime resin affords C-terminal glycopeptides in a fully-protected form suitable for further chemical manipulation.
Original language | English (US) |
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Pages (from-to) | 7019-7022 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 34 |
Issue number | 44 |
DOIs | |
State | Published - Oct 29 1993 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry