Pentafluorophenyl esters for the temporary protection of the α-carboxy group in solid phase glycopeptide synthesis
- 1 January 1990
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 6,p. 483-485
- https://doi.org/10.1039/c39900000483
Abstract
The pentafluorophenyl ester of fluoren-9-ylmethoxycarbonyl serine was found to be stable to glycosylation conditions and the purified glycosylation product was easily incorporated into a solid phase assembly of a nonapeptide analogue of the antifreeze glycopeptides.Keywords
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