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EnglishDouble glycosylation of cysteine-containing peptides has been carried out by a one-pot two-step sequence comprising selective S-propargylation followed by photoinduced (λ max 365 nm) free-radical hydrothiolation with glycosyl thiols. Conditions were established for the sequential introduction of two different thiol residues such as a glycosyl and a biotinyl derivative.
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| Data di pubblicazione: | 2010 | |
| Titolo: | Photoinduced addition of glycosyl thiols to alkynyl peptides: use of free-radical thiol-yne coupling for post-translational double-glycosylation of peptides | |
| Autori: | M. Lo Conte; S. Pacifico; A. Chambery; A. Marra; A. Dondoni | |
| Rivista: | JOURNAL OF ORGANIC CHEMISTRY | |
| Abstract: | Double glycosylation of cysteine-containing peptides has been carried out by a one-pot two-step sequence comprising selective S-propargylation followed by photoinduced (λ max 365 nm) free-radical hydrothiolation with glycosyl thiols. Conditions were established for the sequential introduction of two different thiol residues such as a glycosyl and a biotinyl derivative. | |
| Handle: | http://hdl.handle.net/11392/1400985 | |
| Appare nelle tipologie: | 03.1 Articolo su rivista |
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