193140-98-6Relevant articles and documents
Efficient synthesis of O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-serine and -threonine building blocks for glycopeptide formation
Saha, Uttam K.,Schmidt, Richard R.
, p. 1855 - 1860 (2007/10/03)
Glucosamine donors 1-3 having N-TCP, N,N-diacetyl and N-Teoc protection, respectively, give with Nα-Boc-protected serine and threonine benzyl esters 4a,b as acceptors exclusively the β-glycosides; they can be transformed into O-GIcNAc serine and threonine derivatives 8a,b. The high yielding O-glycosylation of compounds 4a,b with trichloroacetimidate 3 and the ease of replacement of the N-Teoc group by the N-acetyl group prompted the use of Nα-Fmoc-protected serine and threonine allyl (9a,b) and Pfp active esters (12a,b) as acceptors, thus very efficiently yielding the corresponding O-(N,O-acetylglucosamino) serine and threonine derivatives 11a.b and 14a,b as active esters.
