
Bioorganic and Medicinal Chemistry Letters p. 2007 - 2012 (1996)
Update date:2022-08-04
Topics:
Noort
Platenburg
Benschop
Solid phase synthesis of peptides containing a serine thiodiglycol phosphate residue has been achieved by following a global on-resin phosphorylation strategy with a functionalized benzyl phosphoramidite. To preclude cleavage of the acid labile thiodiglycol phosphate ester during deprotection, the thioether functionality was temporarily protected as a sulfoxide.
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