84449-07-0Relevant articles and documents
OXYDATION OF BENZYLOXYCARBONYL THREONINE AND SERINE METHYL ESTERS TO AN OXAMATE DERIVATIVE
Stachulski, Andrew V.
, p. 3789 - 3790 (1982)
Both benzyloxycarbonyl threonine and serine methyl esters, when subjected to oxidation with reagents based on chromium(VI) oxide, gave rise to the same N-protected methyl oxamate, whose structure was confirmed by independent preparation.
Oxidation of threonine residues with IBX reagents
Abeysinghe, P. Manohari,Han, Yu,Harding, Margaret M.
experimental part, p. 2601 - 2604 (2009/08/09)
The treatment of protected Thr peptides with excess polymer-bound IBX effects sequential oxidation of the Thr secondary alcohol to the ketone, followed by hydroxylation of the alpha carbon of the Thr residues with loss of stereochemistry at this position.