90236-61-6Relevant articles and documents
31P NMR SPECTROSCOPY STUDIES ON THE DIORGANYL PHOSPHOROCHLORIDATE/PYRIDINE PHOSPHORYLATION PROCEDURE
Perich, John W.,Alewood, Paul F.,Johns, R. B.
, p. 1 - 10 (2007/10/03)
The interaction of diphenyl phosphorochloridate and three dialkyl phosphorohloridates (alkyl = Et, Me, Bzl) with pyridine was shown by 31P NMR spectroscopy to lead to the formation of diorganyl phosphoropyridinium ihetrmediate.In the case of diethyl, dime
Synthesis of Casein-Related Peptides and Phosphopeptides. V The Efficient Global 'Phosphite-Triester' Phosphorylation of Protected Serine Derivatives and Peptides by Using Dibenzyl or Di-t-butyl N,N-Diethylphosphoramidite.
Perich, John W.,Johns, R. B.
, p. 1623 - 1632 (2007/10/02)
Both dibenzyl N,N-diethylphosphoramidite and di-t-butyl N,N-diethylphosphoramidite are shown to be suitable reagents for the efficient 1H-tetrazole-catalysed 'phosphite-triester' phosphorylation of the protected serine derivative Boc-Ser-OCH2C6H4NO2-p. Bo
Preparation of Nα-(t-Butoxycarbonyl)-O-(dibenzylphosphono)-L-serine
Alewood, Paul F.,Perich, John W.,Johns, R. B.
, p. 429 - 433 (2007/10/02)
The protected phosphoserine synthon Nα-(t-butoxycarbonyl)-O-(dibenzylphosphono)-L-serine was prepared in three steps.Stability studies on the phosphorylating agent dibenzyl phosphorochloridate were performed by 31P n.m.r. spectroscopy.