1111-92-8Relevant articles and documents
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Burg,A.B.,Slota,P.J.
, p. 2145 - 2148 (1960)
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METHYLPHOSPHINYL (Dmp): A NEW PROTECTING GROUP OF TYROSINE SUITABLE FOR PEPTIDE SYNTHESIS BY USE OF BOC-AMINO ACIDS
Ueki, Masaaki,Sano, Yoshiyuki,Sori, Ichiro,Shinozaki, Kozo,Oyamada,Hidekazu,Ikeda, Shigeru
, p. 4181 - 4184 (2007/10/02)
Use of dimethylphosphinyl (Dmp) group as a side-chain phenolic OH protecting group of tyrosine in peptide synthesis was studied.The Dmp group is resistant to trifluoroacetic acid and hydrogenolysis and removed by fluoride ion or liquid HF.
Evaluation of Phosphinic Acid Derivatives as Reagents For Amine Protection in Peptide Synthesis
Ramage, Robert,Atrash, Butrus,Hopton, David,Parrot, Maxwell J.
, p. 1217 - 1226 (2007/10/02)
The results of a kinetic study of the acid-catalysed methanolysis of a series of N-(2-phenyl-ethyl)phosphinamides incorporating selected substituents on phosphorus have been evaluated in order to define the optimum reagent and conditions for amine protection of α-amino acids during peptide synthesis.