524-49-2Relevant articles and documents
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Freedman,Doak
, p. 238 (1956)
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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.
GAS-PHASE PYROLYSIS OF TERVALENT PHOSPHORUS-OXY AND -THIA HETEROCYCLES: A NEW APPROACH TO SHORT-LIVED PENTAVALENT PHOSPHORUS COMPOUNDS HAVING CO-ORDINATION NUMBER 3
Cadogan, J. I. G.,Bracher, Simon,Gosney, Ian,Yaslak, Salih
, p. 229 - 232 (2007/10/02)
Generation of short-lived metaphosphonates by thermal fragmentation of cyclic phosphonites and their thia-analogues in the gas phase is described, including an elaboration of the method whereby a monomeric phosphonobenzene is detected unambiguously for the first time by an intra-molecular trapping reaction which also illustrates the considerable potential of such species in the synthesis of phosphorus heterocycles.