148616-42-6Relevant articles and documents
Formation of diphosphates. A NMR study on the mechanism and stereochemistry of diphosphate formation from chiral dioxaphosphorinanes
Hulst, Ron,Visser, Johanna M.,De Vries, N. Koen,Zijlstra, Robert W. J.,Kooijman, Huub,Smeets, Wilberth,Spek, Anthony L.,Feringa, Ben L.
, p. 3135 - 3150 (2000)
During the use of chiral 2-oxo-1,3,2-dioxaphosphorinanes as derivatizing reagents in the enantiomeric excess determination of amines, alcohols, and unprotected amino acids, minor traces of side reaction products were observed by 1H and 31
(S)-2H-2-oxo-5,5-dimethyl-4(R)-phenyl-1,3,2-dioxaphosphorinane, a New Reagent for the Enantiomeric Excess Determination of Unprotected Amino Acids using 31P NMR
Hulst, Ron,Zijlstra, Robert W. J.,Vries, N. Koen de,Feringa, Ben L.
, p. 1701 - 1710 (2007/10/02)
Diastereomeric amide derivatives of title phosphorinane 2 and unprotected amino acids are easily prepared in aqueous solutions, showing well separated signals in the 31P NMR spectra allowing accurate e.e. determination.