Spectroscopic and kinetic evidence for a cyclic geminal diamine intermediate in the reaction of O-aminoserine with pyridoxal 5′-phosphate in alkali
- 1 December 1981
- journal article
- research article
- Published by Elsevier in Archives of Biochemistry and Biophysics
- Vol. 212 (2) , 581-588
- https://doi.org/10.1016/0003-9861(81)90401-x
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- Equilibriums and absorption spectra of Schiff basesJournal of the American Chemical Society, 1980
- Catalysis of transimination by rate-limiting proton transfer to buffer basesJournal of the American Chemical Society, 1980
- Preparation and Properties ofO-Amino-D-serine; Acid Hydrolysis of D-4-Amino-3-isoxazolidinone (D-Cycloserine)Synthesis, 1980
- A13C NMR study of pyridoxal-5′-phosphate oximeMagnetic Resonance in Chemistry, 1979
- On the mechanism of decomposition of geminal diaminesJournal of the American Chemical Society, 1978
- Studies on the reactions of substituted D,L-erythro-β-phenylserines with lamb liver serine hydroxymethylase. Effects of substituents upon the dealdolization stepBiochemistry, 1977
- Kinetics and equilibriums of the reaction of pyridoxal 5'-phosphate with ethylenediamine to form Schiff bases and cyclic geminal diamines. Evidence for kinetically competent geminal diamine intermediates in transimination sequencesJournal of the American Chemical Society, 1975
- Reaction of amines with pyridoxal azomethines. Transaldimation and its role in the mechanism of vitamin B6 enzymesJournal of the American Chemical Society, 1971
- Studies on the Mechanism of Oxime and Ketimine Formation1Journal of the American Chemical Society, 1966
- Preparation of Crystalline Phosphorylated Derivatives of Vitamin B6Journal of the American Chemical Society, 1954