Permanganate oxidation of 4-thiouracil derivatives. Isolation and properties of 1-substituted-2-pyrimidone-4-sulfonates.

[1]  H. Hayatsu,et al.  Permanganate oxidation of 4-thiouracil derivatives. Isolation and properties of I-substituted 2-pyrimidone 4-sulfonates. , 1970, Biochimica et biophysica acta.

[2]  H. Hayatsu.  The oxygen-catalyzed reaction between 4-thiouridine and sodium sulfite. , 1969, Journal of the American Chemical Society.

[3]  H. Hayatsu,et al.  Studies on the chemical modifications of nucleic acids. The permanganate oxidation of thymine. , 1969, Tetrahedron letters.

[4]  J. R. Fresco,et al.  Chemical transformation of 4-thiouracil nucleosides to uracil and cytosine counterparts. , 1968, Journal of the American Chemical Society.

[5]  K. Scheit.  Über die Synthese und Eigenschaften von 4-Thiouridylyl-(3′-5′)-4-thiouridin, 4-Thiouridylyl-(3′-5′)-uridin und Uridylyl-(3′-5′)-4-thiouridin , 1968 .

[6]  F. Fittler,et al.  N6-(Δ2-isopentenyl)adenosine: Biosynthesis invitro by an enzyme extract from yeast and rat liver , 1968 .

[7]  H. Hayatsu,et al.  The selective degradation of pyrimidines in nucleic acids by permanganate oxidation. , 1967, Biochemical and biophysical research communications.

[8]  K. Burton.  Oxidation of pyrimidine nucleosides and nucleotides by osmium tetroxide. , 1967, The Biochemical journal.

[9]  M. Lipsett.  The isolation of 4-thiouridylic acid from the soluble ribonucleic acid of Escherichia coli. , 1965, The Journal of biological chemistry.

[10]  T. Ueda,et al.  NUCLEOSIDES. XVII. PYRIMIDINYL AMINO ACIDS. , 1963, Journal of medicinal chemistry.

[11]  E. I. Budowsky,et al.  Some synthetic analogues of uridine diphosphate glucose. , 1963, Tetrahedron.

[12]  M. L. Eidinoff,et al.  Thiation of Nucleosides. II. Synthesis of 5-Methyl-2'-deoxycytidine and Related Pyrimidine Nucleosides1 , 1959 .

[13]  R. Cline,et al.  Chromatography of Pyrimidine Reduction Products , 1956 .

[14]  G. Hilbert.  The Alkylation of Pyrimidines. An Attempt to Prepare 1-Glucosidocytosine , 1934 .