Synthesis and reactions of 2',3'-anhydro-1-β-d-ribofuranosyl-uracil derivatives: molecular structures of 3-methyl-2',3'-anhydrouridine and 3,5-dimethyl-2',3':O6,5'-dianhydrouridine

[1]  D. Clark,et al.  Studies on the interconversion of 2,3'-anhydro-1-β-D-xylofuranosyluracil and 2,2'-anhydro-1-β-D-arabinofuranosyluracil , 1979 .

[2]  D. Cremer,et al.  General definition of ring puckering coordinates , 1975 .

[3]  G. Horváth,et al.  Bromination of 2,2′-anhydrouridine , 1975 .

[4]  E. Lovett,et al.  Mass spectroscopy of pyrimidine cyclonucleosides. , 1973, Journal of the American Chemical Society.

[5]  D. Lipkin,et al.  The iodination of thymidine. A synthesis of O 6 ,5'-cyclothymidine. , 1971, Journal of the American Chemical Society.

[6]  J. Fox,et al.  Nucleosides. LXV. Synthesis and reactions of some pyrimidine 2',6-anhydronucleosides. , 1970, The Journal of organic chemistry.

[7]  L. Orgel,et al.  Studies in prebiotic synthesis. V. Synthesis and photoanomerization of pyrimidine nucleosides. , 1970, Journal of molecular biology.

[8]  J. Fox,et al.  Nucleosides. 58. Transformations of pyrimidine nucleosides in alkaline media. 3. The conversion of 5-halogenouridines into imidazoline and barbituric acid nucleosides. , 1969, The Journal of organic chemistry.

[9]  K. Kikugawa,et al.  Reactions of Methyl Iodide on 2, 2'-Anhydro-1-(β-D-arabinofuranosyl)-uracil and 2, 3'-Anhydro-1-(β-D-xylofuranosyl) uracil , 1969 .

[10]  J. Fox,et al.  Nucleosides. LII. Transformations of pyrimidine nucleosides in alkaline media. I. The conversion of 5-halogenoarabinosyluracils into imidazoline nucleosides. , 1968, The Journal of organic chemistry.

[11]  James B. Hendrickson,et al.  Molecular geometry. VII. Modes of interconversion in the medium rings , 1967 .

[12]  J. Fox,et al.  Nucleosides. XXXIX. 2'-deoxy-2'-fluorocytidine, 1-beta-D-arabinofuranosyl-2-amino-1,4(2H)-4-iminopyrimidine, and related derivatives. , 1967, The Journal of organic chemistry.

[13]  P. K. Chang.  Iodination of 2'-deoxycytidine and related substances. A reinvestigation of the structures of the by-product, C9H10I2N2O5, and its derivatives. , 1965, The Journal of organic chemistry.

[14]  M. Hirata,et al.  The nucleophilic substitution of secondary sulfonyloxy groups of pyrimidine nucleosides. , 1965, Chemical & pharmaceutical bulletin.

[15]  J. F. Codington,et al.  Nucleosides. XIX. Structure of the 2'-Halogeno-2'-Deoxypyrimidine Nucleosides1 , 1964 .

[16]  J. F. Codington,et al.  Nucleosides. XVIII. Synthesis of 2'-Fluorothymidine, 2'-Fluorodeoxyuridine, and Other 2'-Halogeno-2'-Deoxy Nucleosides1,2 , 1964 .

[17]  J. Fox,et al.  Nucleosides. X. Anhydronucleosides and Related Compounds Derived from 2',5'-Di-O-trityluridine1-3 , 1961 .