Synthesis and biological activities of 2-Pyrimidinone Nucleosides. III.^1,2 5-Alkynyl-2-Pyrimidinone 2′-Deoxyribosides

References

• Schroeder , A. C . 1981 . J. Med. Chem. , 24 : 109 (Paper I. of this series)
   PubMed Web of Science ®Google Scholar
• Efange , S. , Alessi , E. M. and Shih , H. C . 1985 . J. Med. Chem. , 28 : 904 (Paper II of this series)
   PubMed Web of Science ®Google Scholar
• Laland , S. G. and Serk-Hannsen , G. 1964 . Biochem. J. , 90 : 76
   PubMedGoogle Scholar
• De Clerq , E and Balzarini , J . 1983 . J. Med. Chem. , 26 : 661
   Google Scholar
• Robins , M. J. and Barr , P. J. 1983 . J. Org. Chem. , 48 : 1854
   Web of Science ®Google Scholar
• Vincent , P. and Beaucourt , J.-P . 1981 . Tetrahedron Lett. , 22 : 945
   Google Scholar
• Arantz , B. W and Brown , D. J. 1971 . J. Chem. Soc. (C) , : 1889
   Google Scholar
• Fox , J. J. , Yung , N. C and Hoffer , M. J. 1961 . Amer. Chem. Soc. , 83 : 4066 (b) Kotick, M.P.; Szantay, C.; Bardos, T.J. J. Org. Chem. 1969, 34, 3806.
   Web of Science ®Google Scholar
• Marquez , V. E. Personal communication
   Google Scholar
• Vorbrüggen , H. and Krolikiewicz , K . 1981 . Chem. Ber. , 114 : 1234
   Google Scholar
• Prystas , S. and Sorm , F. 1965 . Collect. Czech. Chem. Commun , 30 : 2960
   Google Scholar
• Venner , H. 1960 . J. Chem. Ber. , 93 : 137
   Google Scholar
• Davoll , J. and Lythgoe , B. J. 1949 . Chem. Soc. (London) , : 2526
   Google Scholar
• Allerton , R. and Overend , W. G. 1951 . J. Chem. Soc. , : 1483
   Google Scholar
• De Clerq , E . 1983 . Pure and Applied Chem. , 55 : 623
   Google Scholar
• Edo , K. , Sakamoto , T. and Yamanaka , H. 1978 . Chem. Pharm. Bull. , 26 : 3843
   Web of Science ®Google Scholar
• Robins , M. J. and Robins , R. K. 1965 . J. Amer. Chem. Soc. , 87 : 4934
   PubMed Web of Science ®Google Scholar
• Wittenberg , E . 1968 . Chem. Ber. , 101 : 1614
   Google Scholar
• Samek , Z. F. and Farkas , J. 1965 . Collect. Czech. Chem. Commun. , 30 : 2149
   Google Scholar
• Booth , H . 1966 . Tetrahedron , 22 : 615
   Web of Science ®Google Scholar
• Cheng , Y.-C. , Domin , B. , Sharma , R. A. and Bobek , M. 1976 . Antimicrob. Agents Chemother , 10 : 119
   PubMed Web of Science ®Google Scholar
• In some cases, when this instrument did not show the “characteristic'' stretching frequency for the C=C bond, the Nicolet Model 1180 was used which showed a weak signal in the 2150–2250 cm-1 region. All the major absorption peaks (i. e., the frequencies listed) were similar when compared on the two instruments.
   Google Scholar