Conformationally locked carbocyclic nucleosides built on abicyclo[3.1.0]hexane template with a fixed Southern conformation.Synthesis and antiviral activity
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[1] R. Wagner,et al. Nucleosides with a twist. Can fixed forms of sugar ring pucker influence biological activity in nucleosides and oligonucleotides , 1996 .
[2] C. George,et al. Synthesis, Conformational Analysis, and Biological Activity of a Rigid Carbocyclic Analogue of 2′-Deoxy Aristeromycin Built on a Bicyclo[3.1.0]hexane Template # , 1996 .
[3] K. Altmann,et al. 1′,6′-methano carbocyclic thymidine: Synthesis, x-ray crystal structure, and effect on nucleic acid duplex stability , 1994 .
[4] K. Altmann,et al. 4′,6′-Methano carbocyclic thymidine: A conformationally constrained building block for oligonucleotides , 1994 .
[5] P. Wyatt,et al. Synthesis and antiviral activity of 9-alkoxypurines. 1. 9-(3-Hydroxypropoxy)- and 9-[3-hydroxy-2-(hydroxymethyl)propoxy]purines , 1990 .
[6] R. Okazaki,et al. An Ab Initio Molecular Orbital Study on the Conformations of Bicyclo[3.1.0]hexane Derivatives , 1988 .
[7] Y. Shealy,et al. Synthesis of the carbocyclic analogs of uracil nucleosides , 1976 .
[8] M. Sundaralingam,et al. Conformational analysis of the sugar ring in nucleosides and nucleotides. A new description using the concept of pseudorotation. , 1972, Journal of the American Chemical Society.
[9] K. Ninomiya,et al. Diphenylphosphoryl azide. A new convenient reagent for a modified Curtus reaction and for the peptide synthesis. , 1972, Journal of the American Chemical Society.