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- Compelling evidence for a stepwise mechanism of the alkaline cyclisation of uridine 3′-phosphate esters. Harri Lönnberg, Roger Strömberg, Andrew Williams
, Org. Biomol. Chem.
, 2004
, 2
, 2165
- Linear free energy relationships in RNA transesterification: theoretical models to aid experimental interpretations. Ming Huang, Darrin M. York
, Phys. Chem. Chem. Phys.
, 2014
, 16
, 15846
- Intracomplex general acid/base catalyzed cleavage of RNA phosphodiester bonds: the leaving group effect. Tuomas Lönnberg, Mikko Luomala
, Org. Biomol. Chem.
, 2012
, 10
, 6785
- 138. The constitution of yeast ribonucleic acid. Part IV. Syntheses of uridylic and guanylic acids, uridine-5-phosphate and guanosine-5-phosphate. J. Masson Gulland, G. Ivan Hobday
, J. Chem. Soc.
, 1940
, 746
- General base catalysis vs. medium effects in the hydrolysis of an RNA model. Anthony J. Kirby, Robert E. Marriott
, J. Chem. Soc., Perkin Trans. 2
, 2002
, 422
- Di-uridine 3′-phosphate. Bernard Rayner, Colin B. Reese, Aiko Ubasawa
, J. Chem. Soc., Chem. Commun.
, 1980
, 972
- The mechanism of the metal ion promoted cleavage of RNA phosphodiester bonds involves a general acid catalysis by the metal aquo ion on the departure of the leaving group. Satu Mikkola, Eeva Stenman, Kirsi Nurmi, Esmail Yousefi-Salakdeh, Roger Strömberg, Harri Lönnberg
, J. Chem. Soc., Perkin Trans. 2
, 1999
, 1619
- The analysis of enzymic free energy relationships using kinetic and computational models. Ian R. Greig
, Chem. Soc. Rev.
, 2010
, 39
, 2272
- Cyanamide as a prebiotic phosphate activating agent – catalysis by simple 2-oxoacid salts. Maria Tsanakopoulou, John D. Sutherland
, Chem. Commun.
, 2017
, 53
, 11893
- 34. The nature of the phosphorus compounds present in cells of Bact. lactis aerogenes. P. C. Caldwell
, J. Chem. Soc.
, 1951
, 166