Why natural DNA is based on 2′ -deoxyribose, with 3′,5′ phosphodiester links

Pure and Applied Chemistry

Volumn 68, Issue 11, 1996, Pages 2037-2041

  Breslow, Ronald ^a   Sheppard, Terry L ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000712481     PISSN: 00334545     EISSN: None     Source Type: Journal    
DOI: 10.1351/pac199668112037     Document Type: Article

References (9)

1. E. Anslyn and R. Breslow, J. Amer. Chem. Soc. 111, 4473 (1989).
2. C. J. Rizzo, J. P. Dougherty, and R. Breslow, Tetrahedron Lett. 33, 4129 (1992).
3. J. P. Dougherty, C. J. Rizzo, and R. Breslow, J. Amer. Chem. Soc. 114, 6254 (1992).
4. J. Stubbe, Adv. Enzymol. Relat. Areas Mol Biol. 63, 349 (1990).
5. A. Eschenmoser and E. Loewenthal, Chem. Soc. Rev. 21, 1 (1992) report related studies using sugars other than ribose.
6. H. Hashimoto and C. Switzer, J. Amer. Chem. Soc. 114, 6255 (1992).
7. R. Jin, W. H. Chapman, Jr., A. R. Srinivasan, W. K. Olson, R. Breslow, and K. J. Breslauer, Proc. Natl. Acad. Sci. USA 90, 10568 (1993).
8. T. L. Sheppard, A. T. Rosenblatt, and R. Breslow, J. Org. Chem. 59, 7243 (1994).
9. K.-Y. Jung and C. Switzer, J. Amer. Chem. Soc. 116, 6059 (1994).