Dephosphonylation of protected deoxynucleoside and oligodeoxynucleotide H-phosphonates
CB Reese, C Visintin
Index: Reese, Colin B.; Visintin, Cristina Tetrahedron Letters, 1999 , vol. 40, # 35 p. 6477 - 6480
Full Text: HTML
Citation Number: 4
Abstract
The conversion of four 5′-O-(4, 4′-dimethoxytrityl)-2′-deoxyribonucleoside 3′-H- phosphonates 1 (B= 4, 5, 6 and 7) into their partially-protected nucleoside precursors 3 (B= 4, 5, 6 and 7, respectively) in good isolated yields is described. The procedure used is also suitable for the dephosphonylation of protected oligonucleotide H-phosphonate blocks.
Related Articles:
[Charubala, R.; Uhlmann, E.; Beiter, A. H.; Pfleiderer, W. Synthesis, 1984 , # 11 p. 965 - 968]
[Journal of the American Chemical Society, , vol. 104, # 5 p. 1316 - 1319]
[Journal of the American Chemical Society, , vol. 104, # 5 p. 1316 - 1319]
[Journal of the American Chemical Society, , vol. 104, # 5 p. 1316 - 1319]
[Helvetica Chimica Acta, , vol. 65, # 8 p. 2372 - 2393]