Palladium-catalyzed coupling reactions of uracil nucleosides and nucleotides
CF Bigge, P Kalaritis, JR Deck…
Index: Bigge,C.F.; Kalaritis,P.; Deck,J.R. Journal of the American Chemical Society, 1980 , vol. 102, p. 2033
Full Text: HTML
Citation Number: 61
Abstract
Abstract: A new method is described for the facile alkylation of uracil nucleotides. Treatment of the unprotected nucleotide with mercuric acetate followed by the addition of styrene or ring-substituted styrenes and lithium tetrachloropalladate affords the C-5-trans-styryl derivatives. The coupling reactions using nucleosides or nucleotides proceed in moderate to good yield, can be run in protic solvents, are not adversely affected by the presence of the ...
Related Articles:
[Anderson, Aaron S.; Hwang, Jae-Taeg; Greenberg, Marc M. Journal of Organic Chemistry, 2000 , vol. 65, # 15 p. 4648 - 4654]
[Anderson, Aaron S.; Hwang, Jae-Taeg; Greenberg, Marc M. Journal of Organic Chemistry, 2000 , vol. 65, # 15 p. 4648 - 4654]
[Anderson, Aaron S.; Hwang, Jae-Taeg; Greenberg, Marc M. Journal of Organic Chemistry, 2000 , vol. 65, # 15 p. 4648 - 4654]
[Anderson, Aaron S.; Hwang, Jae-Taeg; Greenberg, Marc M. Journal of Organic Chemistry, 2000 , vol. 65, # 15 p. 4648 - 4654]
[Anderson, Aaron S.; Hwang, Jae-Taeg; Greenberg, Marc M. Journal of Organic Chemistry, 2000 , vol. 65, # 15 p. 4648 - 4654]