Synthesis and biological evaluation of new bicyclic fluorinated uracils through ring-closing metathesis.
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[1] S. Fustero,et al. A versatile synthesis of fluorinated uracils in solution and on solid-phase. , 2004, Organic letters.
[2] L. Kotra,et al. Structure-activity relationships of 2'-deoxy-2',2'-difluoro-L-erythro-pentofuranosyl nucleosides. , 1997, Journal of medicinal chemistry.
[3] I. Ojima,et al. Biomedical Frontiers of Fluorine Chemistry , 1996 .
[4] M. Villarroya,et al. Palladium(0)-catalysed allylation of uracils and thiouracils. Influence of the solvent on the regioselectivity of the allylation , 1996 .
[5] S. Ozaki. Synthesis and antitumor activity of 5‐fluorouracil derivatives , 1996, Medicinal research reviews.
[6] M. Villarroya,et al. Palladium-catalyzed allylation of pyrimidine-2,4-diones (uracils) and of 6-membered heterocyclic ambident sulfur nucleophiles , 1993 .
[7] L. Hertel,et al. Synthesis of 2-deoxy-2,2-difluoro-D-ribose and 2-deoxy-2,2'-difluoro-D-ribofuranosyl nucleosides , 1988 .
[8] R. W. Lang,et al. Fluorine-containing organozinc reagents. V.: The reformatskii-claisen reaction of chlorodifluoroacetic acid derivatives , 1988 .