Zobrazeno 1 - 6
of 6
pro vyhledávání: '"S R, Nicholls"'
Publikováno v:
Antiviral Chemistry and Chemotherapy. 5:162-168
Novel haloalkyl phosphate derivatives of the anti-HIV nucleoside analogue AZT were prepared by phosphorochloridate chemistry. These materials were designed to act as labile membrane-soluble prodrugs of the bio-active free nucleotides. In vitro evalua
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 3:1207-1210
The 5′-bis(trichloroethyl) phosphate derivatives of several 3′-O-acyl thymidines were prepared from the thymidine phosphate. Even though the parent nucleosides are inactive as antiviral agents, the phosphates are selective inhibitors of the proli
Publikováno v:
Antiviral Chemistry and Chemotherapy. 1:355-360
The reaction of thymidine, AZT (Fig. 1, compound 1) and ddCyd (Fig. 1, compound 2) with bis(2,2,2-trichloroethyl) phosphorochloridate gave novel 5′-bis(2,2,2-trichloroethyl) phosphates, characterized by spectroscopic and analytical data. Analogous
Publikováno v:
Antiviral Chemistry and Chemotherapy. 1:25-33
The reaction of thymidine with diethyl, dipropyl, and dibutyl phosphorochloridates yields novel 5′-(dialkyl phosphates), characterized by spectroscopic and analytical data. These are readily mesylated at the 3′-position. Similar reaction of 3′-
Publikováno v:
AIDS (London, England). 4(4)
Autor:
D. Kinchington, Caleb Nickson, S. R. Nicholls, Christopher McGuigan, M.F. Wang, S. Galpin, T. J. O'Connor, D.J. Jeffries
Publikováno v:
Antiviral Research. 20:55