1965
DOI: 10.1021/jm00325a038
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1-(2-Deoxy-D-glucopyranosyl)-5-fluorocytosine1

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1965
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Cited by 6 publications
(7 citation statements)
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“…In our current study, we decided to verify the performance of recently redesigned STO(1M)‐3G basis sets for prediction of nuclear shieldings and chemical shifts of an important antifungal drug and anticancer prodrug—5‐fluorocytosine (5FC) …”
Section: Introductionmentioning
confidence: 99%
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“…In our current study, we decided to verify the performance of recently redesigned STO(1M)‐3G basis sets for prediction of nuclear shieldings and chemical shifts of an important antifungal drug and anticancer prodrug—5‐fluorocytosine (5FC) …”
Section: Introductionmentioning
confidence: 99%
“…5FC belongs to the group of the fluorinated pyrimidine analogues. It was used for the first time in 1968 in the treatment of systemic fungal infections . Nowadays, it is widely used in combination with amphotericin B in the treatment of serious infections caused by Candida (septicemia and endocarditis) and Cryptococcus (meningitis and pulmonary infections) .…”
Section: Introductionmentioning
confidence: 99%
“…The product, 1.92 g. (96%), carefully protected from atmospheric moisture, was dried in vacua at 80°over P»06; ^ 1 2.93 (NH), 3.6-4.0 and 6.21 (Nils'9, 6.35 and 6.92 µ (CO, •, Anal. Cak'd, for Cu,H]3Cl2N3O2-0.25H2O: C, 51.7; H, 5.66; Cl.…”
mentioning
confidence: 99%
“…210-212°: [ ]29> +10°(1% in 1 HCI); %; 2.80, 2.95, and 3.1 (NH, NH. ), 3.05, 3.81, 6.12, and 6.50 (NH* %), 6.27 and 7.12 µ (CO*™). Experimental Mills Reaction with 2-Dimethylamino-5-aminopyridine.-2-Dimethylamino-5-nitropyridine6 was reduced in a Parr apparatus with 5% palladium on carbon in 95% ethanol.…”
mentioning
confidence: 99%
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