1988
DOI: 10.1002/chin.198813233
|View full text |Cite
|
Sign up to set email alerts
|

ChemInform Abstract: 5‐Fluorouracil Derivatives. Part 12. Synthesis and Antitumor Activity of α‐Alkylthiomethyl‐, α‐Alkylsulfinylmethyl‐, α‐Alkylsulfonylmethyl‐, and α‐Acylthiomethyl‐5‐fluorouracils.

Abstract: The 5‐fluorouracil derivatives (III) ‐ (V), (VIII), and (X) with sulfur‐containing side groups are prepared as outlined in the reaction scheme.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2019
2019
2019
2019

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 1 publication
0
1
0
Order By: Relevance
“…No further reaction was observed when sulfoxides 9-10 were treated with excess hydrogen peroxide. Heating with sodium periodate in water [31] resulted in a nonselective nucleobase oxidation. A similar result was achieved when the Oxone in methanol method [32] was employed.…”
Section: Chemistrymentioning
confidence: 99%
“…No further reaction was observed when sulfoxides 9-10 were treated with excess hydrogen peroxide. Heating with sodium periodate in water [31] resulted in a nonselective nucleobase oxidation. A similar result was achieved when the Oxone in methanol method [32] was employed.…”
Section: Chemistrymentioning
confidence: 99%