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- W2950295416 abstract "A new, safe, and efficient methodology for the thiocyanation of some aminopyrimidine derivatives has been implemented. The thiocyanation reactions proceeded at room temperature with high yields and selectivity. This route is a less toxic alternative to other common thiocyanation techniques because it uses molecular iodine as a halogen source, which is less reactive and easier to handle than chlorine or bromine." @default.
- W2950295416 created "2019-06-27" @default.
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- W2950295416 date "2011-08-11" @default.
- W2950295416 modified "2023-09-26" @default.
- W2950295416 title "ChemInform Abstract: Iodine Mediated an Efficient and Greener Thiocyanation of Aminopyrimidines by a Modification of the Kaufmann′s Reaction." @default.
- W2950295416 cites W2042848024 @default.
- W2950295416 doi "https://doi.org/10.1002/chin.201136163" @default.
- W2950295416 hasPublicationYear "2011" @default.
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