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- W2075336593 startingPage "389" @default.
- W2075336593 abstract "The reactions of 1-unsubstituted and 1-methyl-2-(o-methylthiophenyl)vinyl bromides in acetic acid in the presence of silver salt gave exclusively benzothiophenes, while the corresponding 2-methoxyphenyl analogues were unreactive under similar conditions. This cyclization is considered to involve an intramolecular nucleophilic attack of the sulfur atom at the carbon atom of the double bond activated by the silver ion with the elimination of the silver bromide." @default.
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- W2075336593 date "1976-04-05" @default.
- W2075336593 modified "2023-10-18" @default.
- W2075336593 title "SILVER ION-ASSISTED INTRAMOLECULAR NUCLEOPHILIC ADDITION-ELIMINATION OF VINYL BROMIDES; FORMATION OF BENZOTHIOPHENES FROM 2-(o-METHYLTHIOPHENYL)VINYL BROMIDES" @default.
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- W2075336593 doi "https://doi.org/10.1246/cl.1976.389" @default.
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