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- W2065437034 abstract "An attempt was made to prepare 2-benzylquinoxalin-3-one by hydrolyzing the azlactone, 2-phenyl-4-benzylidene-5-oxazolone to β-phenylpyruvic acid and then treating this in situ with o-phenylenediamine (OPDA). The initial hydrolysis apparantly proceeded only as far as opening the azlactone ring forming 2-benzamidocinnamic acid which condensed with OPDA to form a substituted styrylbenzimidazole." @default.
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- W2065437034 date "1970-12-01" @default.
- W2065437034 modified "2023-09-24" @default.
- W2065437034 title "A new route to 2-styrylbenzimidazoles" @default.
- W2065437034 cites W2154037394 @default.
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- W2065437034 doi "https://doi.org/10.1002/jhet.5570070624" @default.
- W2065437034 hasPublicationYear "1970" @default.
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