FORMATION OF 2-PHENYL-γ-BENZPYRONE (FLAVONE) IN NUCLEOPHILIC THIYLATION OF 1-(2'-HYDROXYPHENYL)-3-PHENYLPROP-1-YN-ONE BY POTASSIUM p-THIOCRESOLATE

DOI: 10.1007/BF00519524

Source and publish data:

Chemistry of Heterocyclic Compounds p. 490 - 491 (1986)

Update date:2022-08-04

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Authors:

Korshunov, S. P.

Statsyuk, V. E.

Kazantseva, V. M.

Bodrikov, I. V.

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Article abstract of DOI:10.1007/BF00519524

The mechanism of formation of 2-phenyl-γ-benzpyrone (flavone) in nucleophilic thiylation of 1-(2'-hydroxyphenyl)-3-phenylprop-2-yn-1-one by potassium p-thiocresolate has been established by IR and PMR spectroscopy.

Full text of DOI:10.1007/BF00519524

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