THE FLUORIDE-INDUCED REACTION OF PHENYLTHIO-, METHYLTHIO- AND METHOXY-SUBSTITUTED SILYLMETHYLAZOLES WITH CARBONYL COMPOUNDS

DOI: 10.1016/0040-4020(89)80092-4

Source and publish data:

Tetrahedron p. 637 - 642 (1989)

Update date:2022-08-05

Topics:

Authors:

Shimizu, Sumio

Ogata, Masaru

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Article abstract of DOI:10.1016/0040-4020(89)80092-4

Phenylthio-, methylthio- and methoxy-substituted silylmethylazoles, which act as substituted (N-azolyl)methylanion equivalents, were prepared and made to react with carbonyl compounds in the presence of fluoride anion to obtain 2-phenylthio-, 2-methylthio

Full text of DOI:10.1016/0040-4020(89)80092-4

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