A UNIQUE TRIMOLECULAR MICHAEL REACTION AND CYCLIZATION

DOI: 10.1016/S0040-4020(01)89531-4

Source and publish data:

Tetrahedron p. 6545 - 6552 (1989)

Update date:2022-09-26

Topics:

Authors:

Al-Arab, Mohamed M.

Ghanem, Bader S.

Fitton, Alan O.

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Article abstract of DOI:10.1016/S0040-4020(01)89531-4

1,3-Diaryl-2-propene-1-ones react with ethyl cyanoacetate in presence of sodium ethoxide at room temperature to give 2-aroyl-1,3,5-triaryl-4-carbethoxy-4-cyanocyclohexanols.The structure of the reaction products was established by infrared, H-1 and C-13 n

Full text of DOI:10.1016/S0040-4020(01)89531-4

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Product name:2-(4-bromobenzoyl)-1-(4-bromophenyl)-4-carboethoxy-4-cyano-3,5-di-(4-tolyl) cyclohexanol

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