CONJUGATE ADDITION OF GRIGNARD REAGENTS TO UNSATURATED KETONES: GC/MS-HPLC STUDY. ISOLATION AND OXIDATION OF E AND Z ENOLS OF A KETONE

DOI: 10.1016/S0040-4020(01)86206-2

Source and publish data:

Tetrahedron p. 6801 - 6806 (1988)

Update date:2022-08-02

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Authors:

Pinkus, A. G.

Logaraj, S.

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Article abstract of DOI:10.1016/S0040-4020(01)86206-2

The conjugate addition of phenylmagnesium bromide to benzalacetomesitylene (1) was studied.The only product resulting from 1,4-addition was Kohler's ketone (4) in 84+/-1 percent yield based on (1) by isolation and analysis.The byproducts from 4 were forme

Full text of DOI:10.1016/S0040-4020(01)86206-2

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