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Enantioselective nickel-catalysed conjugate addition reactions

Enantioselective Nickel(ii)-Catalysed Conjugate Addition Reactions... [Pg.36]

The second chapter of the book covered the advances in enantioselective nickel(ii)-catalysed conjugate additions. An important breakthrough in the history of the Michael reaction was the achievement of the Michael addition of p-dicarbonyl compounds to a broad variety of electrophiles catalysed by nickel acetylacetonate, described by Nelson in 1979-1980. Since this pioneering contribution, nickel has become one of the preferred metals in catalytic Michael reactions. Later, in 1988, Soai developed the first asymmetric conjugate additions performed under chiral nickel(ii) catalysis. Ever since. [Pg.345]


See other pages where Enantioselective nickel-catalysed conjugate addition reactions is mentioned: [Pg.39]    [Pg.49]    [Pg.61]    [Pg.77]    [Pg.96]    [Pg.221]    [Pg.322]    [Pg.46]    [Pg.65]    [Pg.346]    [Pg.56]    [Pg.65]    [Pg.129]    [Pg.74]    [Pg.37]    [Pg.41]    [Pg.60]   


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Addition, conjugate enantioselectivity

Catalysed reactions

Conjugate addition enantioselective

Conjugate addition nickel catalysed

Conjugate addition reactions

Conjugate addition reactions enantioselective

Conjugate reaction

Conjugated addition reaction

Conjugated enantioselectivity

Conjugated reaction

Conjugative reactions

Enantioselective additions

Enantioselective reaction

Enantioselectivity addition reactions

Enantioselectivity conjugation

Nickel addition

Nickel addition reactions

Nickel-catalysed reactions

Reaction nickel

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