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Enantioselective Conjugate Arylation of Coumarins

Conjugate Arylation of Chiral, Racemic o,p-Unsaturated Carbonyl Compounds [Pg.290]

Conjugate Asymmetric Arylation of 3-Substituted a,P-unsaturated Carbonyl Compounds [Pg.291]

6- Addition of Arylboronic Adds to a,p,y,5-Unsaturated Carbonyl Compounds [Pg.291]

Recent approaches by Hayashi and others aimed at expanding the arylation chemistry to include also a,p,y,5-unsaturated carbonyl compounds as acceptors. In this vein, enynones such as 126 undergo a rhodium-Segphos (50)-catalyzed [Pg.291]

In a recent report by Csiky, 2,4-dienoate esters 130 were employed as electro-phihc partners for a rhodium] I)-catalyzed regioselective 1,6-addition of arylboronic [Pg.292]


See other pages where Enantioselective Conjugate Arylation of Coumarins is mentioned: [Pg.290]   


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Conjugate arylation

Conjugated enantioselectivity

Coumarin 2- arylation

Coumarins 2-arylation

Enantioselective arylation

Enantioselectivity conjugation

Of coumarin

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