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Direct Suzuki-Miyaura type reaction

Directed orf/to-metalation (DoM) chemistry [81] further reinforces the versatility of nickel-catalyzed C-O bond activation reactions. Based on the strong accelerating and orf/to-directing effect of carbamate functionality in the base-induced deprotonation of arenes, an array of electrophiles can be introduced at the ortho position of aryl carbamates. For instance, DoM of dicarbamate, followed by 1,2-addition to a,(3-unsaturated aldehyde and intramolecular cyclization, furnishes the 2//-chromene derivative (Scheme 8) [82]. The carbamate director can finally be arylated under a nickel-catalyzed Suzuki-Miyaura-type reaction [47]. [Pg.51]


See other pages where Direct Suzuki-Miyaura type reaction is mentioned: [Pg.141]    [Pg.141]    [Pg.46]    [Pg.48]    [Pg.2]    [Pg.26]    [Pg.653]    [Pg.794]    [Pg.204]    [Pg.16]    [Pg.2]   
See also in sourсe #XX -- [ Pg.141 ]




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Direct reactions

Directed reactions

Miyaura

Miyaura reaction

Reaction direct reactions

Reaction direction

Suzuki reaction

Suzuki reaction reactions

Suzuki-Miyaura reaction

Suzuki-Miyaura-type

Suzuki-type

Suzuki-type reaction

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