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Acrylic acid , reaction with carbon-centered

Based on extensive studies of C-H transformation with Pd(ii), Yu et al. recently achieved asymmetric desymmetrization in a CDC reaction (Scheme 7.26). ° Boc-L-Isoleucine (Boc-Ile-OH) was an effective chiral ligand for the Pd(ii)-catalyzed enantioselective C-H activation of a,a-diphenylacetic acid Na salt. The resultant Pd-aryl intermediate is considered to undergo insertion into styrenes or acrylates, followed by p-hydrogen elimination to afford the coupling product with a chiral quaternary carbon center in good... [Pg.149]


See other pages where Acrylic acid , reaction with carbon-centered is mentioned: [Pg.591]    [Pg.237]    [Pg.159]    [Pg.112]    [Pg.21]    [Pg.148]    [Pg.645]    [Pg.2013]    [Pg.218]    [Pg.182]    [Pg.359]    [Pg.102]    [Pg.333]    [Pg.788]    [Pg.969]    [Pg.365]    [Pg.155]    [Pg.191]    [Pg.595]   


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Acid centers

Acrylate reaction

Acrylic acid carbonates

Acrylic acid reaction

Carbon centers

Carbon-centered

Carbonate reactions with

Reaction center

Reaction with acrylic acid

Reaction with carbon

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