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Catalytic system adamantyl

Aryl coupling reactions. A highly active catalytic system for Suzuki coupling contains Pd(OAc)2, KF, and di-/-butyl-2-biphenylphosphine. but the most efficient catalyst to date is the combination of Pd(OAc)2 and bis(l-adamantyl)butylphosphine, which is effective to couple deactivated AiCl on very low Pd loading (down to 0.001 mol%) yet showing turnover number in the 10,(X)0-20,(XX) range. Products are obtained in good yields. [Pg.321]

Ackermaim showed in 2005 that phosphine oxide R2P(0)H additives efficiently activate the ruthenium(ll) catalyst, which allowed the direct C-H bond arylation with the less reactive but readily available arylchlorides, such as (adamantyl)2-P(0)H (Ad2P(0)H) associated with [RuCl2(p-cymene)]2 (Scheme 2) [44]. This catalytic system was used for the monoarylation with arylchlorides of ketimines to... [Pg.123]


See other pages where Catalytic system adamantyl is mentioned: [Pg.354]    [Pg.737]    [Pg.158]    [Pg.508]    [Pg.676]    [Pg.72]    [Pg.59]    [Pg.522]    [Pg.357]    [Pg.364]    [Pg.227]    [Pg.529]    [Pg.501]    [Pg.468]    [Pg.120]    [Pg.2069]    [Pg.114]    [Pg.202]    [Pg.117]   
See also in sourсe #XX -- [ Pg.198 ]




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Catalytic system

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