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Conjugate additions Brpnsted base catalysts

With respect to the catalysts employed in conjugate additions, a big collection of efficient stable and environmentally friendly natural or newly designed chiral organocatalysts has already been developed. These catalysts are usually cheap to prepare and readily accessible in a range of quantities. They fall into four major classes Lewis bases, Lewis acids, Brpnsted bases, and Brpnsted acids [If]. The identification of the generic modes of activation of these catalysts has been crucial to the success of organocatalysis. [Pg.42]

Chiral ion pairs (B, Fig. 2.2) can be formed by deprotonation of the pronucleophile with a chiral Brpnsted base or employing an achiral base and a chiral phase-transfer catalyst. Chiral phase-transfer catalysis (PTC) [8] illustrates how ion pairing interactions can be used to carry out the enantioface discrimination in conjugate addition reactions. In both cases, the chiral cation is responsible for... [Pg.42]


See other pages where Conjugate additions Brpnsted base catalysts is mentioned: [Pg.89]    [Pg.147]    [Pg.345]    [Pg.157]    [Pg.6]    [Pg.493]    [Pg.1709]    [Pg.182]    [Pg.169]   
See also in sourсe #XX -- [ Pg.494 , Pg.495 , Pg.496 , Pg.497 ]




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