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Bronsted acid-surfactant combined

Shekouhy, M. (2012). Sulfuric acid-modified PEG-6000 (PEG-OS03H) an efficient Bronsted acid-surfactant combined catalyst for the one-pot three component synthesis of a-aminonitriles in water. [Pg.77]

Manabe, K. and Kobayashi, S., Mannich-type reactions of aldehydes, amines, and ketones in a colloidal dispersion system created by a Bronsted acid-surfactant-combined catalyst in water, Org. Lett., 1999, 1, 1965-1967. [Pg.254]

Sc(() l f) ( is an effective catalyst of the Mukaiyama aldol reaction in both aqueous and non-aqueous media (vide supra). Kobayashi et al. have reported that aqueous aldehydes as well as conventional aliphatic and aromatic aldehydes are directly and efficiently converted into aldols by the scandium catalyst [69]. In the presence of a surfactant, for example sodium dodecylsulfate (SDS) or Triton X-100, the Sc(OTf)3-catalyzed aldol reactions of SEE, KSA, and ketene silyl thioacetals can be performed successfully in water wifhout using any organic solvent (Sclieme 10.23) [72]. They also designed and prepared a new type of Lewis acid catalyst, scandium trisdodecylsulfate (STDS), for use instead of bofh Sc(OTf) and SDS [73]. The Lewis acid-surfactant combined catalyst (LASC) forms stable dispersion systems wifh organic substrates in water and accelerates fhe aldol reactions much more effectively in water fhan in organic solvents. Addition of a Bronsted acid such as HCl to fhe STDS-catalyzed system dramatically increases the reaction rate [74]. [Pg.424]


See other pages where Bronsted acid-surfactant combined is mentioned: [Pg.153]    [Pg.322]    [Pg.134]    [Pg.303]    [Pg.180]    [Pg.245]    [Pg.153]    [Pg.322]    [Pg.134]    [Pg.303]    [Pg.180]    [Pg.245]    [Pg.185]    [Pg.698]    [Pg.185]    [Pg.478]   


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