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Br0nsted acid chiral

As a stronger Br0nsted acid, chiral binaphthol-based phosphoric acid 8 and /V-triflyl phosphoramide 9 were recently introduced to the FCA reaction of enones. Reports by a few groups on the alkylations of indoles showed that simple enones were still challenging substrates, and modest ee values were recorded with a few examples over 90% ee (Scheme 9.8) [23]. However, excellent enantioselectivities were achieved in the intramolecular C3 and N1 alkylations of indole by You and co-workers (Scheme 9.9) [24]. Noteworthy, chiral oxazaborolidinone and... [Pg.317]

Br0nsted Acid/Chiral (Thio)urea Combination... [Pg.173]

Br0nsted Acids Chiral Phosphoric Acid Catalysts in Asymmetric Synthesis... [Pg.289]

Br0nsted Acids Chiral (Thio)urea Derivatives... [Pg.315]


See other pages where Br0nsted acid chiral is mentioned: [Pg.461]    [Pg.575]   
See also in sourсe #XX -- [ Pg.322 , Pg.323 , Pg.324 , Pg.325 , Pg.333 , Pg.337 ]




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Br0nsted

Br0nsted acid

Br0nsted acidity

Br0nsted acids strong chiral

Chiral Br0nsted acid catalysis

Chiral acids

Metal-free reduction of imines enantioselective Br0nsted acid-catalyzed transfer hydrogenation using chiral BINOL-phosphates as catalysts

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