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Carbonyl recognition

S. Saito, H. Yamamoto, Carbonyl Recognition, in Modern Carbonyl Chemistry (J. Otera, Ed.), Wiley-VCH, Weinheim, 2000, 33-67. [Pg.455]

Astonishing behavior of ATPH in a carbonyl recognition event was highlighted in the kinetic generation of more substituted enolates of unsymmetrical dialkyl ketones [28]. Most likely, ATPH prefers coordination with one of the lone pairs of carbonyl oxygen anti to the more sterically hindered a-carbon of unsymmetrical... [Pg.42]

By carbonyl recognition by complexation with specialized aluminum reagents... [Pg.213]

See other pages where Carbonyl recognition is mentioned: [Pg.34]    [Pg.34]    [Pg.35]    [Pg.37]    [Pg.39]    [Pg.41]    [Pg.43]    [Pg.45]    [Pg.47]    [Pg.49]    [Pg.51]    [Pg.53]    [Pg.55]    [Pg.57]    [Pg.59]    [Pg.61]    [Pg.63]    [Pg.63]    [Pg.64]    [Pg.65]    [Pg.67]    [Pg.244]    [Pg.639]   
See also in sourсe #XX -- [ Pg.33 ]



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Recognition of Carbonyl Substrate with Bulky Lewis Acid

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