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Methyl pheny, ketone

The principles of the method are very nicely illustrated by one of the first affinity labeling experiments, the reaction of /exs-i.-phenylalanine chloro-methyl ketone (TPCK) with chymotrypsin.1 TPCK resembles substrates like fexs-L-pheny 1 alanine methyl ester, but the chloromethyl ketone group of TPCK is an alkylating reagent. [Pg.150]

REGIOSELECTIVE MONOALKYLATION OF KETONES VIA THEIR MANGANESE ENOLATES 2-BENZYL-6-METHYLCYCLOHEXANONE FROM 2-METHYLCYCLOHEXANONE (Cyclohexanone, 2-methyl-6-(pheny I methyl)-)... [Pg.302]

See other pages where Methyl pheny, ketone is mentioned: [Pg.141]    [Pg.637]    [Pg.33]    [Pg.354]    [Pg.867]    [Pg.944]    [Pg.634]    [Pg.243]    [Pg.25]    [Pg.3364]    [Pg.619]    [Pg.3363]    [Pg.619]    [Pg.2182]   
See also in sourсe #XX -- [ Pg.1030 ]



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2- pheny] methyl

5- -3-pheny

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