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N-Carbobenzoxy-L-proline

A soln. of N-trifluoroacetylimidazole in dry tetrahydrofuran added at 0° to a soln. of N-carbohenzoxy-L-proline and p-nitrophenol in the same solvent, kept an additional hr. at 0°, then stirred 4 hrs. at room temp. N-carbobenzoxy-L-proline p-nitrophenyl ester. Y 78.5%. — In general, the use of 1-acylimidazoles seems less satisfactory then available alternatives, but may be useful in some specific instances. F. e. s. H. D. Law, Soc. 1965, 3897. [Pg.65]


See other pages where N-Carbobenzoxy-L-proline is mentioned: [Pg.1116]    [Pg.1116]    [Pg.1620]    [Pg.2519]    [Pg.2519]    [Pg.1116]    [Pg.1620]    [Pg.1116]    [Pg.1116]    [Pg.1620]    [Pg.1116]    [Pg.1116]    [Pg.1620]    [Pg.2519]    [Pg.2519]    [Pg.1116]    [Pg.1620]    [Pg.1116]    [Pg.1116]    [Pg.1620]    [Pg.89]    [Pg.380]    [Pg.104]    [Pg.125]    [Pg.427]   


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Carbobenzoxy

Carbobenzoxy-L-proline

L Proline

N- -proline

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