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Esterification Yamada reactions

The procedure described is essentially that of Shioiri and Yamada. Diphenyl phosphorazidate is a useful and versatile reagent in organic synthesis. It has been used for racemlzatlon-free peptide syntheses, thiol ester synthesis, a modified Curtius reaction, an esterification of a-substituted carboxylic acld, formation of diketoplperazines, alkyl azide synthesis, phosphorylation of alcohols and amines,and polymerization of amino acids and peptides. - Furthermore, diphenyl phosphorazidate acts as a nitrene source and as a 1,3-dipole.An example in the ring contraction of cyclic ketones to form cycloalkanecarboxylic acids is presented in the next procedure, this volume. [Pg.188]

Yamada, T. (1996) Effect of reaction variables on TPA-EG continuous esterification with recycling in PET production process. Polym. React Eng., 4 (1), 1—45. [Pg.108]


See other pages where Esterification Yamada reactions is mentioned: [Pg.140]    [Pg.110]    [Pg.129]    [Pg.132]    [Pg.138]   
See also in sourсe #XX -- [ Pg.501 ]




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