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Allyl protecting groups, cleavage, tetrakis palladium

Allyl protection of terminal a-carboxy groups has been used in convergent syntheses of N-linked glycopeptides on a solid support.PI For instance, the polymer-bound trisaccharide pentapeptide allyl ester 12 (Scheme 7) is built up by condensation of the polymer-linked trisaccharide with Z-Ala-Ile-Asp-Ile-Ser(Bzl)-OAl. Further conversion into the polymer-bound trisaccharide octapeptide derivative 14 is achieved by cleavage of the allyl ester with tetrakis(triphenylphosphine)palladium and A,A-dimethylbarbituric acid to give 13, followed by condensation with H-Asp(OMob)-Leu-Thr(Bzl)-OAl. The presence of the allyl ester group at the C-terminus of the octapeptide provides the opportunity for further chain elongation. [Pg.761]


See other pages where Allyl protecting groups, cleavage, tetrakis palladium is mentioned: [Pg.88]    [Pg.252]    [Pg.345]    [Pg.376]    [Pg.342]    [Pg.206]    [Pg.295]    [Pg.74]   
See also in sourсe #XX -- [ Pg.471 , Pg.472 ]




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Allyl cleavage

Allyl group

Allyl group cleavage

Allyl protecting groups, tetrakis

Allyl protecting groups, tetrakis palladium

Allylic cleavage

Allyls palladium

Cleavage allyl groups, tetrakis palladium

Palladium allylation

Palladium groups

Protecting group, allyl

Tetrakis palladium

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