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Chemical synthesis peptide ester complexes

Deprotonation of a pyridinylmethylenic proton of pyridine- and bipyridine-based pincer complexes can lead to dearomatization. The dearomatized complexes can then activate a chemical bond (H-Y, Y = H, OH, OR, NH2, NR2, C) by cooperation between the metal and the ligand, thereby regaining aromatization (Figure 1.1). The overall process does not involve a change in the metal s oxidation state [6-8]. In this chapter, we describe the novel, environmentally benign catalytic synthesis of esters, amides, and peptides that operate via this new metal-ligand cooperation based on aromatization-dearomatization processes. [Pg.2]


See other pages where Chemical synthesis peptide ester complexes is mentioned: [Pg.4]    [Pg.280]    [Pg.68]    [Pg.83]    [Pg.26]    [Pg.132]    [Pg.102]    [Pg.376]    [Pg.36]    [Pg.835]    [Pg.65]    [Pg.641]    [Pg.48]    [Pg.1336]    [Pg.834]    [Pg.906]    [Pg.87]    [Pg.226]    [Pg.74]    [Pg.641]    [Pg.148]    [Pg.654]    [Pg.157]   
See also in sourсe #XX -- [ Pg.324 , Pg.325 , Pg.326 , Pg.327 , Pg.328 , Pg.329 ]




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Chemical complexes

Chemical complexity

Chemical synthesis peptides

Ester complexes

Peptide chemical

Peptide complexation

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Peptides esters

Peptides peptide ester complexes

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