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Hydrogen bonding amides, secondary

Proline is the only amino acid in Table 27.1 that is a secondary amine, and its presence in a peptide chain introduces an amide nitrogen that has no hydrogen available for hydrogen bonding. This disrupts the network of hydrogen bonds and divides the peptide into two separate regions of a helix. The presence of proline is often associated with a bend in the peptide chain. [Pg.1144]

N-hydroxylation is not restricted to primary and secondary amines. For example, nitrogen-based functional groups such as amides, amidino, guanidino, hydrazino, etc. that have at least one nitrogen-hydrogen bond are susceptible to N-hydroxylation. [Pg.98]


See other pages where Hydrogen bonding amides, secondary is mentioned: [Pg.95]    [Pg.741]    [Pg.15]    [Pg.262]    [Pg.317]    [Pg.8]    [Pg.342]    [Pg.192]    [Pg.98]    [Pg.6828]    [Pg.338]    [Pg.130]    [Pg.1515]    [Pg.1144]    [Pg.1144]    [Pg.1144]    [Pg.205]    [Pg.183]    [Pg.1144]    [Pg.1144]    [Pg.162]    [Pg.412]    [Pg.677]    [Pg.1038]    [Pg.2]    [Pg.79]    [Pg.106]    [Pg.258]    [Pg.32]    [Pg.950]    [Pg.194]    [Pg.274]    [Pg.136]    [Pg.354]    [Pg.473]    [Pg.31]    [Pg.310]    [Pg.643]    [Pg.302]    [Pg.311]    [Pg.29]    [Pg.31]    [Pg.58]    [Pg.47]    [Pg.270]    [Pg.43]    [Pg.62]    [Pg.311]   
See also in sourсe #XX -- [ Pg.108 ]




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Amide bonds

Amide hydrogen bonds

Amides hydrogenation

Amides: , bonding

Amidic hydrogen bonding

Hydrogen bonding amides

Secondary amide

Secondary bonding

Secondary bonds

Secondary hydrogen

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