- a
range of
addition reactions; with
aliphatic imidates generally reacting faster than
aromatic imidates. They can be
hydrolyzed to give
esters and by...
- 1002/cber.18830160235. Roger, R.; Neilson, D. G. (1961). "The
Chemistry of
Imidates". Chem. Rev. 61 (2): 179–211. doi:10.1021/cr60210a003. Adams, Roger; Thal...
-
Amine Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo
Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite...
-
Amine Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo
Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite...
-
Amine Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo
Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite...
-
Amine Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo
Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite...
- of glycosides.
Typical leaving groups are halides,
thioalkyl groups, or
imidates, but acetate, phosphate, and O-pentenyl
groups are also emplo****. Natural...
-
Amine Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo
Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite...
-
Amine Enamine Ammonium Hydrazo Nitrene Imine Oxime Hydrazone Azo
Amide Imidate Amidine Carbamate Imide Nitrile Isonitrile Cyanate Isocyanate Nitrate Nitrite...
-
presented below. The (1,5) or (3,4) bond can be
formed by the
reaction of an
imidate and an α-aminoaldehyde or α-aminoacetal. The
example below applies to imidazole...
