A mild and efficient methodology for the rearrangement of protected asparagine and protected glutamine is reported; good results are obtained with a wide selection of protecting groups.
G. Angelici, S. Contaldi, S. L. Green, C. Tomasini (2008). Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement. ORGANIC & BIOMOLECULAR CHEMISTRY, 6, 1849-1852 [10.1039/b801909f].
Synthesis of imidazolidin-2-one-4-carboxylate and of (tetrahydro)pyrimidin-2-one-5-carboxylate via an efficient modification of the Hofmann rearrangement
ANGELICI, GAETANO;CONTALDI, SIMONE;TOMASINI, CLAUDIA
2008
Abstract
A mild and efficient methodology for the rearrangement of protected asparagine and protected glutamine is reported; good results are obtained with a wide selection of protecting groups.File in questo prodotto:
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