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Chemical Compound Review:

ETHYLENEUREA imidazolidin-2-one

Synonyms: Ethylene urea, SureCN9827, I601_ALDRICH, CHEMBL12034, SureCN16730, ...

Engel, Y. et al., Lihs, F.J. et al., Maeda, H. et al., Lee, S.G. et al.

Lee, Zhang, Song, Lee, Choi,

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High impact information on ETHYLENEUREA

Interactions of these compounds with urea, thiourea, 1,3-dimethylurea, tetrahydropyrimidin-2(1H)-one, imidazolidin-2-one, and selected uronium salts were assessed by three-dimensional excitation-emission spectroscopy, UV-vis absorbance, and fluorescence titrations [1].
Novel 1,4-diphosphanes with imidazolidin-2-one backbones as chiral ligands: highly enantioselective Rh-catalyzed hydrogenation of enamides [2].
Synthesis and central nervous system actions of thyrotropin-releasing hormone analogs containing a 1-substituted 2-oxoimidazolidine moiety [3].

Analytical, diagnostic and therapeutic context of ETHYLENEUREA

Proton and (13)C NMR and isotope-dependent FTIR measurements confirmed that carboxylation had occurred at the nitrogen atom of 2-imidazolidone to give 2(-) [4].

References

Phenanthroline-derived ratiometric chemosensor for ureas. Engel, Y., Dahan, A., Rozenshine-Kemelmakher, E., Gozin, M. J. Org. Chem. (2007) [Pubmed]
Novel 1,4-diphosphanes with imidazolidin-2-one backbones as chiral ligands: highly enantioselective Rh-catalyzed hydrogenation of enamides. Lee, S.G., Zhang, Y.J., Song, C.E., Lee, J.K., Choi, J.H. Angew. Chem. Int. Ed. Engl. (2002) [Pubmed]
Synthesis and central nervous system actions of thyrotropin-releasing hormone analogs containing a 1-substituted 2-oxoimidazolidine moiety. Maeda, H., Suzuki, M., Sugano, H., Yamamura, M., Ishida, R. Int. J. Pept. Protein Res. (1989) [Pubmed]
Kinetics and mechanism for CO(2) scrambling in a N-carboxyimidazolidone analogue for N(1)-carboxybiotin. Lihs, F.J., Caudle, M.T. J. Am. Chem. Soc. (2002) [Pubmed]

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