The synthesis of 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea leads to only one of the two possible diastereomers, which has been found to be in the E-configuration by X-ray analysis.

On the stereochemistry of the synthesis of 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea and its E-configuration crystal structure / L., Greci; P., Carloni; O., Mandrioli; Righi, Lara; Rizzoli, Corrado; Sgarabotto, Paolo. - In: JOURNAL OF CHEMICAL RESEARCH. SYNOPSES. - ISSN 0308-2342. - (2003), pp. 655-657. [10.3184/030823403322655987]

On the stereochemistry of the synthesis of 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea and its E-configuration crystal structure

RIGHI, Lara;RIZZOLI, Corrado;SGARABOTTO, Paolo
2003

Abstract

The synthesis of 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea leads to only one of the two possible diastereomers, which has been found to be in the E-configuration by X-ray analysis.
On the stereochemistry of the synthesis of 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea and its E-configuration crystal structure / L., Greci; P., Carloni; O., Mandrioli; Righi, Lara; Rizzoli, Corrado; Sgarabotto, Paolo. - In: JOURNAL OF CHEMICAL RESEARCH. SYNOPSES. - ISSN 0308-2342. - (2003), pp. 655-657. [10.3184/030823403322655987]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/1460868
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