Vinamidinium salts of N-substituted aminoacetic acids View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-05

AUTHORS

V. A. Valiullin, T. E. Ivakhnenko, G. S. Borodkin, Sh. G. Mkoyan, S. M. Aldoshin, E. P. Ivakhnenko

ABSTRACT

Formylation of N-phthaloylglycine with the POCl3-DMF system afforded N,N,N′, N′-tetramethyl-2-(N-phthaloyl)vinamidinium perchlorate (2). X-ray diffraction study showed that molecule 2 is planar and contains two equivalent nitrogen atoms in the three-carbon vinamidinium fragment. Salt 2 undergoes transamination with primary aromatic amines to give the corresponding bis-azomethines. The reactions with hydrazines produce substituted 4-aminopyrazoles. More... »

PAGES

860-864

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11172-006-0343-7

DOI

http://dx.doi.org/10.1007/s11172-006-0343-7

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1018988606


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