Reaction of diethyl 1-acylamino-2,2-dichloroethenylphosphonates with amino acids esters View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2012-04

AUTHORS

K. M. Kondratyuk, E. I. Lukashuk, A. V. Golovchenko, E. B. Rusanov, V. S. Brovarets

ABSTRACT

Reactions of available diethyl 1-acylamino-2,2-dichloroethenylphosphonates with amino acids esters were studied, which in the case of esters of proline, nipecotic and isonipecotic acids resulted in N-substituted derivatives of 5-amino-4-diethoxyphosphoryloxazol in high yields. Their behavior in the acidic and alkaline media was investigated by the example of methyl N-(4-diethoxyphosphoryl-2-R-oxazol-5-yl)isonipecotinate.

PAGES

643-651

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363212040056

DOI

http://dx.doi.org/10.1134/s1070363212040056

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1045502174


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