Synthesis of 2-monofunctionalized 2,4,6,8-tetraazabicyclo[3.3.0]octane-3,7-diones View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2003-01

AUTHORS

A. N. Kravchenko, E. Yu. Maksareva, P. A. Belyakov, A. S. Sigachev, K. Yu. Chegaev, K. A. Lyssenko, O. V. Lebedev, N. N. Makhova

ABSTRACT

New (1R*,5S*)-2-R-2,4,6,8-tetraazabicyclo[3.3.0]octane-3,7-diones containing the terminal carboxy or hydroxy group in the substituent R were synthesized by cyclocondensation of 4,5-dihydroxyimidazolidin-2-one with 1-R-ureas. Single-crystal X-ray diffraction analysis showed that 2-carboxyethyl-2,4,6,8-tetraazabicyclo[3.3.0]octane-3,7-dione crystallizes as a racemate.

PAGES

192-197

Identifiers

URI

http://scigraph.springernature.com/pub.10.1023/a:1022473004714

DOI

http://dx.doi.org/10.1023/a:1022473004714

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1028978094


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