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Pregled bibliografske jedinice broj: 420554

Absolute stereochemistry of alloxanic acid. A configurational relay for uricase reaction


Modrić, Nevenka; Poje, Mirko; Watkin, D. J.; Edwards, A. J.
Absolute stereochemistry of alloxanic acid. A configurational relay for uricase reaction // Tetrahedron letters, 34 (1993), 29; 4679-4682 doi:10.1016/S0040-4039(00)60655-X (međunarodna recenzija, članak, znanstveni)


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Naslov
Absolute stereochemistry of alloxanic acid. A configurational relay for uricase reaction

Autori
Modrić, Nevenka ; Poje, Mirko ; Watkin, D. J. ; Edwards, A. J.

Izvornik
Tetrahedron letters (0040-4039) 34 (1993), 29; 4679-4682

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
alloxanic acid ; enantiomorphic esters ; X-ray ; (+)-(R)-alloxanic acid ; (-)-(S)-5-hydroxyisourate ; conversion ; mechanism ; allantoin

Sažetak
Alloxanic acid was resolved by means of brucine and converted into its enantiomorphic esters and amides, ethyl(-)-alloxanate whose absolute (S)-configuration was established by X-ray analysis served as configurational standard for the correlation of (+)-(R)-alloxanic acid and its precursor (-)-(S)-5-hydroxyisourate, the key uricolytic intermediate.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekti:
1-07-220

Ustanove:
Prirodoslovno-matematički fakultet, Zagreb

Profili:

Avatar Url Nevenka Poje (autor)

Avatar Url Mirko Poje (autor)

Poveznice na cjeloviti tekst rada:

doi www.sciencedirect.com

Citiraj ovu publikaciju:

Modrić, Nevenka; Poje, Mirko; Watkin, D. J.; Edwards, A. J.
Absolute stereochemistry of alloxanic acid. A configurational relay for uricase reaction // Tetrahedron letters, 34 (1993), 29; 4679-4682 doi:10.1016/S0040-4039(00)60655-X (međunarodna recenzija, članak, znanstveni)
Modrić, N., Poje, M., Watkin, D. & Edwards, A. (1993) Absolute stereochemistry of alloxanic acid. A configurational relay for uricase reaction. Tetrahedron letters, 34 (29), 4679-4682 doi:10.1016/S0040-4039(00)60655-X.
@article{article, author = {Modri\'{c}, Nevenka and Poje, Mirko and Watkin, D. J. and Edwards, A. J.}, year = {1993}, pages = {4679-4682}, DOI = {10.1016/S0040-4039(00)60655-X}, keywords = {alloxanic acid, enantiomorphic esters, X-ray, (+)-(R)-alloxanic acid, (-)-(S)-5-hydroxyisourate, conversion, mechanism, allantoin}, journal = {Tetrahedron letters}, doi = {10.1016/S0040-4039(00)60655-X}, volume = {34}, number = {29}, issn = {0040-4039}, title = {Absolute stereochemistry of alloxanic acid. A configurational relay for uricase reaction}, keyword = {alloxanic acid, enantiomorphic esters, X-ray, (+)-(R)-alloxanic acid, (-)-(S)-5-hydroxyisourate, conversion, mechanism, allantoin} }
@article{article, author = {Modri\'{c}, Nevenka and Poje, Mirko and Watkin, D. J. and Edwards, A. J.}, year = {1993}, pages = {4679-4682}, DOI = {10.1016/S0040-4039(00)60655-X}, keywords = {alloxanic acid, enantiomorphic esters, X-ray, (+)-(R)-alloxanic acid, (-)-(S)-5-hydroxyisourate, conversion, mechanism, allantoin}, journal = {Tetrahedron letters}, doi = {10.1016/S0040-4039(00)60655-X}, volume = {34}, number = {29}, issn = {0040-4039}, title = {Absolute stereochemistry of alloxanic acid. A configurational relay for uricase reaction}, keyword = {alloxanic acid, enantiomorphic esters, X-ray, (+)-(R)-alloxanic acid, (-)-(S)-5-hydroxyisourate, conversion, mechanism, allantoin} }

Časopis indeksira:


  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


Citati:





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