Pregled bibliografske jedinice broj: 838613
Mechanochemical Preparation of 3, 5-Disubstituted Hydantoins from Dipeptides and Unsymmetrical Ureas of Amino Acid Derivatives
Mechanochemical Preparation of 3, 5-Disubstituted Hydantoins from Dipeptides and Unsymmetrical Ureas of Amino Acid Derivatives // Journal of organic chemistry, 81 (2016), 20; 9802-9809 doi:10.1021/acs.joc.6b01832 (međunarodna recenzija, članak, znanstveni)
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Naslov
Mechanochemical Preparation of 3, 5-Disubstituted Hydantoins from Dipeptides and Unsymmetrical Ureas of Amino Acid Derivatives
Autori
Konnert, Laure ; Gonnet, Lori ; Halasz, Ivan ; Suppo, Jean-Simon ; de Figueiredo, Renata Marcia ; Campagne, Jean-Marc ; Lamaty, Fredéric ; Martinez, Jean ; Colacino, Evelina
Izvornik
Journal of organic chemistry (0022-3263) 81
(2016), 20;
9802-9809
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
3 ; 5-disubstituted hydantoins ; mechanochemistry
Sažetak
5-Substituted-3-(alkoxycarbonyl)alkyl-hydantoin derivatives were prepared by mechanochemistry from amino esters or dipeptides, via a 1, 1′-carbonyldiimidazole-mediated one-pot/two-step cyclization reaction involving amino acid unsymmetrical urea A and carboxy-imidazolyl-dipeptide ester B intermediates. Comparative experiments in solution were also performed. The successful preparation of an antibacterial agent precursor was also investigated.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
