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dc.contributor.authorJadidi, K
dc.contributor.authorGhahremanzadeh, R
dc.contributor.authorAsgari, D
dc.contributor.authorEslami, P
dc.contributor.authorArvin-Nezhad, H
dc.date.accessioned2018-08-26T08:27:42Z
dc.date.available2018-08-26T08:27:42Z
dc.date.issued2008
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/51222
dc.description.abstractThe green reaction of isatoic anhydrides with alpha-amino acids in presence of the ionic liquid 1-butyl-3-methylimidazolium bromide afforded 1,4-benzodiazepine-2,5-diones in excellent yields in absence of a catalyst. The reaction workup is simple and the ionic liquid was easily recovered from the reaction and reused. The methodology was quite general and a range of cyclic and acyclic alpha-amino acids were examined to produce 1,4-benzodiazepine-2,5-diones.
dc.language.isoEnglish
dc.relation.ispartofMONATSHEFTE FUR CHEMIE
dc.subject1,4-benzodiazepine-2,5-diones
dc.subjectalpha-amino acids
dc.subjectionic liquid
dc.subjectisatoic anhydride
dc.titleEco-friendly synthesis of 1,4-benzodiazepine-2,5-diones in the ionic liquid [bmim]Br
dc.typeArticle
dc.citation.volume139
dc.citation.issue10
dc.citation.spage1229
dc.citation.epage1232
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1007/s00706-008-0922-4


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