Synthesis of some new N-monosubstituted fluoroacetamides

dc.creator	Miščević, S.
dc.creator	Minić, D.
dc.creator	Petrović, Slobodan
dc.date.accessioned	2021-03-10T09:34:47Z
dc.date.available	2021-03-10T09:34:47Z
dc.date.issued	1992
dc.identifier.issn	0022-1139
dc.identifier.uri	http://TechnoRep.tmf.bg.ac.rs/handle/123456789/35
dc.description.abstract	Twenty new N-monosubstituted fluoroacetamides with potential toxicological properties have been synthesized by acylation of the corresponding amines with fluoroacetyl chloride. The substituents were cycloalkyl or various alkyl (with straight or branched carbon chain) groups. The yields ranged from 50 to 92%.	en
dc.relation	Research Fund of Serbia, Belgrade, for financial support. Thanks are also due to Dr G. Hajdukovic for the 13C and ‘H NMR analyses and Mrs Lj. JeremiC for MS examination.
dc.rights	restrictedAccess
dc.source	Journal of Fluorine Chemistry
dc.title	Synthesis of some new N-monosubstituted fluoroacetamides	en
dc.type	article
dc.rights.license	ARR
dc.citation.epage	247
dc.citation.issue	2
dc.citation.other	59(2): 239-247
dc.citation.rank	M23
dc.citation.spage	239
dc.citation.volume	59
dc.identifier.doi	10.1016/S0022-1139(00)82416-1
dc.identifier.pmid
dc.identifier.scopus	2-s2.0-9044254706
dc.type.version	publishedVersion