dc.contributor.author |
Hamilakis, S |
en |
dc.contributor.author |
Tsolomitis, A |
en |
dc.date.accessioned |
2014-03-01T01:18:38Z |
|
dc.date.available |
2014-03-01T01:18:38Z |
|
dc.date.issued |
2003 |
en |
dc.identifier.issn |
0040-4039 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/15122 |
|
dc.subject |
2-amino-3-cyano-2-pyrrolin-4-ones |
en |
dc.subject |
Aminoacetylmalononitriles |
en |
dc.subject |
CDI |
en |
dc.subject |
Tautomers |
en |
dc.subject.classification |
Chemistry, Organic |
en |
dc.subject.other |
2 amino 3 cyano 2 pyrrolin 4 one |
en |
dc.subject.other |
amino acid |
en |
dc.subject.other |
aminoacetonitrile |
en |
dc.subject.other |
aminoacetylmalononitrile |
en |
dc.subject.other |
carbene |
en |
dc.subject.other |
carbonyl derivative |
en |
dc.subject.other |
carbonyl diimidazole |
en |
dc.subject.other |
chemical compound |
en |
dc.subject.other |
enol |
en |
dc.subject.other |
glycine derivative |
en |
dc.subject.other |
imidazole derivative |
en |
dc.subject.other |
malononitrile |
en |
dc.subject.other |
prodrug |
en |
dc.subject.other |
unclassified drug |
en |
dc.subject.other |
acylation |
en |
dc.subject.other |
article |
en |
dc.subject.other |
chemical parameters |
en |
dc.subject.other |
chemical procedures |
en |
dc.subject.other |
drug synthesis |
en |
dc.subject.other |
isolation procedure |
en |
dc.title |
An efficient synthesis of 2-amino-3-cyano-2-pyrrolin-4-ones, via the corresponding open chain tautomers (aminoacetylmalononitriles) |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1016/S0040-4039(03)00730-5 |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1016/S0040-4039(03)00730-5 |
en |
heal.language |
English |
en |
heal.publicationDate |
2003 |
en |
heal.abstract |
Malononitrile has been found to be acylated effectively using N-protected glycines by simultaneous activation of an amino acid carbonyl group and a malononitrile methylene group using carbonyl diimidazole (CDI). The corresponding aminoacetonitriles were isolated as enols and/or as their tautomeric forms, 2-amino-3-cyano-2-pyrrolin-4-ones. (C) 2003 Elsevier Science Ltd. All rights reserved. |
en |
heal.publisher |
PERGAMON-ELSEVIER SCIENCE LTD |
en |
heal.journalName |
Tetrahedron Letters |
en |
dc.identifier.doi |
10.1016/S0040-4039(03)00730-5 |
en |
dc.identifier.isi |
ISI:000182573300022 |
en |
dc.identifier.volume |
44 |
en |
dc.identifier.issue |
19 |
en |
dc.identifier.spage |
3821 |
en |
dc.identifier.epage |
3823 |
en |