dc.contributor.author |
Kokotos, G |
en |
dc.contributor.author |
Markidis, T |
en |
dc.contributor.author |
Constantinou-Kokotou, V |
en |
dc.date.accessioned |
2014-06-06T06:43:12Z |
|
dc.date.available |
2014-06-06T06:43:12Z |
|
dc.date.issued |
1996 |
en |
dc.identifier.issn |
00397881 |
en |
dc.identifier.uri |
http://62.217.125.90/xmlui/handle/123456789/1091 |
|
dc.relation.uri |
http://www.scopus.com/inward/record.url?eid=2-s2.0-0029832130&partnerID=40&md5=82cfb0995eae4e824810c57fbe637c72 |
en |
dc.subject.other |
amino acid derivative |
en |
dc.subject.other |
diamine |
en |
dc.subject.other |
polyamine |
en |
dc.subject.other |
article |
en |
dc.subject.other |
chirality |
en |
dc.subject.other |
drug synthesis |
en |
dc.subject.other |
reaction analysis |
en |
dc.subject.other |
stereochemistry |
en |
dc.title |
Synthesis of chiral triamines and diamines from amino acids |
en |
heal.type |
journalArticle |
en |
heal.publicationDate |
1996 |
en |
heal.abstract |
Selectively protected (2S)-1,2,6-triaminohexane 4 was prepared from L-lysine by reduction of the amino acid, replacement of the hydroxy group by an azido group and selective reduction. Following the same method vicinal diamines 11 and 13 bearing a third functional group were synthesized from L-glutamic acid. |
en |
heal.journalName |
Synthesis |
en |
dc.identifier.issue |
10 |
en |
dc.identifier.spage |
1223 |
en |
dc.identifier.epage |
1226 |
en |