SYNTHESIS OF CARBAMATE-PROTECTED SPERMIDINE HOMOLOGS THROUGH ALKANE-ALPHA,OMEGA-DIAMINES

Authors
JOAO M ARAUJO SMP RAGNARSSON U JOAQUINA M TRIGO SAA ALMEIDA MLS
Citation
M. Joao et al., SYNTHESIS OF CARBAMATE-PROTECTED SPERMIDINE HOMOLOGS THROUGH ALKANE-ALPHA,OMEGA-DIAMINES, Journal of chemical research. Synopses, (8), 1996, pp. 366-367
Citations number
23
Categorie Soggetti
Chemistry
Journal title
Journal of chemical research. Synopses → ACNP
ISSN journal
03082342
Issue
8
Year of publication
1996
Pages
366 - 367
Database
ISI
SICI code
0308-2342(1996):8<366:SOCSHT>2.0.ZU;2-Q
Abstract
The total synthesis of three triamines selectively protected in the pr imary amino groups [BocNH(CH2)(n)NHCH(2)CH(2)CH(2)NHZ, n = 3-5] (1a-c) and two triamines protected in the secondary amino function and in on e of the primary amino functions [EtOCONH(CH2)(n)N(Boc)CH2CH2CH2NH2, n =3 and 5] (2a and 2c), based on a simple and efficient procedure, is d escribed.