Chiral alpha,omega-diaminoethers derived from D-mannitol and L-treitol as building blocks for the synthesis of macrocyclic compounds possessing 1,3-benzenedicarboxamide or 2,6-pyridinedicarboxamide subunits

Authors
Piatek, P Gruza, MM Jurczak, J
Citation
P. Piatek et al., Chiral alpha,omega-diaminoethers derived from D-mannitol and L-treitol as building blocks for the synthesis of macrocyclic compounds possessing 1,3-benzenedicarboxamide or 2,6-pyridinedicarboxamide subunits, TETRAHEDR-A, 12(12), 2001, pp. 1763-1769
Citations number
32
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
12
Issue
12
Year of publication
2001
Pages
1763 - 1769
Database
ISI
SICI code
0957-4166(20010716)12:12<1763:CADFDA>2.0.ZU;2-1
Abstract
Three new chiral alpha,omega -diaminoethers, derivatives Of D-mannitol and L-treitol, possessing C-2 symmetry are prepared. The alpha,omega -diaminoet hers were applied to the macrocyclization reaction under non-high-dilution conditions, which afforded chiral macrocyclic diamides possessing either 2, 6-pyridinedicarboxamide or 1,3-benzenedicarboxamide moieties. (C) 2001 Else vier Science Ltd. All rights reserved.