Synthesis of macrocyclic cage compounds by diamine-dihalide one-step coupling reaction

Citation
N. Kon et al., Synthesis of macrocyclic cage compounds by diamine-dihalide one-step coupling reaction, J ORG CHEM, 65(12), 2000, pp. 3708-3715
Citations number
40
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
00223263 → ACNP
Volume
65
Issue
12
Year of publication
2000
Pages
3708 - 3715
Database
ISI
SICI code
0022-3263(20000616)65:12<3708:SOMCCB>2.0.ZU;2-N
Abstract
Macropolycyclic cage compounds were synthesized by a direct reaction betwee n diamines and bis(bromomethyl) compounds. The procedure for constructing t he polycyclic cage structure is simple and straightforward. The macropolycy clic compounds obtainable from this cyclization procedure are three-dimensi onal cage compounds, and any other isomers were not obtained except for two examples. Benzene, pyridine, and aliphatic units could be introduced into the cage structure. The macrocycles that have strong cation affinity were o btained as their potassium complexes.