Formation of p-aminostyrene cyclic tetramer

Citation
T. Hamaya et al., Formation of p-aminostyrene cyclic tetramer, CHEM LETT, (6), 2001, pp. 570-571
Citations number
27
Categorie Soggetti
Chemistry
Journal title
CHEMISTRY LETTERS
ISSN journal
03667022 → ACNP
Issue
6
Year of publication
2001
Pages
570 - 571
Database
ISI
SICI code
0366-7022(20010605):6<570:FOPCT>2.0.ZU;2-E
Abstract
Two isomers (1a and 1b) of p-aminostyrene cyclic tetramer (1,9,17,25-tetram ethyl-2,10,18,26-tetraaza[2,2,2.2]paracyclophane, 1) were produced from the linear oligomer P, by passing it through a silica gel column. These are st ereochemical isomers (1a: RSRS, meso and 1b: RRSS, meso) and stable in solu tion. They include two solvent molecules in their crystalline states; 1a in cludes benzene and Ib includes ethanol.