On the synthesis of new amphiphilic entities by the succinic coupling of [beta]-cyclodextrins to calixarenes

Cyclodextrins (CD) and calixarenes (CAL), two important classes of compounds in inclusion chemistry, demonstrate different, but complementary affinities. CD are hydrophilic and amphiphilic, while CAL are insoluble in water. In search for new methods of construction of amphiphilic species from CDs, t...

Full description

Saved in:
Bibliographic Details
Published inCanadian journal of chemistry Vol. 83; no. 5; p. 493
Main Authors Jankowski, Christopher K, Arseneau, Sébastien, Blu, Jérome, Mauclaire, Laurent, Aychet, Nicolas
Format Journal Article
LanguageEnglish
Published Ottawa Canadian Science Publishing NRC Research Press 01.05.2005
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Cyclodextrins (CD) and calixarenes (CAL), two important classes of compounds in inclusion chemistry, demonstrate different, but complementary affinities. CD are hydrophilic and amphiphilic, while CAL are insoluble in water. In search for new methods of construction of amphiphilic species from CDs, the system of a CD and a CAL-crown coupled together were considered. Jankowski et al report on the synthesis of the CD-CAL-crown compounds, starting with these tetranitro derivatives 4 and 5, and coupling them to beta-CD 3 through a succinic diamide linker.
ISSN:0008-4042
1480-3291