Hexagonal crystalline inclusion complexes of 4-iodophenoxy trimesoate

2008 ◽  
pp. 4726 ◽  
Author(s):  
F. Christopher Pigge ◽  
Venu R. Vangala ◽  
Pradeep P. Kapadia ◽  
Dale C. Swenson ◽  
Nigam P. Rath
RSC Advances ◽  
2021 ◽  
Vol 11 (22) ◽  
pp. 13091-13096
Author(s):  
Lu Chen ◽  
Yanbin Huang

Guest polymers have significant influence on the dissolution of drug–polymer inclusion complex crystals.


2002 ◽  
Vol 35 (9) ◽  
pp. 3778-3780 ◽  
Author(s):  
Xintao Shuai ◽  
Francis E. Porbeni ◽  
Min Wei ◽  
Todd Bullions ◽  
Alan E. Tonelli

2007 ◽  
Vol 48 (3) ◽  
pp. 540-546 ◽  
Author(s):  
O. V. Andreeva ◽  
B. F. Garifullin ◽  
A. T. Gubaidullin ◽  
V. A. Al’fonsov ◽  
V. E. Kataev ◽  
...  

Chirality ◽  
1989 ◽  
Vol 1 (2) ◽  
pp. 137-141 ◽  
Author(s):  
Heng L. Jin ◽  
Apryll Stalcup ◽  
Daniel W. Armstrong

2001 ◽  
Vol 73 (7) ◽  
pp. 1137-1145 ◽  
Author(s):  
Fumio Toda

Hexaol host compounds which include guest molecules maximum in 1:6 ratio were prepared. Aromatic hexaol host, hexahydroxytriphenylene, was found to form chiral inclusion crystal by complexation with achiral guest molecules. Some interesting and important optical resolutions of rac-guests by inclusion complexation with a chiral host were described. When chemical reaction and the inclusion complexation procedures in a water suspension medium are combined, new economical and ecological method of the preparation of optically active compound can be established. When photochemical reactions are carried out in an inclusion crystal with a chiral host, enantioselective reactions occur, and optically active product can be obtained. Several successful reactions are described.


2003 ◽  
Vol 6 (3) ◽  
pp. 137-144 ◽  
Author(s):  
Samat A Talipov ◽  
Fatkhulla Kh Tadjimukhamedov ◽  
Juerg Hulliger ◽  
Bakhtiyar T Ibragimov ◽  
Abdurasul Yuldashev

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