An inherently chiral calix[4]crown carboxylic acid in the partial cone conformation

2012 ◽  
Vol 77 (1-4) ◽  
pp. 327-335 ◽  
Author(s):  
Jiao Shi ◽  
Si-Zhe Li ◽  
Yu-Xiang Xia ◽  
Xiao-Gang Wang ◽  
Jun Luo ◽  
...  
2016 ◽  
Vol 52 (11) ◽  
pp. 2366-2369 ◽  
Author(s):  
Petr Slavík ◽  
Michal Kohout ◽  
Stanislav Böhm ◽  
Václav Eigner ◽  
Pavel Lhoták

Regioselective mercuration of calix[4]arene in the partial cone conformation enabled a straightforward access to a novel type of inherently chiral calixarenes with a highly distorted cavity.


2005 ◽  
Vol 70 (19) ◽  
pp. 7662-7671 ◽  
Author(s):  
Ru Miao ◽  
Qi-Yu Zheng ◽  
Chuan-Feng Chen ◽  
Zhi-Tang Huang

2012 ◽  
Vol 74 (1-4) ◽  
pp. 277-284 ◽  
Author(s):  
Yu-Xiang Xia ◽  
Hao-Hui Zhou ◽  
Jiao Shi ◽  
Si-Zhe Li ◽  
Min Zhang ◽  
...  

1993 ◽  
Vol 46 (11) ◽  
pp. 1673 ◽  
Author(s):  
LT Byrne ◽  
JM Harrowfield ◽  
DCR Hockless ◽  
BJ Peachey ◽  
BW Skelton ◽  
...  

The hydroxide ion catalysed phosphorylation of p-t- butylcalix [4] arene by diethyl chlorophosphate under heterogeneous conditions shows a marked sensitivity to the nature of the phase transfer catalyst used. Thus, substitution of tetraethylammonium bromide for the tetrabutylammonium bromide prescribed for the synthesis of the calixarene tetraphosphate leads to a major reaction product becoming a bis (phosphate) in which the calixarene binds as a unidentate ligand to one phosphorus and as a bidentate ligand to the other. An X-ray crystal structure analysis on this new compound shows the calixarene to adopt a somewhat distorted 'cone' conformation with an unusual orientation of one of the t-butyl substituents into the cone cavity. It also reveals that a significant diastereoselectivity must operate in the formation reaction. The only other reaction product detected in this system appears to be the calixarene tetraphosphate in a partial cone conformation.


1994 ◽  
Vol 47 (6) ◽  
pp. 1185 ◽  
Author(s):  
JM Harrowfield ◽  
M Mocerino ◽  
BW Skelton ◽  
CR Whitaker ◽  
AH White

The synthesis and room-temperature single-crystal X-ray structural characterization of 25,27- di(allyloxy)-5,17-di-t-butyl-26,28-dimethoxycalix[4]arene are recorded. Crystals are monoclinic, C2/c, a 29.089(5), b 10.742(2), c 26.218(8) Ǻ, β 110.09(2)°, Z = 8; the structure was refined to a residual of 0.065 for 4103 independent 'observed' [I > 3σ(I)] reflections. The flattened partial cone conformation of the molecule allows inclusion of one of the methoxy substituents in a way which could block inclusion of a metal ion capable of polyhapto aromatic coordination and which may therefore explain why solution n.m.r. measurements indicate that silver(I) binds to the pendent alkene groups.


2013 ◽  
Vol 26 (4) ◽  
pp. 295-305 ◽  
Author(s):  
Paula M. Marcos ◽  
Filipa A. Teixeira ◽  
Manuel A. P. Segurado ◽  
José R. Ascenso ◽  
Raul J. Bernardino ◽  
...  

2005 ◽  
Vol 11 (20) ◽  
pp. 5917-5928 ◽  
Author(s):  
Jun Luo ◽  
Qi-Yu Zheng ◽  
Chuan-Feng Chen ◽  
Zhi-Tang Huang

2013 ◽  
Vol 37 (1) ◽  
pp. 220-227 ◽  
Author(s):  
Oldřich Hudeček ◽  
Jan Budka ◽  
Hana Dvořáková ◽  
Petra Cuřínová ◽  
Ivana Císařová ◽  
...  

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