共 69 条
Squaramides: physical properties, synthesis and applications
被引:493
作者:

Storer, R. Ian
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h-index: 0
机构:
Pfizer Global Res & Dev, Worldwide Med Chem, Sandwich CT13 9NJ, Kent, England Pfizer Global Res & Dev, Worldwide Med Chem, Sandwich CT13 9NJ, Kent, England

Aciro, Caroline
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Pfizer Global Res & Dev, Worldwide Med Chem, Sandwich CT13 9NJ, Kent, England Pfizer Global Res & Dev, Worldwide Med Chem, Sandwich CT13 9NJ, Kent, England

Jones, Lyn H.
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Pfizer Global Res & Dev, Chem Biol Grp, Sandwich CT13 9NJ, Kent, England Pfizer Global Res & Dev, Worldwide Med Chem, Sandwich CT13 9NJ, Kent, England
机构:
[1] Pfizer Global Res & Dev, Worldwide Med Chem, Sandwich CT13 9NJ, Kent, England
[2] Pfizer Global Res & Dev, Chem Biol Grp, Sandwich CT13 9NJ, Kent, England
关键词:
URGE URINARY-INCONTINENCE;
SQUARIC ACID;
RECEPTOR ANTAGONISTS;
ASYMMETRIC REDUCTION;
BINDING-SITE;
DESIGN;
POTENT;
AROMATICITY;
DERIVATIVES;
3-HYDROXY-3-CYCLOBUTENE-1,2-DIONE;
D O I:
10.1039/c0cs00200c
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Squaramides are remarkable four-membered ring systems derived from squaric acid that are able to form up to four hydrogen bonds. A high affinity for hydrogen bonding is driven through a concomitant increase in aromaticity of the ring. This hydrogen bonding and aromatic switching, in combination with structural rigidity, have been exploited in many of the applications of squaramides. Substituted squaramides can be accessed via modular synthesis under relatively mild or aqueous conditions, making them ideal units for bioconjugation and supramolecular chemistry. In this tutorial review the fundamental electronic and structural properties of squaramides are explored to rationalise the geometry, conformation, reactivity and biological activity.
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页码:2330 / 2346
页数:17
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