Literature DB >> 21399835

Squaramides: physical properties, synthesis and applications.

R Ian Storer1, Caroline Aciro, Lyn H Jones.   

Abstract

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.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21399835     DOI: 10.1039/c0cs00200c

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  29 in total

Review 1.  Recent advances in the molecular design of synthetic vaccines.

Authors:  Lyn H Jones
Journal:  Nat Chem       Date:  2015-12       Impact factor: 24.427

2.  Lewis acid enhancement by hydrogen-bond donors for asymmetric catalysis.

Authors:  Steven M Banik; Anna Levina; Alan M Hyde; Eric N Jacobsen
Journal:  Science       Date:  2017-11-10       Impact factor: 47.728

3.  Thiosquaramides: pH switchable anion transporters.

Authors:  Nathalie Busschaert; Robert B P Elmes; Dawid D Czech; Xin Wu; Isabelle L Kirby; Evan M Peck; Kevin D Hendzel; Scott K Shaw; Bun Chan; Bradley D Smith; Katrina A Jolliffe; Philip A Gale
Journal:  Chem Sci       Date:  2014-09-01       Impact factor: 9.825

4.  Pyrocinchonimides Conjugate to Amine Groups on Proteins via Imide Transfer.

Authors:  Mark B Richardson; Kristin N Gabriel; Joseph A Garcia; Shareen N Ashby; Rebekah P Dyer; Joshua K Kim; Calvin J Lau; John Hong; Ryan J Le Tourneau; Sanjana Sen; David L Narel; Benjamin B Katz; Joseph W Ziller; Sudipta Majumdar; Philip G Collins; Gregory A Weiss
Journal:  Bioconjug Chem       Date:  2020-04-30       Impact factor: 4.774

5.  Novel rapidly diversifiable antimicrobial RNA polymerase switch region inhibitors with confirmed mode of action in Haemophilus influenzae.

Authors:  Ed T Buurman; Melinda A Foulk; Ning Gao; Valerie A Laganas; David C McKinney; Demetri T Moustakas; Jonathan A Rose; Adam B Shapiro; Paul R Fleming
Journal:  J Bacteriol       Date:  2012-07-27       Impact factor: 3.490

6.  Exploring the potential of diarylacetylenediols as hydrogen bonding catalysts.

Authors:  Yunus E Türkmen; Viresh H Rawal
Journal:  J Org Chem       Date:  2013-08-14       Impact factor: 4.354

Review 7.  Put a ring on it: application of small aliphatic rings in medicinal chemistry.

Authors:  Matthias R Bauer; Paolo Di Fruscia; Simon C C Lucas; Iacovos N Michaelides; Jennifer E Nelson; R Ian Storer; Benjamin C Whitehurst
Journal:  RSC Med Chem       Date:  2021-01-07

8.  Asymmetric synthesis of highly functionalized tetrahydropyrans via a one-pot organocatalytic Michael/Henry/ketalization sequence.

Authors:  Robert Hahn; Gerhard Raabe; Dieter Enders
Journal:  Org Lett       Date:  2014-06-27       Impact factor: 6.005

9.  Scaffold diversity for enhanced activity of glycosylated inhibitors of fungal adhesion.

Authors:  Harlei Martin; Tara Somers; Mathew Dwyer; Ryan Robson; Frederick M Pfeffer; Ragnar Bjornsson; Tobias Krämer; Kevin Kavanagh; Trinidad Velasco-Torrijos
Journal:  RSC Med Chem       Date:  2020-08-17

10.  Selection of a novel anti-nicotine vaccine: influence of antigen design on antibody function in mice.

Authors:  David C Pryde; Lyn H Jones; David P Gervais; David R Stead; David C Blakemore; Matthew D Selby; Alan D Brown; Jotham W Coe; Matthew Badland; David M Beal; Rebecca Glen; Yvonne Wharton; Gavin J Miller; Phil White; Ningli Zhang; Michelle Benoit; Karen Robertson; James R Merson; Heather L Davis; Michael J McCluskie
Journal:  PLoS One       Date:  2013-10-01       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.