Literature DB >> 10508352

Supramolecular Isomerism in Caviplexes.

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Abstract

Stereoisomeric complexes of an open-ended cavitand and its guest molecules (shown schematically) were detected, and complexes within caviplexes were introduced. Some control can be exerted on the stereoisomerism through methylation of the guest. The symbols "0" and "1" represent different ends of the guest molecule.

Year:  1999        PMID： 10508352     DOI： 10.1002/(sici)1521-3773(19990903)38:17<2600::aid-anie2600>3.0.co;2-t

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


  4 in total

Review 1.  Artificial Molecular Machines.

Authors:  Sundus Erbas-Cakmak; David A Leigh; Charlie T McTernan; Alina L Nussbaumer
Journal:  Chem Rev       Date:  2015-09-08       Impact factor: 60.622

2.  Adjusting the binding thermodynamics, kinetics, and orientation of guests within large synthetic hydrophobic pockets.

Authors:  C L D Gibb; X Li; B C Gibb
Journal:  Proc Natl Acad Sci U S A       Date:  2002-04-16       Impact factor: 11.205

3.  Electronic and steric effects in binding of deep cavitands.

Authors:  Richard J Hooley; Siddhartha R Shenoy; Julius Rebek
Journal:  Org Lett       Date:  2008-12-04       Impact factor: 6.005

4.  Pseudo-capsule assemblies characterized by 19F NMR techniques.

Authors:  Agustí Lledó; Per Restorp; Julius Rebek
Journal:  J Am Chem Soc       Date:  2009-02-25       Impact factor: 15.419
  4 in total

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