Concepedia

Exclusive enantioselective recognition of glucopyranosides by inherently chiral hemicryptophanes

Olivier Perraud, Alexandre Martinez, Jean‐Pierre Dutasta

Chemical Communications · 2011 · 53 citations · 26 references

DOI

Concepts

Abstract

Inherently chiral hemicryptophanes were used to complex β- and α-glucoside derivatives with high diastereo- and enantio-selectivity. In most cases, the exclusive recognition by the M-hemicryptophane enantiomers was observed.

References

26

EQNMR: a computer program for the calculation of stability constants from nuclear magnetic resonance chemical shift data

Michael J. Hynes · Journal of the Chemical Society Dalton Transactions · 1993 · 837 citations

, , +12

Polyol Recognition by a Steroid-Capped Porphyrin. Enhancement and Modulation of Misfit Guest Binding by Added Water or Methanol

Richard P. Bonar‐Law, Jeremy K. M. Sanders · Journal of the American Chemical Society · 1995 · 224 citations

, , +7

A New Family of Chiral Binaphthyl‐Derived Cyclophane Receptors: Complexation of Pyranosides

S. Anderson, Ulf Neidlein, Völker Gramlich et al. · Angewandte Chemie International Edition in English · 1995 · 149 citations

, , +12

Diastereomeric Recognition of Chiral Foldamer Receptors for Chiral Glucoses

Chuang Li, Gui-Tao Wang, Hui‐Ping Yi et al. · Organic Letters · 2007 · 122 citations

, , +15

<i>Speleands</i>. Macropolycyclic receptor cages based on binding and shaping sub‐units. Synthesis and properties of macrocycle cyclotriveratrylene combinations. Preliminary communication

Josette Canceill, André Collet, Jacqueline Gabard et al. · Helvetica Chimica Acta · 1982 · 91 citations

, , +15