Chiral recognition of alpha-phenylethylamine by sucrose-based macrocyclic receptors.

Chiral recognition of alpha-phenylethylamine by sucrose-based macrocyclic receptors.

Chemical communications (Cambridge, England) (2008-12-03)

Bartosz Lewandowski, Slawomir Jarosz

ZUSAMMENFASSUNG

Simple chiral aza-crown ethers based on sucrose display high enantioselectivity in complexation of phenylethylammonium chlorides.

MATERIALIEN

Produktnummer

Marke

Produktbeschreibung

Sigma-Aldrich

(S)-(−)-α-Methylbenzylamin, 98%

Sigma-Aldrich

(R)-(+)-α-Methylbenzylamin, 98%

Sigma-Aldrich

α-Methylbenzylamin, 99%

Sigma-Aldrich

(R)-(+)-α-Methylbenzylamin, ChiPros^®, produced by BASF, ≥99.0%

Sigma-Aldrich

(R)-(+)-α-Methylbenzylamin, purum, ≥98.0% (sum of enantiomers, GC)

Supelco

(R)-(+)-α-Methylbenzylamin, for chiral derivatization, LiChropur^™, ≥99.0%