Lifeng Zhang

TL;DR: The Staudinger reaction was applied for the first time in the immobilization of mono-(6-azido-6-deoxy)-perfunctionalised cyclodextrins onto the surface of aminised silica gel under mild conditions as discussed by the authors.

TL;DR: A novel chiral stationary phase (PPHCDN7) was prepared by immobilization of heptakis(6-azido-6-deoxy-2,3-di-O-phenylcarbamoylated)-beta-cyclodextrin onto the surface of amino-functionalized silica gel via multiple urea linkages derived from an extended application of the Staudinger reaction.

TL;DR: The Staudinger reaction was applied to the facile synthetic generation of a series of mono-6-alkylcarbamido- 6-deoxy-perfunctionalised cyclodextrins and mono-8-ω-alkenyl carbamido -6-de oxygen-per functionalised cyclodesxtrin compounds to afford reactive siloxane intermediates which can be immobilised onto silica gel for application as an efficient chiral stationary phase for enantioseparation

TL;DR: In this paper, the Staudinger reaction was used for enantioseparation of racemic mixtures using atropine, bendroflumethiazide and four β-adrenergic blocking agents under reversed phase conditions.

TL;DR: In this paper, two novel pendant hand-basket type calixarene gas chromatography stationary phases were prepared by hydrosilylation of ω-undecenyloxymethyl dimethyl calix[4]-15C5 and ωundecnyloxyclic oxymethyl-15C6 with dichloromethane followed by condensation reaction with silanol-terminated polydimethylsiloxane.