Inherently Chiral Bambus[4]urils

Amar Ramchandra Mohite, Ofer Reany

نتاج البحث: نشر في مجلةمقالةمراجعة النظراء


A new class of bambus[4]urils (BU[4]s) composed of asymmetric N,N′-disubstituted glycoluril subunits with different alkyl groups were designed, synthesized, and fully characterized by NMR techniques and X-ray crystallography. Structural studies showed that four macrocyclic diastereoisomers are possible: two Sn symmetric achiral macrocycles and two macrocycles that are "inherently"chiral. The relative "head-to-tail"arrangement of the N-substituents in Bn4Me4BU[4], 5a, clearly observed by X-ray spectroscopy analysis, determines the overall symmetry of the bambusuril structure. Chiral Pr4Me4BU[4], 4b, was resolved by chiral high-performance liquid chromatography (HPLC) into its enantiomers, and all four inherently chiral bambusuril pairs (two Pr4Me4BU[4] and two Bn4Me4BU[4] stereoisomers, 4b, 4d, 5b, and 5d) were clearly observed by 1H NMR spectroscopy with the aid of (R)-BINOL as a chiral solvating agent. This latter methodology provides a rapid and powerful approach for investigating the enantiopurity of inherently chiral cavitands, which complements and augments the conventional chromatographic approaches.

اللغة الأصليةالإنجليزيّة
الصفحات (من إلى)9190-9200
عدد الصفحات11
دوريةJournal of Organic Chemistry
مستوى الصوت85
رقم الإصدار14
المعرِّفات الرقمية للأشياء
حالة النشرنُشِر - 17 يوليو 2020

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Copyright © 2020 American Chemical Society.


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