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Synergetic effects in the enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylic acid mediated by β-cyclodextrin–pillar[5]arene-hybridized hosts

Jiecheng Ji, Wanhua Wu, Xueqin Wei, Ming Rao, Da‐Yang Zhou, Guo Cheng, Qiyong Gong, Kui Luo, Cheng Yang

2020Chemical Communications29 citationsDOI

Abstract

Tri-cavity hosts consisting of one pillar[5]arene (P5) sandwiched by two β-cyclodextrins (CDs) were synthesized, and their diastereoseparation was successfully accomplished. Photocyclodimerization of 2-anthracenecarboxylate with these hybrid hosts demonstrated the critical dependence of stereoselectivity on the absolute configuration of the central P5 and the conjugating positions on the β-CD, and gave the non-classical HT photodimers in up to 87% ee.

Topics & Concepts

PillarCyclodextrinStereoselectivityChemistryStereochemistryOrganic chemistryCatalysisStructural engineeringEngineeringSupramolecular Chemistry and ComplexesChemical Synthesis and AnalysisAnalytical Chemistry and Chromatography
Synergetic effects in the enantiodifferentiating photocyclodimerization of 2-anthracenecarboxylic acid mediated by β-cyclodextrin–pillar[5]arene-hybridized hosts | Litcius