Affiliation:
1. Department of Chemistry and Center for Emerging Material and Advanced Devices National Taiwan University No. 1, Sec. 4, Roosevelt Road Taipei Taiwan
Abstract
AbstractIn situ switching of the associated anions of a rotaxane catalyst between Cl− and TFPB− exposes its dialkylammonium and imidazolium stations, respectively, thereby selectively catalyzing the reactions of a mixture of trans‐cinnamaldehyde and an aliphatic thiol to yield the Michael adduct and the thioacetal product, respectively.
Funder
National Science and Technology Council
National Taiwan University
Subject
General Chemistry,Catalysis
Cited by
1 articles.
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