Inherently Chiral Azonia[6]helicene-Modified β-Cyclodextrin: Synthesis, Characterization, and Chirality Sensing of Underivatized Amino Acids in Water

Qinfei Huang, Liangwei Jiang, Wenting Liang, Jianchang Gui, Dingguo Xu, Wanhua Wu, Yoshito Nakai, Masaki Nishijima, Gaku Fukuhara, Tadashi Mori, Yoshihisa Inoue, Cheng Yang

Research output: Contribution to journalArticlepeer-review

38 Citations (Scopus)

Abstract

The (P)- and (M)-3-azonia[6]helicenyl β-cyclodextrins exhibit l/d selectivities of up to 12.4 and P/M preferences of up to 28.2 upon complexation with underivatized proteinogenic amino acids in aqueous solution at pH 7.3.

Original languageEnglish
Pages (from-to)3430-3434
Number of pages5
JournalJournal of Organic Chemistry
Volume81
Issue number8
DOIs
Publication statusPublished - 2016 Apr 15
Externally publishedYes

ASJC Scopus subject areas

  • Organic Chemistry

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