@article{e8f2ff787e874080954bc996a45593ab,
title = "Inherently Chiral Azonia[6]helicene-Modified β-Cyclodextrin: Synthesis, Characterization, and Chirality Sensing of Underivatized Amino Acids in Water",
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.",
author = "Qinfei Huang and Liangwei Jiang and Wenting Liang and Jianchang Gui and Dingguo Xu and Wanhua Wu and Yoshito Nakai and Masaki Nishijima and Gaku Fukuhara and Tadashi Mori and Yoshihisa Inoue and Cheng Yang",
note = "Funding Information: This work was supported by the National Natural Science Foundation of China (Nos. 21372165, 21321061, 21402129, and 21572142), State Key Laboratory of Polymer Materials Engineering, Grant No. sklpme2014-2-06, Japan Society for the Promotion of Science (Nos. 26620030, 26620061, 25620163, 24655025, and 23350018), Mitsubishi Chemical Corporation Fund, Sumitomo Foundation, Shorai Foundation, Kurata Foundation, Tokuyama Foundation, and Iketani Foundation, which is gratefully acknowledged.",
year = "2016",
month = apr,
day = "15",
doi = "10.1021/acs.joc.6b00130",
language = "English",
volume = "81",
pages = "3430--3434",
journal = "Journal of Organic Chemistry",
issn = "0022-3263",
publisher = "American Chemical Society",
number = "8",
}