@article{ace1fc91cff3451296d435d953a209bb,
title = "Asymmetric autocatalysis triggered by triglycine sulfate with switchable chirality by altering the direction of the applied electric field",
abstract = "Triglycine sulfate (TGS) acts as a chiral trigger for asymmetric autocatalysis with amplification of enantiomeric excess,i.e., the Soai reaction. Therefore, molecular chirality of highly enantioenriched organic compounds is controlled by a ferroelectric crystal TGS, whose polarization is altered by an electric field.",
author = "Tsuneomi Kawasaki and Yoshiyasu Kaimori and Seiya Shimada and Natsuki Hara and Susumu Sato and Kenta Suzuki and Toru Asahi and Arimasa Matsumoto and Kenso Soai",
note = "Funding Information: The authors thank Yuko Araki, Kunihiko Hatase and Koichi Abe for the preliminary experiments. This work has been financially supported by Grant-in-Aid for Scientific Research from Japan Society for the Promotion of Science (JSPS KAKENHI Grant Numbers 23685012, 26810026, 15H03781, 18H04518, 19K05482 and 19K22190, Grant-in-Aid for JSPS Research Fellow to Y. K. Number 15J03968) and by MEXT-Supported Program for the Strategic Research Foundation at Private Universities, 2012–2016. Publisher Copyright: {\textcopyright} The Royal Society of Chemistry 2021.",
year = "2021",
month = jun,
day = "21",
doi = "10.1039/d1cc02162a",
language = "English",
volume = "57",
pages = "5999--6002",
journal = "Chemical Communications",
issn = "1359-7345",
publisher = "Royal Society of Chemistry",
number = "49",
}