@article{ff8e9515e2544ebe9c951c5552aa4d2a,
title = "Synthesis of NMs-DACN: Small and hydrophilic click reaction device",
abstract = "Newly designed small and hydrophilic click reaction devices, NMs-4, 8-diazacyclononynes (NMs-DACNs), have been efficiently synthesized by a one-pot double Nicholas approach. NMs-DACNs react with azides smoothly under copper-free conditions and show higher water solubility than that of previously developed NTs-DACNs.",
author = "Yuuya Kawasaki and Yuki Yamanaka and Yuki Seto and Kazunobu Igawa and Katsuhiko Tomooka",
note = "Funding Information: This research was supported by JSPS KAKENHI Grants JP16H04113 and JP18H04419 in Middle Molecular Strategy, the Cooperative Research Program {"}NJRC Mater. & Dev.{"}, and Tokuyama Science Foundation. We thank T. Nishi (IMCE in Kyushu Univ.) for assistance with the HRMS measurements. Funding Information: This research was supported by JSPS KAKENHI Grants JP16H04113 and JP18H04419 in Middle Molecular Strategy, the Cooperative Research Program “NJRC Mater. & Dev.”, and Tokuyama Science Foundation. We thank T. Nishi (IMCE in Kyushu Univ.) for assistance with the HRMS measurements. Publisher Copyright: {\textcopyright} 2019 The Chemical Society of Japan.",
year = "2019",
doi = "10.1246/cl.190026",
language = "English",
volume = "48",
pages = "495--497",
journal = "Chemistry Letters",
issn = "0366-7022",
publisher = "The Chemical Society of Japan",
number = "5",
}