Synthesis of NMs-DACN: Small and hydrophilic click reaction device

Yuuya Kawasaki; Yuki Yamanaka; Yuki Seto; Kazunobu Igawa; Katsuhiko Tomooka

doi:10.1246/cl.190026

Synthesis of NMs-DACN: Small and hydrophilic click reaction device

Yuuya Kawasaki, Yuki Yamanaka, Yuki Seto, Kazunobu Igawa, Katsuhiko Tomooka

分子集積化学部門

研究成果: ジャーナルへの寄稿 › 学術誌 › 査読

12 被引用数 (Scopus)

抄録

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.

本文言語	英語
ページ（範囲）	495-497
ページ数	3
ジャーナル	Chemistry Letters
巻	48
号	5
DOI	https://doi.org/10.1246/cl.190026
出版ステータス	出版済み - 2019

!!!All Science Journal Classification (ASJC) codes

化学一般

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10.1246/cl.190026

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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",

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year = "2019",

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journal = "Chemistry Letters",

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TY - JOUR

T1 - Synthesis of NMs-DACN

T2 - Small and hydrophilic click reaction device

AU - Kawasaki, Yuuya

AU - Yamanaka, Yuki

AU - Seto, Yuki

AU - Igawa, Kazunobu

AU - Tomooka, Katsuhiko

PY - 2019

Y1 - 2019

N2 - 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.

AB - 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.

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DO - 10.1246/cl.190026

M3 - Article

AN - SCOPUS:85066114687

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Synthesis of NMs-DACN: Small and hydrophilic click reaction device

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!!!All Science Journal Classification (ASJC) codes

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