MISC

2000年6月

Synthesis of macrocyclic cage compounds by diamine-dihalide one-step coupling reaction

JOURNAL OF ORGANIC CHEMISTRY
  • N Kon
  • ,
  • H Takemura
  • ,
  • K Otsuka
  • ,
  • K Tanoue
  • ,
  • S Nakashima
  • ,
  • M Yasutake
  • ,
  • K Tani
  • ,
  • J Kimoto
  • ,
  • T Shinmyozu
  • ,
  • T Inazu

65
12
開始ページ
3708
終了ページ
3715
記述言語
英語
掲載種別
DOI
10.1021/jo991911y
出版者・発行元
AMER CHEMICAL SOC

Macropolycyclic cage compounds were synthesized by a direct reaction between diamines and bis(bromomethyl) compounds. The procedure for constructing the polycyclic cage structure is simple and straightforward. The macropolycyclic compounds obtainable from this cyclization procedure are three-dimensional cage compounds, and any other isomers were not obtained except for two examples. Benzene, pyridine, and aliphatic units could be introduced into the cage structure. The macrocycles that have strong cation affinity were obtained as their potassium complexes.

リンク情報
DOI
https://doi.org/10.1021/jo991911y
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000087609100018&DestApp=WOS_CPL
ID情報
  • DOI : 10.1021/jo991911y
  • ISSN : 0022-3263
  • Web of Science ID : WOS:000087609100018

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