MISC

1991年1月

ENDO SELECTIVE CYCLIZATIONS OF SELENONIUM ION INTERMEDIATE - EFFICIENT FORMATION OF 1-HALO-3-SELENO-CYCLOHEXANES

TETRAHEDRON LETTERS
  • T KATAOKA
  • ,
  • M YOSHIMATSU
  • ,
  • H SHIMIZU
  • ,
  • M HORI

32
1
開始ページ
105
終了ページ
108
記述言語
英語
掲載種別
DOI
10.1016/S0040-4039(00)71230-5
出版者・発行元
PERGAMON-ELSEVIER SCIENCE LTD

Selenoacetal 1 was cyclized with tin(IV) chloride in the 6-Endo-Trig mode to give 1-chloro-3-methylselenocyclohexanes (2a,b) regio- and stereoselectively. Bromo- or iodocyclohexane derivatives were afforded by use of tin(IV) bromide or titanium(IV) iodide, respectively.


リンク情報
DOI
https://doi.org/10.1016/S0040-4039(00)71230-5
CiNii Articles
http://ci.nii.ac.jp/naid/80005634221
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:A1991ER38500027&DestApp=WOS_CPL

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