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J-GLOBAL ID：201702241990869557   Reference number：17A1952100

Why do the Togni reagent and some of its derivatives exist in the high-energy hypervalent iodine form? New insight into the origins of their kinetic stability

Togni試薬とそのいくつかの誘導体が何故高エネルギー超原子価ヨウ素形で存在するのか?速度論的安定性の起源への新しい洞察【Powered by NICT】

Author (3)： Koichi Shungo (Department of Systems and Mathematical Science, Nanzan University, Nagoya, Japan. [e-mail]) ,  Leuthold Benjamin ,  Luethi Hans P.
Material： Physical Chemistry Chemical Physics  (PCCP)
Volume： 19  Issue： 48  Page： 32179-32183  Publication year： 2017 
JST Material Number： A0271C  ISSN： 1463-9076  CODEN： PPCPFQ  Document type： Article
Article type： 短報  Country of issue： United Kingdom (GBR)  Language： ENGLISH (EN)

Abstract/Point： In a recent study published in...

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Thesaurus term： *reagent ,  *stability ,  analogical material ,  *aromatic iodine compound ,  structure ,  oxygen heterocyclic compound ,  polynuclear aromatic compound ,  isomerization ,  *potential barrier ,  transition state ,  electrophilic reaction ,  group(radical) ,  iodine ,  internuclear distance
Semi thesaurus term： *Togni's Reagent ,  *kinetic stability ,  *hypervalent iodine compound ,  basic structure ,  isobenzofuran derivative ,  substituent

JST classification (3)： Condensed derivatives of furan  (CF07073M) ,  Cyclization reaction,ring-opening reaction  (CF02050I) ,  Gevmetry of molecules in general  (BH05021S)

Terms in the title (7)： Togni試薬 ,  誘導体 ,  高エネルギー ,  超原子価ヨウ素 ,  速度論的安定性 ,  起源 ,  洞察