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J-GLOBAL ID：201702283676962602   Reference number：17A1410343

Reaction of 2-propargylphenylcarbamates with diphenyliodonium salts via Meyer-Schuster rearrangement

Meyer-Schuster転位を経由する2-プロパルギルフェニルカルバマートとジフェニルヨードニウム塩との反応【Powered by NICT】

Author (6)： Minami Hideki (Faculty of Pharmaceutical Sciences, Hiroshima International University, 5-1-1 Hirokoshingai, Kure, Hiroshima 737-0112, Japan) ,  Okamoto Noriko (Faculty of Pharmaceutical Sciences, Hiroshima International University, 5-1-1 Hirokoshingai, Kure, Hiroshima 737-0112, Japan) ,  Sueda Takuya (Faculty of Pharmaceutical Sciences, Hiroshima International University, 5-1-1 Hirokoshingai, Kure, Hiroshima 737-0112, Japan) ,  Sakaguchi Takatsugu (Faculty of Pharmaceutical Sciences, Hiroshima International University, 5-1-1 Hirokoshingai, Kure, Hiroshima 737-0112, Japan) ,  Ishikura Minoru (School of Pharmaceutical Sciences, Health Sciences University of Hokkaido, Ishikari-Tobetsu, Hokkaido 061-0293, Japan) ,  Yanada Reiko (Faculty of Pharmaceutical Sciences, Hiroshima International University, 5-1-1 Hirokoshingai, Kure, Hiroshima 737-0112, Japan)
Material： Tetrahedron Letters  (Tetrahedron Lett)
Volume： 58  Issue： 45  Page： 4277-4280  Publication year： Nov. 08, 2017 
JST Material Number： E0366A  ISSN： 0040-4039  Document type： Article
Article type： 短報  Country of issue： United Kingdom (GBR)  Language： ENGLISH (EN)

Abstract/Point： The syntheses of 2,3-dihydro-4...

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Thesaurus term： rearrangement reaction ,  Michael reaction ,  *carbamate ,  acetylenic compound ,  unsaturated alcohol ,  organoiodine compound ,  nitrogen heterocyclic compound ,  polynuclear aromatic compound ,  Friedel-Crafts reaction ,  Alkylation ,  conjugated diene ,  alicyclic compound ,  one-pot synthesis ,  asymmetric synthesis ,  Friedel-Crafts alkylation ,  *Meyer-Schuster rearrangement ,  *Quinolones ,  iodonium compound ,  Indenes
Semi thesaurus term： Michael addition ,  indene derivative ,  one-pot reaction

Author keywords (5)： Quinolone ,  Meyer-Schuster rearrangement ,  Michael addition ,  Indenone ,  Friedel-Crafts alkylation

JST classification (1)： Quinolines,isoquinolines  (CF07096H)

Substance index (6)： 3α-Phenyl-4-oxo-3,4-dihydroquinoline-1(2H)-carboxylic acid ethyl ester ,  2β-Isobutyl-3α-phenyl-4-oxo-3,4-dihydroquinoline-1(2H)-carboxylic acid ethyl ester ,  2β-Methyl-3α-phenyl-4-oxo-3,4-dihydroquinoline-1(2H)-carboxylic acid ethyl ester ,  2β,3α-Diphenyl-4-oxo-3,4-dihydroquinoline-1(2H)-carboxylic acid ethyl ester ,  (1,1-Dimethyl-2-phenyl-3-oxoindan-4-yl)carbamic acid ethyl ester ,  (2-Phenyl-3-oxospiro[indan-1,1′-cyclopentane]-4-yl)carbamic acid ethyl ester

Terms in the title (3)： Meyer-Schuster転位 ,  ジフェニルヨードニウム ,  塩