Art

J-GLOBAL ID：200902240286709365   Reference number：04A0296605

Oligomerization of N-Tosylindole with Aluminum Chloride

塩化アルミニウムを用いたN-トシルインドールのオリゴメリゼーション

Author (4)： FUJINO K (Gifu Univ., Gifu, JPN) ,  YANASE E (Gifu Univ., Gifu, JPN) ,  SHINODA Y (Gifu Univ., Gifu, JPN) ,  NAKATSUKA S (Gifu Univ., Gifu, JPN)
Material： Bioscience, Biotechnology, and Biochemistry  (Bioscience Biotechnology & Biochemistry)
Volume： 68  Issue： 3  Page： 764-766  Publication year： Mar. 23, 2004 
JST Material Number： G0021A  ISSN： 0916-8451  CODEN： BBBIEJ  Document type： Article
Article type： 短報  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： polynuclear aromatic compound ,...

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JST classification (1)： Addition reaction,elimination reaction  (CF02030M)

Substance index (13)： Indole ,  1-Tosyl-1H-indole ,  1,1′-Ditosyl-2,3-dihydro-3,3′-bi[1H-indole] ,  1,1′-Ditosyl-2,3-dihydro-2,3′-bi[1H-indole] ,  3,3′-[2-(Tosylamino)phenethylidene]bis(1-tosyl-1H-indole) ,  1,1′-Ditosyl-2,3-dihydro-3,4′-bi[1H-indole] ,  1,1′-Ditosyl-2,3-dihydro-3,5′-bi[1H-indole] ,  1,1′-Ditosyl-2,3-dihydro-3,6′-bi[1H-indole] ,  1,1′-Ditosyl-2,3-dihydro-2,4′-bi[1H-indole] ,  1,1′-Ditosyl-2,3-dihydro-2,5′-bi[1H-indole] ,  1,1′-Ditosyl-2,3-dihydro-2,6′-bi[1H-indole] ,  1,1′-Ditosyl-3,3′-bi[1H-indole] ,  3,3′-Biindole

Reference (23)：

• 1) Sundberg, R. J., “The Chemistry of Indoles”, Academic Press, New York, 1–447 (1970).
• 2) Nakatsuka, S., Miyazaki, H., and Goto, T., Synthetic studies on natural products containing oxidized diketopiperazine. I. Total synthesis of (±)-neoechinulin A, an indole alkaloid containing oxidized diketopiperazine. Tetrahedron Lett., 21, 2817–2820 (1980).
• 3) Nakatsuka, S., Miyazaki, H., and Goto, T., Regiospecific cyclization of N-benzoyl-N-(methoxymethyl)-1-methyl-α,β-dehydrotryptophan methyl ester to a 5,6-dihydroazepino[5,4,3-cd]indole derivative. A new method for introducing substituents on to the 4-position of the indole nucleus. Chem. Lett., 407–410 (1981).
• 4) Nakatsuka, S., Yamada, K., and Goto, T., Introduction of a substituent on to the 4-position of an indole nucleus by intermolecular cyclization of α,β-dehydrotryptophan methyl ester with an aldehyde. Tetrahedron Lett., 27, 4757–4758 (1986).
• 5) Nakatsuka, S., Asano, O., and Goto, T., Regiospecific cyclization of 3-carbomethoxyindole-1-propanoic acid on to 7-position of the indole nucleus. Heterocycles, 24, 2109–2110 (1986).

Terms in the title (2)： 塩化アルミニウム ,  オリゴメリゼーション