著者

青山豊太郎 編

出版者

精行舎

巻号頁・発行日

vol.初編, 1892

著者

青山 豊

出版者

一般社団法人 表面技術協会

雑誌

実務表面技術 (ISSN:03682358)

巻号頁・発行日

vol.20, no.5, pp.251-255, 1973-05-01 (Released:2009-10-30)

被引用文献数

1

著者

青山 豊

出版者

一般社団法人 表面技術協会

雑誌

実務表面技術 (ISSN:03682358)

巻号頁・発行日

vol.20, no.2, pp.97-100, 1973-02-01 (Released:2009-10-30)

著者

青山 豊

出版者

同志社大学

雑誌

同志社アメリカ研究 (ISSN:04200918)

巻号頁・発行日

vol.42, pp.149-167, 2006

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研究ノート

著者

青山 豊彦 塩入 孝之

出版者

公益社団法人 日本薬学会

雑誌

YAKUGAKU ZASSHI (ISSN:00316903)

巻号頁・発行日

vol.115, no.6, pp.446-459, 1995-06-25 (Released:2008-05-30)

参考文献数

22

被引用文献数

3 5

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Tilivalline (1a), a metabolite isolated from Klebsiella pneumoniae var. oxytoca, belongs to a group of pyrrolo [2, 1-c] [1, 4] benzodiazepines, a characteristic skeleton of anthramycin-type antitumor antibiotics. We have accomplished a completely stereoselective, efficient and convenient synthesis of 1a utilizing a new Mannich type intramolecular cyclization as a key step. Further, a computational chemical analysis clarified the effect of zinc chloride on the high stereoselectivity in the tilivalline synthesis. To aim both the extension of the scope of the new Mannich type intramolecular cyclization and the studies on the structure-biological activity relationship, we further extended the method to the synthesis of tilivalline derivatives and 2-(3'-indolyl)-1, 4-benzodiazepines (50). Investigation on the cytotoxicity of 1a and its analogs has revealed that 1a shows the strong cytotoxicity toward mouse leukemia L 1210 cells and the replacement of the indole function of 1a with cyano one increases the cytotoxicity of 1a about 100 times (IC50=0.05 μg/ml).

著者

青山 豊彦 塩入 孝之

出版者

公益社団法人日本薬学会

雑誌

藥學雜誌 = Journal of the Pharmaceutical Society of Japan (ISSN:00316903)

巻号頁・発行日

vol.115, no.6, pp.446-459, 1995-06-25

参考文献数

22

被引用文献数

5

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Tilivalline (1a), a metabolite isolated from Klebsiella pneumoniae var. oxytoca, belongs to a group of pyrrolo [2, 1-c] [1, 4] benzodiazepines, a characteristic skeleton of anthramycin-type antitumor antibiotics. We have accomplished a completely stereoselective, efficient and convenient synthesis of 1a utilizing a new Mannich type intramolecular cyclization as a key step. Further, a computational chemical analysis clarified the effect of zinc chloride on the high stereoselectivity in the tilivalline synthesis. To aim both the extension of the scope of the new Mannich type intramolecular cyclization and the studies on the structure-biological activity relationship, we further extended the method to the synthesis of tilivalline derivatives and 2-(3'-indolyl)-1, 4-benzodiazepines (50). Investigation on the cytotoxicity of 1a and its analogs has revealed that 1a shows the strong cytotoxicity toward mouse leukemia L 1210 cells and the replacement of the indole function of 1a with cyano one increases the cytotoxicity of 1a about 100 times (IC<SUB>50</SUB>=0.05 &mu;g/ml).

著者

張 功幸 塩入 孝之 青山 豊彦

出版者

社団法人 有機合成化学協会

雑誌

有機合成化学協会誌 (ISSN:00379980)

巻号頁・発行日

vol.67, no.4, pp.357-368, 2009 (Released:2011-04-11)

被引用文献数

1 8

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This review describes the recent application of trimethylsilyldiazomethane (Me3SiCHN2, TMSCHN2), its lithium and magnesium bromide salts [TMSC(Li)N2 and TMSC(MgBr)N2] to the synthesis of heterocycles. Reaction of TMSCHN2 with acyl isocyanates followed by Diels-Alder reaction with propiolates or N-phenylmaleimide affords furans or bicyclic pyridones in a one-pot process, respectively. In addition, TMSCHN2 is useful for the preparation of 2-azaazulenes, aziridines and indolizines. Meanwhile, TMSC(Li)N2 reacts with benzynes generated from halobenzenes to yield 3-trimethylsilylindazoles, which are easily converted to 1-arylindazoles or indazoles bearing 3-hydroxymethyl units. TMSC(Li)N2 is also applicable to the synthesis of indoles, benzofurans, pyrroles, thiophenes and 2,3-benzodiazepines. By using TMSC(MgBr)N2, α-substituted β-trimethylsilyl-α,β-epoxyesters can be synthesized from α-ketoesters in a one-pot process. Reaction of TMSC(MgBr)N2 with carbonyl compounds efficiently furnishes trimethylsilylated diazoalcohols, which react with propiolates to give di- or tri-substituted pyrazoles.