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Results: 1-18 |
Results: 18

Authors: Kumadaki, I Jonoshita, S Sato, K Omote, M Ando, A
Citation: I. Kumadaki et al., Synthesis cyclization of alpha-(trifluoromethyl)pyrrolidines by of N-tosyl-alpha-(trifluoromethyl)homoallylamine derivatives, HETEROCYCLE, 54(2), 2001, pp. 589

Authors: Omote, M Ando, A Sato, K Kumadaki, I
Citation: M. Omote et al., Syntheses of chiral fluorine analogs of hematoporphyrin, TETRAHEDRON, 57(38), 2001, pp. 8085-8094

Authors: Kumadaki, I Ando, A Omote, M
Citation: I. Kumadaki et al., Synthesis of fluorinated analogs of natural porphyrins potentially useful for the diagnosis and therapy of cancer, J FLUORINE, 109(1), 2001, pp. 67-81

Authors: Yano, T Yano, Y Yajima, S Kumadaki, I Ichikawa, T Otani, S Hagiwara, K
Citation: T. Yano et al., The suppression of ornithine decarboxylase expression and cell proliferation at the promotion stage of lung tumorigenesis in mice by alpha-tocopheryloxybutyric acid, BIOCH PHARM, 61(9), 2001, pp. 1177-1181

Authors: Shigeoka, T Kuwahara, Y Watanabe, K Sato, K Omote, M Ando, A Kumadaki, I
Citation: T. Shigeoka et al., Synthesis of fluorine analogs of protoporphyrin potentially useful for diagnosis and therapy of cancer - Part 3. Synthesis of (2,2-difluorovinyl)-trifluorovinyl and (1-chloro-2,2-difluorovinyl)-(2,2-difluorovinyl) deuteroporphyrin, HETEROCYCLE, 52(1), 2000, pp. 383-388

Authors: Yano, T Yajima, S Hagiwara, K Kumadaki, I Yano, Y Otani, S Uchida, M Ichikawa, T
Citation: T. Yano et al., Vitamin E inhibits cell proliferation and the activation of extracellular signal-regulated kinase during the promotion phase of lung tumorigenesis irrespective of antioxidative effect, CARCINOGENE, 21(11), 2000, pp. 2129-2133

Authors: Shigeoka, T Kuwahara, Y Watanabe, K Sato, K Omote, M Ando, A Kumadaki, I
Citation: T. Shigeoka et al., Synthesis of new fluorovinylzinc reagents and their application for synthesis of fluorine analogs of protoporphyrin, J FLUORINE, 103(2), 2000, pp. 99-103

Authors: Sato, K Tamura, M Tamoto, K Omote, M Ando, A Kumadaki, I
Citation: K. Sato et al., Michael-type reaction of ethyl bromodifluoroacetate with alpha,beta-unsaturated carbonyl compounds in the presence of copper powder, CHEM PHARM, 48(7), 2000, pp. 1023-1025

Authors: Kato, M Maeda, K Sato, K Omote, M Ando, A Kumadaki, I
Citation: M. Kato et al., Synthesis of new synthons for organofluorine compounds from halothane containing sulfur functional groups, CHEM PHARM, 48(5), 2000, pp. 683-686

Authors: Ando, A Yamazaki, M Komura, M Sano, Y Hattori, N Omote, M Kumadaki, I
Citation: A. Ando et al., An efficient route to formyldeuteroporphyrins and their Wittig reaction, HETEROCYCLE, 50(2), 1999, pp. 913-918

Authors: Omote, M Kominato, A Sugawara, M Sato, K Ando, A Kumadaki, I
Citation: M. Omote et al., A novel axially dissymmetric ligand with chiral 2,2,2-trifluoro-1-hydroxyethyl groups, TETRAHEDR L, 40(30), 1999, pp. 5583-5585

Authors: Kumadaki, I Jonoshita, S Harada, A Omote, M Ando, A
Citation: I. Kumadaki et al., Synthesis of organofluorine compounds using ene type reaction of N-(p-toluenesulfonyl)trifluoroacetaldehyde imine, J FLUORINE, 97(1-2), 1999, pp. 61-63

Authors: Sakumo, K Kuki, N Kuno, T Takagi, T Koyama, M Ando, A Kumadaki, I
Citation: K. Sakumo et al., Ene-type reaction of trifluoroacetaldehyde hemiacetal with ene compounds in the presence of a Lewis acid, J FLUORINE, 93(2), 1999, pp. 165-170

Authors: Ando, A Kumadaki, I
Citation: A. Ando et I. Kumadaki, Progress on the syntheses of fluorine analogs of natural porphyrins potentially useful for the diagnosis and therapy of certain cancers, J FLUORINE, 100(1-2), 1999, pp. 135-146

Authors: Shigeoka, T Kuwahara, Y Watanabe, K Sato, K Omote, M Ando, A Kumadaki, I
Citation: T. Shigeoka et al., Synthesis of fluorine analogs of protoporphyrin potentially useful for diagnosis and therapy of cancer. IV. Synthesis of(trifluorovinyl)vinyl- and (1-chloro-2,2-difluorovinyl)vinyldeuteroporphyrins, CHEM PHARM, 47(9), 1999, pp. 1326-1329

Authors: Sato, K Kawata, R Ama, F Omote, M Ando, A Kumadaki, I
Citation: K. Sato et al., Synthesis of alkenyl- and aryldifluoroacetate using a copper complex from ethyl bromodifluoroacetate, CHEM PHARM, 47(7), 1999, pp. 1013-1016

Authors: Jonoshita, S Harada, A Omote, M Ando, A Kumadaki, I
Citation: S. Jonoshita et al., Synthesis of organofluorine compounds using the ene reaction of N-(p-toluenesulfonyl)trifluoroacetaldehyde imine, CHEM PHARM, 47(5), 1999, pp. 656-662

Authors: Gu, CG Wysocki, VH Harada, A Takaya, H Kumadaki, I
Citation: Cg. Gu et al., Dissociative and reactive hyperthermal ion-surface collisions with Langmuir-Blodgett films terminated by CF3(CH2)(n)-, n-perfluoroalkyl, or n-alkyl groups, J AM CHEM S, 121(45), 1999, pp. 10554-10562
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