HETEROCYCLES
An International Journal for Reviews and Communications in Heterocyclic ChemistryWeb Edition ISSN: 1881-0942
Published online by The Japan Institute of Heterocyclic Chemistry
Regular Issue
Vol. 23, No. 1, 1985
Published online:
■ Selective Halogenation of 4-Oxo-4,5,6,7-tetrahydroindoles to 5-Halo-4,5,6,7-tetrahydeoindoles with Copper(II) Halides
Masakatsu Matsumoto,* Yasuko Ishoda, and Nobuko Watanabe
*Sagami Central Research Center, 4-4-1 Nishi-Ohnuma, Sagamihara, Kanagawa 229-0012, Japan
Abstract
Halogenation of 4-oxo-4,5,6,7-tetrahydroindoles with copper(II) bromide or copper(II) chloride gave selectively 5-halo-4-oxo-4,5,6,7-tetrahydroindoles, which were easily transformed to 4-hydroxyindoles by the action of lithium halide/lithium carbonate in dimethylformamide.
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■ The Reaction of Enones with N-Subatituted Hydrazines and N-Substituted Ureas
Choji Kashima* and Nobutoshi Yoshiwara
*Department of Chemistry, University of Tsukuba, 1-1-1 Ten-nodai, Tsukuba-shi, Ibaraki, 305-8571, Japan
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■ Oxidation of Indoles with Molybdenumperoxo Complex, MoO5·HMPA
Tomomi Kawasaki, Chun-Sheng Chien, Takako Suzuki, Toshikatsu Takanami, and Masanori Sakamoto
*Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan
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■ Pericyclic Reactions of Pyridine N-Oxides
Takuzo Hisano, Kazunobu Harano, Toshikazu Matsuoka, Ryuichi Fukuoka, Motoji Murase, and Hirotoshi Yamada
*Faculty of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-hon-machi, Kumamoto 862-0973, Japan
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■ Selective Reactions of Active Methyl Groups on Pyridine and Quinoline Rings
Hiroshi Yamanaka, Takao Sakamoto, Hiroshi Yoshizawa, and Sumiko Nishimura
*Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-8578, Japan
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■ Reactions of Quinoline N-Oxides and Nitrobenzenes with Methylquinoline and -Pyridine Derivatives in the Presence of t-BuOK
Genji Iwasaki, Seitaro Saeki, Kazuko Wada, and Masatomo Hamana
*Faculty of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan
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■ Neighboring Group Participation by Pyridine Rings and N-Oxides. Synthesis and Reactions of 5,8-Dihydro-5,8-methanoisoquinoline Derivatives
Tadashi Irie, Yoko Hayashi, and Hiroshi Tanida
*Shionogi Research Laboratories, Shionogi & Co. Ltd., Fukushima-ku, Osaka 553-0002, Japan
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■ A Convenient Preparation of Bipyridine Derivatives
Tsutomu Kawai, Naomichi Furukawa, and Shigeru Oae
*Department of Chemistry, University of Tsukuba, 1-1-1 Ten-nodai, Tsukuba-shi, Ibaraki, 305-8571, Japan
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■ A New Method for α-Substitution in Nitrogen-containing Heterocycles
Norihiro Tokitoh, Renji Okazaki, and Naoki Inamoto
*Department of Chemistry, School of Science, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
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■ Synthesis of β-Lactams Using the Photochemical Reaction of 4-Oxygenated 2-Pyridone Derivatives
Nobuya Katagiro, Masayuki Sato, Makoto Muto, Toshiyuki Sakamoto, Satoshi Saikawa, Chikara Kaneko, Toshihiko Naito, and Akemi Saito
*Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-8578, Japan
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■ Synthesis and Properties of Cyclophane Containing Hetero Aromatic. II. 13-Substituted [2.2]Metacyclo(3,5)pyridinophanes
Toshihide Kawashima, Yasuo Tohda, Masahiro Ariga, Yutaka Mori, and Shoichi Misumi
*Department of Chemistry, Faculty of Science, Osaka City University, Sugimoto, Sumiyoshi-ku, Osaka 558-8585, Japan
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■ Synthesis of the Host Molecule Having Crown Ether and Cyclophane Units
Masayuki Takada, Masataka Kubo, Akira Youda, Kazuhiko Saigo, and Masaki Hasegawa
*Department of Synthetic Chemistry, Faculty of Engineering, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan
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■ Synthesis of Fluorine Containing Pyrroles and Their Derivatives
Hiroo Toi, Michihide Homma, Hiroyuki Onda, Katsuhiro Aoyagi, Yasuhiro Aoyama, and Hisanobu Ogoshi
*Department of Material Science, Technological University of Nagaoka, Kamitomioka, Nagaoka, Niigata 949-54, Japan
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■ Basicity and Redox-character of Pyrrole[3,2-b]pyrrole and Its Related Compounds
Tsutomu Kumagai, Shoji Tanaka, Kyosuke Satake, and Toshio Mukai
*Pharmaceutical Institute, Tohoku University, Aobayama, Sendai 980-8578, Japan
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■ Reaction of Pyridinium or Isoquinolinium Ketene Dithioacetals with Aromatic N-Imines or S-Imines
Yoshinori Tominaga, Takeharu Michioka, Yukio Oniyama, Hiroto Goto, Yoshiro Matsuda, and Goro Kobayashi (deceased)
*Faculty of Pharmaceutical Sciences, Nagasaki University, 1-14, Bunkyo-machi, Nagasaki 852-8521, Japan
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■ Reissert Type’s Reaction by Use of Phosphite (II)
Isao Takeuchi, Yasuhiro Shibata, and Yoshiki Hamada
*Faculty of Pharmacy, Meijo University, 150 Yagotoyama, Tenpaku, Nagoya 468-8503, Japan
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■ Synthesis of 2-Substituted Dihydropyrimidines and Their Properties
Choji Kashima, Masao Shimizu, and Yoshimori Omote
*Department of Chemistry, University of Tsukuba, 1-1-1 Ten-nodai, Tsukuba-shi, Ibaraki, 305-8571, Japan
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■ Introduction of C-Group into the Pyrazine Ring with Organoaluminium Compounds
Akihiro Ohta, Akira Inoue, Masakatsu Ohta, Tokuhiro Watanabe, and Yasuo Akita
*Tokyo University of Pharmacy and Life Science, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan
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■ Cyclic Peroxides. 11. Chemiluminescent Reaction Mechanism of N-Methyl-9-(dicarboalkoxymethyl)acridanes
Nobutaka Suzuki, Mitsumasa Nakaminami, Toshio Tsukamoto, Kathuhiko Iwasaki, and Yasuji Izawa
*Faculty of Engineering, Mie University, 1515 Uehama-cho, Tsu, Mie 514-5807, Japan
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■ Photochemical Synthesis of Spiro-β-Lactams
Masazumi Ikeda, Takamasa Uchino, Midori Yamano, Hiroyuki Ishibashi, Yasumitsu Tamura, and Masaru Kido
*Kyoto Pharmaceutical University, Misasagi-Shichonocho, Yamashina, Kyoto 607-8414, Japan
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■ Ring-transformation Reactions of Azaheteromodified Adamantanes and Related Derivatives
Koji Asai, Shoji Eguchi, and Tadashi Sasaki
*Faculty of Engineering, Nagoya University, Chikusa, Nagoya, Aichi 464-8601, Japan
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■ [3+2]Cycloaddition Utilizing the Charactaristics of Organic Silicon Compounds — Study on Regio- and Stereoselectivity of Pyrrolidine Ring Formation
Nobuyuki Imai, Hiromi Kotaki, Yoshiyasu Terao, and Kazuo Achiwa
*Schol of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Shizuoka 422-8526, Japan
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■ Stereoselective Synthesis of Pyrrolidines by Intramolecular Haloamidation
Yoshinao Tamaru, Shinichi Kawamura, Kunitada Tanaka, and Zenichi Yoshida
*Faculty of Engineering, Kyoto University, Yoshida, Sakyou-ku, Kyoto 606-8501, Japan
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■ Synthesis of Heterocycles via Vinyl Cations
Tsugio Kitamura, Shinjiro Kobayashi, and Hiroshi Taniguchi
*Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan
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■ Syntheses of Diazepines from Pyridine Azides
Hiroyuki Sawanishi, Kayoko Tajima, Makoto Osada, and Takashi Tsuchiya
*School of Pharmacy, Hokuriku University, 3-Ho, Kanagawa machi, Kanazawa 920-1181, Japan
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■ The Reactions of Nitrene for the Conjugated π-Systems
Kyosuke Satake, Hiroshi Mizushima, Masaru Kimura, and Shiro Morosawa
*Department of Chemistry, Faculty of Science, Okayama University, 3-1-1 Tsushima-naka, Okayama 700-8530, Japan
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■ Stereochemical Aspects of 1,3-Dipolar Cycloaddition Reactions of Heterocyclic N-Ylides to Olefinic Dipolarophiles
Otohiko Tsuge, Shuji Kanemasa, and Shigeori Takenaka
*Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan
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■ Synthesis of Aziridine Derivative from α-Silyl Carbanion and Their Mutagenicity
Takeo Konakahara, Masayuki Matsuki, Kenji Sato, Yoshiharu Hisamatsu, and Hidetsuru Matsushita
*Department of Industrial Chemistry, Faculty of Science and Technology, Science University of Tokyo, 2641 Yamazaki, Noda, Chiba 278-8510, Japan
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■ Synthesis of Tricyclic Compounds Using 2(1H)-Quinoxalinone Derivatives
Kenji Makino, Gozyo Sakata, Katsushi Morimoto, and Yoshinori Ochiai
*Central Research Institute, Nissan Chemical Industries Ltd., 722-1 Tsuboicho, Funabashi, Chiba 274-8507, Japan
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■ Synthesis of Novel Quinoxalinyl-1,5-benzodiazepines by Ring Transformation
Yoshihisa Kurasawa and Atsushi Takada
*School of Pharmaceutical Sciences, Kitasato University, Kitasato University