Synthesis and Some Spectroscopic Properties of Porphyrin Derivatives Connected with Nucleobases (Adenine, Thymine, Guanine and Cytosine)by Alkanamide Chains von HISATOME, Masao, MARUYAMA, Noriaki, IKEDA, Koichi, FURUTERA, Tetsuo, ISHIKAWA, Tomiyasu, YAMAKAWA, Koji

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Synthesis and molecular structure of [45](1,2,3,4,5)ferrocenophane ([4]superferrocenophane) von Hisatome, Masao, Watanabe, Jun, Kawajiri, Yoshiki, Yamakawa, Koji, Iitaka, Yoichi

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Synthesis of [4][34](1,2,3,4,5)ferrocenophane von Watanabe, Jun, Hisatome, Masao, Yamakawa, Koji

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Synthesis and Characterization of Model System in Biological Related Function: Model Compounds for Investigation of Metal-Metal Interaction and Nucleobase-Aromatics Interaction von HISATOME, Masao

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Synthesis and Molecular Structures of [4] Superferrocenophane ([45] (1, 2, 3, 4, 5) Ferrocenophane) and Its Related Compounds von HISATOME, Masao, YAMAKAWA, Koji

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Design of a novel artificial nucleobase for the selective formation of a triple-complex with a cytosine-guanine base pair von Sasaki, Shigeki, Nakashima, Shouji, Nagatsugi, Fumi, Tanaka, Yoshitsugu, Hisatome, Masao, Maeda, Minoru

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ChemInform Abstract: Synthesis and Characterization of Model System in Biologically Related Function - Model Compounds for Investigation of Metal-Metal Interaction and Nucleobase-A... von Hisatome, Masao

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Organometallic compounds. 33. X-ray crystal structure of a tetrabridged ferrocenophane trimer: 6,9,12-trioxo[3.3.3](1,1')[4](2,2')[4](3,3')[4](4,4')[4](5,5')ferrocenophane von Hisatome, Masao, Kawajiri, Yoshiki, Yamakawa, Koji, Mamiya, Kosuke, Harada, Yoshinori, Iitaka, Yoichi

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Mass Spectra of Ferrocenophanes: Ketone Derivatives von HISATOME, MASAO, YAMAKAWA, KOJI

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Intramolecular cyclization reaction of 1,1′-bis-(α-hydroxyisopropyl)ferrocene von Hisatome, Masao, Yamakawa, Koji

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Bridged ferrocenes : VII. Synthesis of di- and tri-bridged ferrocenes with pentamethylne chains von Hisatome, Masao, Hillman, Manny

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I-I-NMR Spectra and Reaction of [n]Frrocenophan-6-ols and -7-ols in Triflu oroacetic Acid -Formation of Ferrocenophane 6-Carbocations von HISATOME, Masao, YAMAKAWA, Koji

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1H-NMR spectra and reaction of [n] frrocenophan-6-ols and -7-ols in trifluoroacetic acid. Formation of ferrocenophane 6-carbocations von HISATOME, Masao, YAMAKAWA, Koji

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生体関連機能に関するモデル系の合成と性質: 金属間相互作用及び核酸塩基-芳香族化合物相互作用のモデル化合物 von 久留, 正雄

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[45](1,2,3,4,5)Ferrocenophane: superferrocenophane von Hisatome, Masao, Watanabe, Jun, Yamakawa, Koji, Iitaka, Yoichi

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Studies of the active complex of a soluble catalyst. I. Ti(O-n-Bu)4-AlEt3 system von Takeda, Masatami, Iimura, Kazuyoshi, Nozawa, Yasuo, Hisatome, Masao, Koide, Naoyuki

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Bridged ferrocenes von Hisatome, Masao, Hillman, Manny

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Organometallic compounds : XII. stereochemical interconversion reactions between 1,1′−bis(α-hydroxyalkyl)ferrocenes and 7-oxa[3]ferrocenophanes von Yamakawa, Koji, Hisatome, Masao

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Synthesis and molecular structure of (4 sub 5 )(1,2,3,4,5)ferrocenophane ((4)superferrocenophane) von Hisatome, Masao, Watanabe, Jun, Kawajiri, Yoshiki, Yamakawa, Koji, Iitaka, Yoichi

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Organometallic compounds : XXVI. Ferrocenophane-7-carbocations and their rearrangement von Hisatome, Masao, Yamakawa, Koji

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