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Jun Yano, Takaaki Tanaka
1988 Volume 17 Issue 12 Pages
1943-1946
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Poly(
N,
N-dimethylaniline)(PDA) is a semiconductor having positively charged sites in the polymeric backbone. A PDA coated electrode can capture I
− electrostatically and the I
− in the PDA film can also be oxidized electrochemically. Poly(
o-chloroaniline)(PCA) responses to dissolved I
− selectively, though it is quite an insulator. A PDA/PCA dual-layer coated electrode shows selective Nernstian response to dissolved I
−.
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Kahee Fujita, Atsuo Matsunaga, Hatsuo Yamamura, Taiji Imoto
1988 Volume 17 Issue 12 Pages
1947-1950
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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6
A-
S-phenyl-6
F-
O-(β-naphthalenesulfonyl)-6
X-
O-(p-toluenesulfonyl)-6
A-thio-β-cyclodextrins (X = B, X = C, X = D, X = E, and X = G) were prepared from the reaction of 6
A-S-phenyl-6
F-
O-(β-naphthalenesulf onyl)-6
A-thio-β-cyclodextrin with
p-toluenesulfonyl chloride in pyridine. The structures were determined through their Taka amylase A-catalyzed hydrolyses.
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Tsugio Kitamura, Takashi Kabashima, Shinjiro Kobayashi, Hiroshi Tanigu ...
1988 Volume 17 Issue 12 Pages
1951-1954
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Addition of alkoxide ions resulted in ipso substitution in the photolysis of an alcohol solution of 1-(
p-methoxyphenyl)-2,2-diphenylvinyl bromide, whereas addition of triethylamine, pyridine, or NaHCO
3 led to vinylic substitution.
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Tsutomu Yokozawa, Naoro Ito, Takeshi Endo
1988 Volume 17 Issue 12 Pages
1955-1958
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Radical homopolymerization of phenylallene (PA) and copolymerization of PA with some vinyl monomers were described. PA polymerized selectively by the terminal double bond of allene both in the homopolymerization and the copolymerization. The radical reaction of PA with thiophenol was also carried out as a model reaction of the polymerization to discuss the polymerization process of PA.
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Masakatsu Hato
1988 Volume 17 Issue 12 Pages
1959-1962
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Electrically induced wettability change of polyaniline has been addressed by a potential controlled tensiometric method. Contact angle decreases with a change in the electrical potential toward more positive values. Wettability of polyaniline can be modulated by external electrical signals.
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Hitoshi Yamamoto, Hajime Yasuda, Kiyohiko Yokota, Akira Nakamura, Yasu ...
1988 Volume 17 Issue 12 Pages
1963-1966
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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A series of novel ytterbium–organoaluminum complexes has been prepared by the reaction of YbCp
*2 (THF) (Cp
*=η-C
5Me
5) with AlR
3. The X-ray structure analysis of the triethylaluminum complex, YbCp
*2Al(C
2H
5)
3 (THF), revealed the presence of unusual Yb–(μ-C
2H
5)–Al linkage. The complex catalyzes the polymerization of ethylene, methyl methacrylate and styrene in toluene.
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Atsutaka Kunai, Koji Ishihata, Sotaro Ito, Kazuo Sasaki
1988 Volume 17 Issue 12 Pages
1967-1970
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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The catalytic oxidation of benzene in the presence of air and reducing gases has been examined. All the catalysts studied, active carbon, several forms of platinum, zeolite of Cu form, and Pd/silica, were found to be effective for reducing Cu(II) to Cu(I) and thereby producing phenols. Among these, Pd/silica showed the best performance and is capable for practical use.
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Noboru Yoshida, Hiroyuki Monzen, Masatoshi Fujimoto
1988 Volume 17 Issue 12 Pages
1971-1974
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Presence of an intermediate inclusion species is demonstrated by 270 MHz
1H-NMR spectroscopy in the system of the title azo compound and the charged derivatives of α-cyclodextrin. The
1H-NMR peaks due to the sulfanilate moiety of the guest molecule are distinctly split into two peaks upon binding to the positively charged cyclodextrin, suggesting the formation of an intermediate species.
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Jadwiga Bogusiak, Wieslaw Szeja
1988 Volume 17 Issue 12 Pages
1975-1976
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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2-Benzothiazole derivatives of thiosugars can be conveniently prepared by treatment of reducing monosaccharides with tosyl chloride and 2-mercaptobenzothiazole under phase-transfer conditions.
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Sigeru Torii, Hiroshi Okumoto, Taro Kiyoto, Shigeki Hikasa
1988 Volume 17 Issue 12 Pages
1977-1978
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Electrolysis of a mixture of paraformaldehyde and terminal acetylene derivatives smoothly provided the corresponding hydroxymethylated compounds in high yields by passing less than 1 F/mol of electricity. Electroreduction of paraformaldehyde generated in situ an efficient base (EG base), which catalyzed hydroxymethylation of the acetylenes.
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Youichi Shimizu, Kenichi Uemura, Norio Miura, Noboru Yamazoe
1988 Volume 17 Issue 12 Pages
1979-1982
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Oxygen reduction performances of gas-diffusion type carbon electrodes loaded with perovskite-type oxides La
1−xCa
xMO
3 (M=Co,Mn) were examined in 30 wt% KOH at 25 °C. The highest electrode performance, i.e., 2600 mA/cm
2 at −125 mV vs. Hg/HgO, was obtained with large surface area La
0.6Ca
0.4CoO
3 prepared by an amorphous precursor method.
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Shunichi Fukuzumi, Seiji Mochizuki, Toshio Tanaka
1988 Volume 17 Issue 12 Pages
1983-1986
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Photoreduction of phenacyl halides by an NADH model compound, 10-methylacridan (AcrH
2), in MeCN proceeds via photoinduced electron transfer from the singlet excited state of AcrH
2 to phenacyl halides without the contribution of radical chain reactions, while the photoreduction by another NADH model compound, 1-benzyl-1,4-dihydronicotinamide (BNAH), proceeds via photoinduced radical chain reactions. The origin of the mechanistic difference between AcrH
2 and BNAH has been discussed.
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Toshio Kubota, Teruhiko Ishii, Hidenori Minamikawa, Sadanori Yamaguchi ...
1988 Volume 17 Issue 12 Pages
1987-1990
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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The Kolbe electrolysis of 4,4,4-trifluoro-3,3-dimethoxybutyric acid (TDBA) gave corresponding homo-coupling product, 1,1,1,6,6,6-hexafluoro-2,2,4,4-tetramethoxyhexane, which could be converted to the diene by treating with TiCl
4 followed by dehydrochlorination. Furthermore, the crossed Kolbe product from TDBA and 3-hydroxy-2-trifluoromethylpropionic acid was converted to tetrahydrofurans and an 1-olefine.
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Fey-long Wang, Wataru Ueda, Yutaka Morikawa, Tsuneo Ikawa
1988 Volume 17 Issue 12 Pages
1991-1992
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Methyl vinyl ketone was obtained at 30–40% selectivity by the reaction of methanol and acetone at 350 °C over Ti(IV)-, Cr(III)-, Mn(II)-, and Sn(IV)-exchanged forms of fluoro tetrasilicic mica (TSM). The addition of oxygen into the feed increased the conversion of acetone and the reaction over Ti(IV)-TSM converted 11% of acetone fed into methyl vinyl ketone at 85% selectivity.
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Teiji Kato
1988 Volume 17 Issue 12 Pages
1993-1996
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Overturn of molecules during the compulsory Z-type deposition using double gates was investigated by in-situ photopolymerization of a film material and by contact angle measurements of resultant LB films with water. The experimental results made inferable that molecules should overturn three times in total for every two cycles of the compulsory Z-type deposition.
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Koji Mori, Fumio Toda
1988 Volume 17 Issue 12 Pages
1997-2000
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Some alkyl aryl and dialkyl sulfoximines were resolved efficiently by complex formation with optically active 2,2′-dihydroxy-1,1′-binaphthyl and 1,6-di(
o-chlorophenyl)-1,6-diphenylhexa-2,4-diyne-1,6-diol, respectively.
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Chung-gi Shin, Nobuyuki Takahashi, Yasuchika Yonezawa
1988 Volume 17 Issue 12 Pages
2001-2002
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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It was found that the selective ester hydrolysis of
N-benzyloxycarbonyl-α-dehydroglutamic acid dimethyl ester [Cbz-ΔGlu (OMe)-OMe] with papain at pH 8.0 was achieved readily to give only a Cbz-ΔGlu(OMe)-OH almost quantitatively.
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Sadao Tsuboi, Satoshi Takatsuka, Masanori Utaka
1988 Volume 17 Issue 12 Pages
2003-2004
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Reaction of ethyl 2,3-butadienoate with aldehydes in the presence of DABCO gave ethyl 2-(1-hydroxyalkyl)-2,3-butadienoate (
2) in 41–54% yields. The reaction in the presence of butyl lithium gave
2 in 36–60% yields accompanied by ethyl 2,4-di(1-hydroxyalkyl)-2,3-butadienoate.
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Yasuaki Okamoto, Hiroshige Kane, Toshinobu Imanaka
1988 Volume 17 Issue 12 Pages
2005-2008
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Molybdenum carbonyls encaged in a NaY zeolite were found to form stable butadiene complexes; Mo(CO)
4(C
4H
6) and Mo(CO)
2(C
4H
6)
n (n = 1 or 2). These complexes are implied to deactivate the hydrogenation of C
4H
6 over molybdenum carbonyls/zeolite catalysts. The active species is proposed to be Mo(CO)
3 ads.
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Katsuhiko Inomata, Takaki Hirata, Hiroshi Suhara, Hideki Kinoshita, Hi ...
1988 Volume 17 Issue 12 Pages
2009-2012
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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The relative degree of “syn-effect” for the γ-substituted vinylsulfones in their conversion to the corresponding allylsulfones with 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) was determined by observing
E/
Z ratios of the resulting allylsulfones as follows: CH
3O– ≥ AcO– > CH
3– > –CH
2– >>
t-Bu– and Ph–.
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Hiroki Kondo, Hiroto Tanamachi, Junzo Sunamoto
1988 Volume 17 Issue 12 Pages
2013-2016
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
JOURNAL
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Phenylglycine undergoes transamination with 2-oxoglutaric acid in the presence of
N-dodecylpyridoxal chloride (DPL) and hexadecyltrimethylammonium chloride (CTACl) under mild conditions. This is the first example of nonenzymatic overall transamination realized in the absence of metal ions.
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Masato Yoshida, Hideki Mochizuki, Nobumasa Kamigata
1988 Volume 17 Issue 12 Pages
2017-2020
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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A novel type of positive halogens, sulfonyl hypochlorite or sulfonyl hypobromite was formed in the reactions of halide anions with nitrobenzenesulfonyl peroxides; these hypohalites could be used as effective reagents for halogenation of aromatic rings.
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Takuji Ogawa, Toshihiro Murafuji, Kazuhiko Iwata, Hitomi Suzuki
1988 Volume 17 Issue 12 Pages
2021-2024
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Methyl diarylbismuthinates, a new class of organic pentavalent bismuth compounds, were prepared by the reaction of triarylbismuthines with chloramine-T in methanol and their chemical properties were investigated. These compounds possess a mild and selective oxidizing ability.
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Hidetoshi Kita, Shigeaki Sasaki, Kazuhiro Tanaka, Ken-ichi Okamoto, Ma ...
1988 Volume 17 Issue 12 Pages
2025-2028
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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The use of water-permeable membranes for pervaporation in the esterification of carboxylic acid with ethanol was studied. The perfect conversion due to the equilibrium shift was obtained by using an asymmetric polyetherimide membrane for removal of water generated by the esterification.
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Koichi Komatsu, Yasuhisa Jinbu, Gregory R. Gillette, Robert West
1988 Volume 17 Issue 12 Pages
2029-2032
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Trimerization of 2,3-dibromobicyclo[2.2.2]oct-2-ene by the use of butyllithium followed by subsequent cyclization gives 1,2:3,4:5,6-tris(bicyclo[2.2.2]oct-2-eno)benzene (
3), the highly symmetrical structure of which is established by X-ray crystallography. Compound
3 is reversibly oxidized upon cyclic voltammetry at 1.25 V vs Ag/Ag
+ in CH
3CN.
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Koji Tanaka, Hajime Miyamoto, Toshio Tanaka
1988 Volume 17 Issue 12 Pages
2033-2036
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Electrochemical carboxylation of PhCOCH
3 and C
6H
10(O) coupled with CO
2 reduction by [Ru(bpy)
2(CO)
2]
2+ was carried out in CO
2−saturated dry CH
3CN. CO
2 ligated on the ruthenium atom is reduced to HCOO
− or CO upon the electrochemical reduction of the complex, where PhCOCH
3 and C
6H
10(O) function as a proton source, and the resultant carbanions react with CO
2 to afford the corresponding ketoacids, catalytically.
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Tadashi Endo, Takashi Suzuki, Yutaka Nakajima, Yutaka Sakiyama, Kunihi ...
1988 Volume 17 Issue 12 Pages
2037-2040
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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In oxidation of a pair of associating thiols, each having a phenyl or a given group (R), it has been found that the order of the selectivity agrees with that of the strength of specific R–Ph interactions for each of two sets of R [(i)
p-MeC
6H
4 < Ph <
p-MeOC
6H
4 and (ii)
n-C
5H
11 < Ph <
p-MeCOC
6H
4].
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Seiichi Takano, Youichi Shimazaki, Yoshinori Sekiguchi, Kunio Ogasawar ...
1988 Volume 17 Issue 12 Pages
2041-2044
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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A concise enantioselective synthesis of C
27−34 fragment of mycoticin B and C
31−37 fragment of amphotericin B is described using a common building block prepared from (
S)-
O-benzylglycidol.
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Kazuo Torii, Takashi Iwasaki
1988 Volume 17 Issue 12 Pages
2045-2048
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Novel Ni-hectorite inorganic complexes were synthesized hydrothermally from homogeneous Ni–Si hydrous oxide gel at 200 °C for 2 h. Dispersed slurries of these complexes showed rheological properties similar to those of natural smectites and, on heating, formed porous materials characterized by large specific surface areas and high thermal stability.
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Makoto Minato, Jiro Tsuji
1988 Volume 17 Issue 12 Pages
2049-2052
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Aldehydes are allylated efficiently by the catalysis of BiCl
3 in a two-phase electroreductive system.
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Seigo Makida, Hiroyuki Nasu, Aiko Miyamoto, Takeshi Imura, Yukio Osaka ...
1988 Volume 17 Issue 12 Pages
2053-2054
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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High-Tc superconducting Bi–Sr–Ca–Cu–O films were prepared on some metal substrates by pyrolysis of 2-ethylhexanoates. Although a high-Tc superconducting phase could seen for the films on stainless steel or silver substrates, only the films on silver substrates showed diamagnetism below 73 K and Tc(end)=68 K.
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Touru Tsukahara, Hiroyuki Kawano, Youichi Ishii, Tamotsu Takahashi, Ma ...
1988 Volume 17 Issue 12 Pages
2055-2058
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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A five-coordinate ruthenium complex with the chiral bisphosphine, (
R)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP), [RuH(BINAP)
2]PF
6 (
1) was prepared. The complex
1 was found to be a mixture of two isomers in solution. The exposure of
1 to hydrogen gas gave a chiral molecular hydrogen complex,
trans-[RuH(η
2-H
2)(BINAP)
2]PF
6 (
2). [RuD(η
2-HD)(BINAP)
2]
+ ion formed by introducing D
2 gas into a THF-d
8 solution of
1 has a H-D coupling constant
J(H,D) = 30 Hz (1:1:1), diagnostic of η
2-HD complex.
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Motoo Tori, Takeshi Hasebe, Yoshinori Asakawa
1988 Volume 17 Issue 12 Pages
2059-2060
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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(±)-Chiloscyphone, a sesquiterpene ketone isolated from the liverwort, has been synthesized starting from 3,4-dimethyl-2-cyclohexen-1-one
via intramolecular aldol condensation.
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Teruo Hinoue, Satoshi Kawada, Mitsuhiro Murata, Yu Yokoyama
1988 Volume 17 Issue 12 Pages
2061-2064
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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Temperature change of a sample solution due to optical absorption was detected by a pyroelectric sensor. A calibration curve was linear at the low concentrations of dye and the detection limit was 0.0035 cm
−1. From a solvent dependence of the signal magnitude, the signal generation could be explained by thermal conduction.
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Kazuhiko Mizuno, Toshiyuki Tamai, Isao Nakanishi, Nobuyuki Ichinose, Y ...
1988 Volume 17 Issue 12 Pages
2065-2068
Published: December 05, 1988
Released on J-STAGE: March 27, 2006
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The photoreactions of 9,10-dicyanoanthracene and 9-cyanoanthracene in the presence of biphenyl in acetcnitrile under oxygen atmosphere gave anthraquinone and 9(10
H)anthracenone, respectively, via the reaction of the radical anions of cyanoanthracenes with molecular dioxygen.
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