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Tatsuo Arai, Hirochika Sakuragi, Katsumi Tokumaru
1980 Volume 9 Issue 11 Pages
1335-1338
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Photostationary state compositions and quantum yields were determined for triplet sensitized isomerization of 3,3-dimethyl-1-(2-naphthyl)-1-butene in benzene. The ratio of the trans isomer at the photostationary state increased with increasing concentration of oxygen, which, combined with the azulene effect, indicates that both of transoid and twisted triplets are quenched by oxygen.
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Tadashi Suehiro, Takaaki Tashiro, Ryuichi Nakausa
1980 Volume 9 Issue 11 Pages
1339-1342
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Esr spectra of phenyl- and p-substituted phenyl-diazenyl radicals in solution give a
N1 \backsimeq 23 G, a
N2 - 9.4 G, and a
H \backsimeq 1.1 G (two meta hydrogens), suggesting a free rotation of the N
1=N
2 group around the C
1–N
1 bond. o-Monosubstituted phenyldiazenyl radicals prefer to take a planar conformation, and show a hyperfine coupling constant of only one meta hydrogen-5.
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Satoru Onaka, Yoshinori Kondo, Nobuhiro Furuichi, Koshio Toriumi
1980 Volume 9 Issue 11 Pages
1343-1346
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Photochemical reactions of the title compounds afforded an air-stable colorless crystalline compound in low yield. The product was characterized as an orthometalated manganese triphenylphosphite derivative by elemental analyses and an X-ray diffraction technique. Its crystal structure is described.
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Toyoki Kunitake, Naotoshi Nakashima, Kozo Morimitsu
1980 Volume 9 Issue 11 Pages
1347-1350
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Chiral, single-chain ammonium amphiphiles which possess the alanine unit formed disk-shaped bilayer aggregates in water. Circular dichroism of the chiral aggregate was much enhanced at temperatures below the phase transition.
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Hisatoshi Konishi, Yuji Kasamatsu, Satoru Nanjo, Tamon Okano, Jitsuo K ...
1980 Volume 9 Issue 11 Pages
1351-1354
Published: November 05, 1980
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Nitrobenzene was deoxygenated by carbon to give azobenzene. Impregnation of K
2CO
3 on the carbon markedly lowered the temperature required for the reaction. The catalytic activity of K
2CO
3 was correlated to the oxidation behavior of the carbon observed by TGA and DTA in air.
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Noboru Yamazaki, Seiichi Nakahama, Kazuo Yamaguchi, Tetsuhiko Yamaguch ...
1980 Volume 9 Issue 11 Pages
1355-1358
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Sulfur dichloride was allowed to react with linear and cyclic, silyl and tin sulfides prepared from alkanedithiols. Of the sulfides, bis(trimethylsilyl) sulfides were most effective for synthesis of cyclic trisulfides.
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Yonezo Maeda, Hiroki Ohshio, Yoshimasa Takashima
1980 Volume 9 Issue 11 Pages
1359-1362
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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The
57Fe Mössbauer emission spectroscopic technique has been applied to the study of after-effects of electron capture in [
57Co(terpy)
2]Cl
2·5H
2O and [
57Co(terpy)
2] (ClO
4)
2·2H
2O (where terpy= 2,2′,2″-tripyridyl) which exhibit an anomalous magnetic behavior. These results were interpreted on the basis of the difference in the spin multiplicity of the central cobalt ion.
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Hitomi Suzuki, Hisako Abe, Atsuhiro Osuka
1980 Volume 9 Issue 11 Pages
1363-1364
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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In hexamethylphosphoric triamide containing copper (I) iodide, nonactivated aryl iodides undergo a facile nucleophilic attack by arenethiolate ions to give the corresponding aryl sulfides in good yields.
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Noboru Ono, Hideyoshi Miyake, Yo Tanabe, Kazuhiko Tanaka, Aritsune Kaj ...
1980 Volume 9 Issue 11 Pages
1365-1368
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Allylation sulfur substituted active methylene compounds such as RSCH
2Y [Y = C(=O)R, COOR, CN] with allylic bromides in the presence of bases gives a mixture of the S
N2-product and the apparent S
N2′-product. The former product is selectively obtained in alkylation in a nonpolar solvent. Synthetic utility of this regiospecific allylation is demonstrated in the simple synthesis of pellitorine.
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Otohiko Tsuge, Hidehiko Shiraishi, Toshiaki Takata
1980 Volume 9 Issue 11 Pages
1369-1372
Published: November 05, 1980
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1,3-Diphenylthiazolo[3,4-
a]benzimidazole, a new 10π-electron heterocycle containing tetravalent sulfur, was prepared by the reaction of 1,2-dibenzoylbenzimidazole with phosphorus pentasulfide in refluxing toluene. Its cycloadditions with alkenes and alkynes occurred across the thiocarbonyl ylide dipole in highly stereoselective and/or regiospecific fashions.
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Masaru Inage, Haruyuki Chaki, Shoichi Kusumoto, Tetsuo Shiba, Akira Ta ...
1980 Volume 9 Issue 11 Pages
1373-1376
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Synthesis is described on 6-
O-[2-deoxy-2-((
R)-3-hydroxytetradecanoylamino)-6-
O-tetradecanoyl-β-
D-glucopyranosyl]-2-deoxy-2-((
R)-3-hydroxytetradecanoylamino)-3,4-di-
O-tetradecanoyl-
D-glucopyranose which corresponds to the phosphate-less lipid A structure of
Salmonella-type bacterial endotoxin.
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Noboru Yoshida, Masatoshi Fujimoto
1980 Volume 9 Issue 11 Pages
1377-1380
Published: November 05, 1980
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Inclusion reactions of the title compounds with α-cyclodextrin were studied in aqueous solution by means of a temperature-jump method. The rate constants for inclusion reactions were found to be in the order of magnitude 10
6–10
7 mol
−1 dm
3 s
−1.
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Mitsuo Sato, Toshihiko Ogura
1980 Volume 9 Issue 11 Pages
1381-1384
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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A new concept of coordination network is introduced for classifying and deriving possible frameworks of tectosilicates. 26 topologically different networks have been derived by connecting points with the degree of freedom 3 in the 2nd distance. 39 different tectosilicate structures are examined in view of this coordination network.
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Yuzo Yoshikawa
1980 Volume 9 Issue 11 Pages
1385-1388
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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The conformational analysis was performed for the systems of the ion pairs, Λ-[Co(en)
3]
3+–ClO
4−–, – SO
42−– , –PO
43−–, and -tart
2−- nH
2O. The analysis of the Λ-[Co(en)
3]
3+ - tart
2− - 25H
2O systems gave the results consistent with the experimental data of the stereoselective ion associations, in which the approximation of a dielectric constant dependent on inter-charge distance was made. The structures of Λ-[Co(en)
3]
3+ -tart
2− suggest that two hydroxyl groups of a tartrate ion play an important role.
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Kyosuke Satake, Masaru Kimura, Shiro Morosawa
1980 Volume 9 Issue 11 Pages
1389-1390
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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6,7-Dihydroazirino[1 ,2-
a]thieno[2,3-
d]pyridin-8-one
7 was synthesized and its base-catalyzed ring-opening leading to 4,5-dihydro-8
H-thieno[3,2-
c]azepin-8-one
8 was studied.
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Hiroshi Kasai, Ziro Yamaizumi, Keiji Wakabayashi, Minako Nagao, Takash ...
1980 Volume 9 Issue 11 Pages
1391-1394
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Structure of a mutagenic compound (Me-IQ) isolated from broiled fish was determined to be 2-amino-3,4-dimethylimidazo[4,5-
f]quinoline based on the mass-, UV- and
1H-NMR-spectra and chemical synthesis. Me-IQ showed strong mutagenic activity towards
Salmonella typhimurium TA98 in the presence of S-9 mix.
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Ken’ichi Takeuchi, Takamasa Moriyama, Tomomi Kinoshita, Hitoshi ...
1980 Volume 9 Issue 11 Pages
1395-1398
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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1-Adamantyl trifluoromethanesulfonate (
1) has been prepared from 1-bromoadamantane and silver trifluoromethanesulfonate in 2,2-dimethylbutane. The trifluoromethanesulfonate (
1) abstracts hydride from pentane or hexane to form adamantane, initiates ring-opening polymerization of tetrahydrofuran, and reacts with alkyllithiums to afford 1-alkyladamantanes.
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Keiji Iriyama, Fumio Mizutani, Masahiko Yoshiura
1980 Volume 9 Issue 11 Pages
1399-1402
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Remarkable absorption spectral change and enhancement of photocurrent due to chromophore aggregation have been achieved by treating a cast film of a new surface-active and photo-active merocyanine dye on an optically transparent SnO
2 electrode with an alkaline aqueous solution.
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Toru Koizumi, Hiroyasu Takagi, Eiichi Yoshii
1980 Volume 9 Issue 11 Pages
1403-1406
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Diastereomerically pure ethyl
N-[chloro(phenyl)thiophosphonyl]-
L-prolinate was prepared. From this intermediate various optically active phenylphosphonic acid derivatives have been obtained in high optical yields. Their absolute configurations have been determined by the chemical correlation.
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Yoshinobu Inouye, Junko Hara, Hiroshi Kakisawa
1980 Volume 9 Issue 11 Pages
1407-1410
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Four
N-alkyl-α-alkoxycarbonylnitrones were prepared and their NMR spectra in C
6D
6, CDCl
3, or CD
3SOCD
3 were measured. From the analyses of the spectra, it was found that the nitrones exhibited a facile equilibrium in all solvents used and
E/
Z ratio in equilibrium depended largely on the polarity of the solvent.
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Sotaro Ito, Toshimasa Yamamoto, Yuji Tokushige
1980 Volume 9 Issue 11 Pages
1411-1414
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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The copper(II) chloride-catalyzed oxidation of
L-ascorbic acid (AA) by O
2 was found to involve both the anaerobic oxidation of AA by copper(II) chloride and the reoxidatian steps of copper(I) chloride by O
2 in the catalytic cycle, by comparing the rate of copper(II)-catalyzed oxidation of AA by O
2 (R
AIIO) with those of anaerobic oxidation of AA by copper(II) (R
AII) and oxidation of copper(I) by O
2 (R
IO).
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Koichi Narasaka, Hong Chang Pai
1980 Volume 9 Issue 11 Pages
1415-1418
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Meso(or
erythro) 1,3-diols are prepared in high stereoselectivity from β-hydroxyketones by the treatment with tributylborane and the successive reduction with sodium borohydride.
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Hiroshi Takaku, Tadaaki Nomoto, Mitsuho Murata, Tsujiaki Hata
1980 Volume 9 Issue 11 Pages
1419-1422
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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In the presence of cesium fluoride, the reactions of a fully protected 5′-
O-dimethoxytrityl-2′-
O-tetrahydropyranyl-
N-acylnucleoside 3′-(4-chlorophenyl, 5-chloro-8-quinolyl) phosphates with 5′-hydroxyl nucleosides proceeded rapidly under mild conditions to afford the corresponding ribodinucleoside monophosphates in good yields.
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Hisatoshi Konishi, Kiyoshi Yokota, Yuji Ichihashi, Tamon Okano, Jitsuo ...
1980 Volume 9 Issue 11 Pages
1423-1426
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Chlorination of alkylbenzenes was carried out with chlorine in carbon tetrachloride in the presence of chemically-modified silica catalysts. The
para/ortho ratios were remarkably higher than those obtained in the FeCl
3-catalyzed chlorination.
t-Butylbenzene was chlorinated at
para-position almost exclusively. The catalyst could be reused several times.
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Yoshikazu Sugihara, Yoshiko Fujiyama, Ichiro Murata
1980 Volume 9 Issue 11 Pages
1427-1430
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Some fulvalenoids containing 1,3-dithiepin counterpart (
5a), (
5b), and (
5c) have been synthesized through the reaction of 2-trimethylsilyl-1,3-dithiepinide ion (
6) with di-
tert-butyl-cyclopropenone, 2,3;6,7-dibenzotropone, and fluorenone, respectively. Comparison of the
1H-NMR spectra of these fulvalenes indicated the electron accepting ability of the 1,3-dithiepin moiety.
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Toshio Eiki, Mikio Mori, Shuji Kawada, Kazumi Matsushima, Waichiro Tag ...
1980 Volume 9 Issue 11 Pages
1431-1434
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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N-Dodecyl-2-hydroxymethylimidazole (
1) was found to be unusually active in the transesterification toward
p-nitrophenyl picolinate (
4), when the reaction was carried out in the presence of CTABr micelle and zinc ion.
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Isao Aso, Taro Amamoto, Noboru Yamazoe, Tetsuro Seiyama
1980 Volume 9 Issue 11 Pages
1435-1438
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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In an attempt to determine oxygen adsorption sites of the Fe
2O
3–Sb
2O
4 catalysts, SIMS measurements of the catalysts were performed after
18O
2 preadsorption (SIMS-
18O tracer method). It was clearly shown that the adsorbed oxygen was accommodated by the surface Sb ions.
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Hironobu Hashimoto, Katsuji Asano, Fumiko Fujii, Juji Yoshimura
1980 Volume 9 Issue 11 Pages
1439-1440
Published: November 05, 1980
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The structure of 6-aminoheptonic acid component contained in destomycin A and C was confirmed first by chemical synthesis.
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Toshikazu Takata, Mayumi Yamazaki, Ken Fujimori, Yong Hae Kim, Shigeru ...
1980 Volume 9 Issue 11 Pages
1441-1444
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Asymmetric induction and diastereomeric ratio in the enzymatic oxygenation of various sulfides to the corresponding sulfoxides with hepatic mirosomal cytochrome P-450 obtained from phenobarbital pretreated rabbit were investigated in comparison with those of nonenzymatic oxidation with
m-chloroperbenzoic acid and sodium metaperiodate. While substantial asymmetric inductions were observed in the sulfoxides formed by the enzymattc oxygenations, diastereomeric ratios of the sutfoxides formed were also quite different from those obtained by oxidation with
m-chloroperbenzoic acid and sodium metaperiodate.
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Mitsuyasu Kawakami, Hideaki Iwanaga, Shuichi Kagawa
1980 Volume 9 Issue 11 Pages
1445-1448
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Permeabilities for N
2, O
2, and CO
2 through cellulose nitrate/polyethylene glycol blend membranes were determined as a function of film composition. Not only the permeability but the permselectivity for CO
2 increased with an increase in the fraction of polyethylene glycol. It was suggested that the intermolecular force induced by polar groups in the film and the role of polyethylene glycol as a plasticizer may be responsible for such a behavior for CO
2.
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Shuji Oishi, Isao Tate
1980 Volume 9 Issue 11 Pages
1449-1452
Published: November 05, 1980
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RNd(WO
4)
2(R=Li,Na and K) crystals were grown from high-temperature solutions of ternary systems Nd
2O
3–WO
3–R
2CO
3 by slow cooling. Grown RNd· (WO
4)
2(R=Li and K) crystals were generally bigger than NaNd(WO
4)
2 crystals. These crystals, whose shapes were octahedron or decahedron, were reddish purple and mostly transparent. Among these tungstate crystals, NaNd(WO
4)
2 crystals had the highest melting point of 1235±5°C.
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Hiroshi Nozaki, Yoshie Fukuoka, Akihiko Matsuo, Osamu Soga, Mitsuru Na ...
1980 Volume 9 Issue 11 Pages
1453-1454
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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A new dehydro-γ-lactam, sargassumlactam, has been isolated from the brown alga
Sargassum kjellmanianum, and its structure was determined to be 4,5-dehydro-3-methoxy-3,5-dimethoxycarbonyl-2-pyrrolidone by the spectroscopic and X-ray diffraction analysis.
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Nobukatsu Katsui, Fujio Yagihashi, Akio Murai, Tadashi Masamune
1980 Volume 9 Issue 11 Pages
1455-1458
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Structure and configuration of rishitinone, a stress metabolite isolated from diseased potato tubers, was determined to be formula
1 on the basis of the chemical and spectral evidence.
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Mitsuo Takasugi, Yoshikazu Kumagai, Shigemitsu Nagao, Tadashi Masamune ...
1980 Volume 9 Issue 11 Pages
1459-1460
Published: November 05, 1980
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Two antifungal compounds, designated as broussin and broussonin C, were isolated from wounded xylem tissues of paper mulberry shoots and identified as flavan and 1,3-diphenylpropane derivatives, respectively.
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Reiji Takeda, Yoshimoto Ohta, Yoshio Hirose
1980 Volume 9 Issue 11 Pages
1461-1464
Published: November 05, 1980
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Two new sesquiterpene lactones, named (+)-β-frullanolide and (+)-brothenolide, were isolated from liverwort
Frullania brothevi Steph.
The absolute structures of these lactones have been established.
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Kiyohiko Tajima, Hiroshi Itoh, Hitoshi Morooka
1980 Volume 9 Issue 11 Pages
1465-1466
Published: November 05, 1980
Released on J-STAGE: March 27, 2006
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Triacetate of
D-glucuronolactone (
1) or
D-mannuronolactone (
2) is converted to 3-acetoxy-6-diacetoxymethylpyrane-2-one (
3) and 2,5, 6 6-tetraacetoxy-2,4-hexadienoic acid (
4) respectively by treatment with acetic anhydride-potassium acetate-18-crown-6 or acetic anhydridetriethylamine.
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