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Seishi Yajima, Kiyohito Okamura, Josaburo Hayashi
1975 Volume 4 Issue 12 Pages
1209-1212
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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The starting material of a continuous silicon carbide fiber with very high tensile strength is a polycarbosilane. It begins to decompose from 300°C in vacuum and is gradually converted into a β-silicon carbide fiber by the heat-treatment at the temperature above 800°C.
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Isao Mochida, Yoshimasa Ikeda, Hiroshi Fujitsu, Kenjiro Takeshita
1975 Volume 4 Issue 12 Pages
1213-1214
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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It was found that propylene was catalytically converted into acetylene and butadiene accompanied with the foramtion of coke at 150°–250° over ion-exchanged zeolites, although the yield and the catalyst life were insufficient. The activity of the ion is found in the order of Ca>Zn>Mn>H>Ni>Ag>Co>Fe>Cu. The catalytic activity may be related with the Lewis acidity.
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Tatsuaki Yashima, Osamu Iwase, Nobuyoshi Hara
1975 Volume 4 Issue 12 Pages
1215-1218
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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It was found that the shape-selective disproportionation of xylene effectively proceeded over the partially exchanged H-mordenite catalyst by the cations with a suitable ionic radius(ca. 0.07nm), and produced 1,2,4-trimethylbenzene in a high selectivity(84%).
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Kazuhiro Maruyama, Tatsuaki Iwai, Yoshinori Naruta
1975 Volume 4 Issue 12 Pages
1219-1222
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Photocycioaddition of 9,10-phenanthraquinone(PQ) and cyclic olefins; cyclohexene(
1a), cycloheptene(
1b),
cis-cyclooctene(
1c), and bicyclo[2.2.1]hept-2-ene(
2) was investigated. It was found that the product distributions and the modes of photocycloaddition were profoundly dependent on the structure of cyclic olefins.
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Hideomi Koinuma, Yasuhiko Yoshida, Hidefumi Hirai
1975 Volume 4 Issue 12 Pages
1223-1226
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Chlorocarbonylbis(triphenylphosphine)rhodium was obtained by the reaction of tris(triphenylphosphine)chlororhodium with carbon dioxide and hydrogen. Use of a polar aprotic solvent was effective for the reaction. This reaction indicates carbon dioxide is reduced by molecular hydrogen on a rhodium complex and fixed in the form of a carbonyl complex.
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Seishi Yajima, Kiyohito Okamura, Toetsu Shishido
1975 Volume 4 Issue 12 Pages
1227-1230
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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By rapid quenching of the melt, an amorphous phase of yttrium-cobalt-boron system was obtained. The phase is stable at room temperature, and its crystallization takes place in the vicinity of 700°C on heating at 10°C/min. Electrical resistivity of the amorphous phase is constant at about 10
−3Ωcm in the temperature range below 660°C; the variation in the resistivity with the transition from the amorphous to the equilibrium state was measured.
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Shunichi Kawamura, Akeshi Sato, Takeshige Nakabayashi, Masayuki Hamada
1975 Volume 4 Issue 12 Pages
1231-1234
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Acetyl benzyl and acetyl benzhydryl disulfides which were labeled with
35S at acetylsulfenyl sulfur, were prepared, and were allowed to react with triphenylphosphine. Radioassay of triphenylphosphine sulfide obtained showed that the benzylsulfenyl sulfur atom of the former, and, on the contrary, acetylsulfenyl sulfur in the latter compound was extruded.
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Shigeo Nishimura, Mamoru Katagiri, Yuzo Kunikata
1975 Volume 4 Issue 12 Pages
1235-1240
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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2- and 4-Methoxycyclohexanones give the alcohols of higher cis/trans ratios than the corresponding methylcyclohexanones in the catalytic hydrogenation over platinum metals. This trend is most clearly seen over iridium and platinum among the six platinum metals. Hydrogenation with platinum gives the alcohols of higher cis/trans ratios in
t-butyl alcohol than in other solvents.
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Hiroo Inoue, Hiroyuki Hata, Eiji Imoto
1975 Volume 4 Issue 12 Pages
1241-1244
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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It is found that α-halo ketones are reduced with benzenethiol in the presence of iron-polyphthalocyanine to the parent ketones, although they are not reduced in the absence of iron-polyphthalocyanine. The iron-polyphthalocyanine appears to serve as an electron-transfer catalyst for the reductive dehalogenation.
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Hironori Arakawa, Atsumu Ozaki
1975 Volume 4 Issue 12 Pages
1245-1248
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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The molybdic anhydride-catalyzed epoxidation of olefin by
t-butyl hydroperoxide was studied with particular reference to the induction period and the effect of additives. The epoxidation in the presence of hexamethylphosphorictriamide(HMPT) proceeds through an intermediate complex, MoO(O
2)
2-HMPT, which was isolated as an adduct with bipyridyl.
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Michiro Hayashi, Misako Imachi
1975 Volume 4 Issue 12 Pages
1249-1252
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Microwave spectra of dimethylether and its deuterated species, (CD
3)
2O, in the excited torsional states were studied in relation to the top–top coupling problem of internal rotation of two methyl groups. A preliminary analysis of the observed splittings of the spectra was carried out in order to evaluate V
3, V′ and V″ values in the potential function.
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Michio Kobayashi, Tamio Sakai, Hiroshi Minato
1975 Volume 4 Issue 12 Pages
1253-1256
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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In hexamethylphophoramide,
18O-labelled nitrite ion readily exchanged with the nitro group of p-dinitrobenzene at 30°C, whereas the formation of
p-nitrophenol by the O-attack of nitrite ion is much slower.
p-Nitrochlorobenzene is quickly converted to
p-dinitrobenzene by the N-attack of nitrite ion, and
p-nitrophenol is the final product. The nitro group of
p-nitrobenzonitrile is slowly exchanged with nitrite ion.
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Fred G. Schreiber, Robert Stevenson
1975 Volume 4 Issue 12 Pages
1257-1258
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Short procedures for the synthesis of the lignans (egonol,
homo-egonol and the title compound) which are constituents of various Styrax species are reported.
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Yoshinao Oosawa, Taro Saito, Yukiyoshi Sasaki
1975 Volume 4 Issue 12 Pages
1259-1260
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Several bidentate phosphorus ylide ligands of the type Ph
2P–(CH
2)
n–P
+(Ph
2)–C
−H–C(O)–R (n = 1, R = Ph; n = 2, R = CH
3, OCH
3) and their complexes of palladium(II) and platinum(II) chlorides have been synthesized and characterized.
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Tsutomu Nonaka, Akio Udagawa, Keijiro Odo
1975 Volume 4 Issue 12 Pages
1261-1266
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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The electrolytic reductions of some aromatic diketones were carried out by means of controlled potential electrolysis in various catholytes. Reduction products were intramolecular pinacols (
cis and
trans cyclic vicinal diols), intermolecular pinacol, and/or hydrol. The formation ratios of the products were strongly dependent on the molecular structure of diketone, the pH of catholyte, and/or the kind of organic co-solvent.
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Michiro Hayashi, Jun Nakagawa, Kazunori Kuwada
1975 Volume 4 Issue 12 Pages
1267-1270
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Microwave spectra of
gauche-ethanethiol were studied in relation to its molecular structure. The r
s structure of this molecule could be determined and was compared with that of trans isomer. Discussions were made on the angles around the carbon atom of the CH
2 group in the molecule.
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Israel Agranat, Mordecai Rabinovitz, Henry Selig, Chun-Hsu Lin
1975 Volume 4 Issue 12 Pages
1271-1272
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Phenanthrene reacts with xenon difluoride without HF initiation and in an open system to give fluorine substitution and addition products; 9-fluorophenanthrene is isolated in 33% yield.
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Arie Dagan, Guan-Su Shaw, Aviv Gazit, Mordecai Rabinovitz
1975 Volume 4 Issue 12 Pages
1273-1276
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Two geometrical isomers of 4,5:8,9-dibenzo-2,10-cycloundecadien-6-yne were prepared by a Wittig reaction between 2,2′-diformyldiphenylacetylene and trimethylenedi(triphenylphosphonium bromide). Their stereochemical configuration,
cis,
trans (
I) and
trans,
trans (
II) were deduced from the nmr spectral data. Attempts to use (
I) and (
II) as precursors to the [11]annulenyl cation (
III) have so far not been realized.
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Michinori Oki, Waro Nakanishi, Michio Fukunaga, G. David Smith, Willia ...
1975 Volume 4 Issue 12 Pages
1277-1280
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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2,2-Dimethyl-1-phenylthiiranium hexachloroantimonate was prepared in sulfur dioxide. The direction of ring-opening of the thiiranium ion was found to differ according to the reaction conditions. The structures of the products were determined by independent synthesis and by X-ray crystallography.
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Shinichi Tsuji, Shoichi Kusumoto, Tetsuo Shiba
1975 Volume 4 Issue 12 Pages
1281-1284
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Enduracididine (
1), a component amino acid of the antibiotic enduracidin, was synthesized starting from
L-histidine. Bamberger cleavage of methyl
L-histidinate followed by catalytic hydrogenation afforded a mixture of (2
S,4
R)- and (2
S,4
S)-2,4,5-triaminopentanoic acid derivatives. Deprotection and guanidination of them yielded
1 of the natural configuration and its diastereoisomer, i.e., the enantiomer of natural alloenduracididine respectively.
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Kenshô Sagisawa, Hideko Kiriyama, Ryôiti Kiriyama
1975 Volume 4 Issue 12 Pages
1285-1288
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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The spin-lattice relaxation times of
1H and
35Cl as well as the
35Cl NQR frequencies in α-NH
4HgCl
3 are reported. The proton
T1 data are explained in terms of C
3 reorientation and S
4 flip of NH
4+ ions. The latter mode is also largely responsible for the
35Cl quadrupole relaxation rate. A marked change in the proton
T1 at 55 K indicates a phase transition, ascribable to the ordering of the NH
4+ ions.
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Takatoshi Narisawa, Mizuka Sano, Yasumasa J. I’haya
1975 Volume 4 Issue 12 Pages
1289-1292
Published: December 05, 1975
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The lowest energy absorption peak was found at 22154.0 cm
−1 for a thick single crystal of 9,10-anthraquinone at 4.2 K. From the analysis of Zeeman absorption patterns for the intense, sharp peaks observed at 22319.3 and 22357.9 cm
−1, the lowest triplet state was assigned to
3B
1g.
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Yasushi Inoue, Yoshimune Yamada
1975 Volume 4 Issue 12 Pages
1293-1294
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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The isotopic exchange rate of sodium ion between crystalline zirconium phosphate and molten NaNO
3 has been measured at 312°C and 362°C by batch method. The equilibrium was reached within 20 minutes at either temperature, and the rate was very rapid as compared with that of sodium-potassium ion exchange.
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Miki Niwa, Makoto Mizutani, Yuichi Murakami
1975 Volume 4 Issue 12 Pages
1295-1298
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Oxidation of methanol into formaldehyde on SnO
2–MoO
3 catalyst proceeds according to the redox mechanism of Mo
+5\
ightleftharpoonsMo
+4.
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Yuki Fujii, Takashi Isago, Mitsuo Sano
1975 Volume 4 Issue 12 Pages
1299-1302
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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A new mixed cobalt(III) complex containing 7,7′-Me-sal
2en and
L-proline,
cis-β-[Co(7,7′-Me-sal
2en)(
L-pro)], has been prepared from [Co(7,7′-Me-sal
2en)] and
L-proline in methanol (80%) by air oxidation. The reaction has proceeded stereoselectively to form (−)
435-isomer, followed by slow isomerization to form finally (+)
435-isomer (100%).
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Kimio Kunimori, Tomoji Kawai, Tamotsu Kondow, Takaharu Onishi, Kenzi T ...
1975 Volume 4 Issue 12 Pages
1303-1304
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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High resolution Auger spectra indicate that NO is dissociatively adsorbed on a polycrystalline tungsten surface at room temperature.
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Keiichi Kawano, Yoshimasa Kyogoku
1975 Volume 4 Issue 12 Pages
1305-1308
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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Natural abundance
15N nmr spectra of L-histidine, and τ- and π-methylhistidines were measured. The signal assignments to the τ- and π-nitrogen could be made by comparison of these spectra. From the pH titration of the
15N chemical shifts, it is directly proved that the τ-H tautomer is predominant in a basic solution.
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Noriyuki Sotani, Masatomo Hasegawa
1975 Volume 4 Issue 12 Pages
1309-1312
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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The needles appeared at the end of the crystal of molybdenum oxide used as a catalyst for hydrodesulfurization for 10 min at 350°C. They gradually grew and apparently stopped to grow after the 40 min reaction. The needles were produced in the presence of thiophene. They gave the ED pattern due to MoO
2. Also the catalyst was sulfurized uniformly all over the surface.
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Hajime Matsushita, Masao Noguchi, Sadao Yoshikawa
1975 Volume 4 Issue 12 Pages
1313-1316
Published: December 05, 1975
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The optical activation of racemic α-substituted carbonyl compounds by the hydrolysis of enamines with optically active α-pipecoline was reported. Solvent effect on the optical activation was also examined.
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Yoshinobu Inouye, Yuji Uchida, Hiroshi Kakisawa
1975 Volume 4 Issue 12 Pages
1317-1318
Published: December 05, 1975
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It is established that cacalol is 5,6,7,8-tetrahydro-3,4,5-trimethylnaphtho[2,3-b]furan-9-ol by synthesis in several steps from creosol methyl ether.
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Jyuzo Nakayama, Mimiko Imura, Masamatsu Hoshino
1975 Volume 4 Issue 12 Pages
1319-1320
Published: December 05, 1975
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A new reagent, 2-(3-methylbutoxy)-1,3-benzodithiole, could be used to introduce a cyclic dithioacetal function into 2- or 3-position of indoles and pyrroles in almost quantitative yields under mild conditions.
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Shigeo Tazuke, Kaname Sato, Fumio Banba
1975 Volume 4 Issue 12 Pages
1321-1324
Published: December 05, 1975
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Fluorescence of various polyesters prepared from 2-(9-anthryl)methylpropane-1,3-diol was quenched by various polyesters prepared from 2-(4-dimethylaminobenzyl)propane-1,3-diol. The sequence of quenching constants(K
q) was discussed with special reference to the polymer structures of fluorescers and quenchers. When terephthalate groups were incorporated in the main chain of quencher, K
q increased very much, which was interpreted by cooperative quenching action of donor(amine) and acceptor(terephthalate). This concept was unequivocally evidenced by separate experiments.
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Masao Hashimoto
1975 Volume 4 Issue 12 Pages
1325-1329
Published: December 05, 1975
Released on J-STAGE: March 27, 2006
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The
35Cl NQR frequencies of magnesium trichloroacetate hexahydrate, sodium trichloroacetate trihydrate, and anhydrous sodium trichloroacetate were measured in the temperature region of 77–230 K. It was found that each of the two hydrated salts contains two thermally different non-equivalent trichloromethyl groups. The non-equivalence may be due to some intermolecular interaction.
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Akira Arase, Yuzuru Masuda
1975 Volume 4 Issue 12 Pages
1331-1332
Published: December 05, 1975
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Alkylmagnesium halides and alkyllithiums reacted with selenium dioxide, suspended in tetrahydrofuran, to afford dialkyl selenides in 30–62 % yields.
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Shuji Teratake, Shun-ichi Morikawa
1975 Volume 4 Issue 12 Pages
1333-1336
Published: December 05, 1975
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Reactions of 2-lithio-3-(tri-
n-butylstannyl)propionitrile (
1) with alkyl halides or carbonyl compounds gave the corresponding 2-substituted 3-(tri-
n-butylstannyl)propionitriles (
2), which were reduced to amines (
4) and then diazotized to give alkyl cyclopropanes or cyclopropanemethanols, respectively, in moderate overall yields.
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