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Susumu Tajima, Takeshi Sato, Tamae Yanagisawa, Tadashige Azami, Toshik ...
1977 Volume 6 Issue 3 Pages
203-206
Published: March 05, 1977
Released on J-STAGE: March 27, 2006
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The average translational energy of ions has been readily measured by applying a variable retarding potential of negative voltage to the repeller electrode. The measured value of the methyl ion from acetonitrile at the threshold is in fair agreement with that in literature.
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Tetsuo Osa, Shigeaki Fujieda, Yasuhiko Abe, Yasukazu Ohkatsu
1977 Volume 6 Issue 3 Pages
207-210
Published: March 05, 1977
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Absorptions of an equimolar mixture of NO and NO
2 in an aqueous solution of ammonium salts and with a cation-exchange resin substituted by ammonium ion were investigated by a flow method. Ammonium salts such as phosphate, benzoate, and oxalate were found effective for the removal of nitrogen oxides. Effects of temperature and time of contact were examined.
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H. Ahlbrecht, C. Vonderheid
1977 Volume 6 Issue 3 Pages
211-214
Published: March 05, 1977
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NMR-Untersuchungen zeigen, daß die durch Phosgenierung der Amide
1 zugänglichen
N-Vinylcarbamidsäurechloride
3 als nicht planare, chirale Konformere vorliegen.
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Hisashi Ito, Masaaki Hagiwara, Iwao Ichikizaki, Kenji Takahashi
1977 Volume 6 Issue 3 Pages
215-216
Published: March 05, 1977
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A water-insoluble derivative of ribonuclease T
1 (RNase T
1) was prepared by chemically combining RNase T
1 with a copolymer of acrylamide and divinylbenzene (Enzacryl AH), and its enzymatic properties were examined. The enzyme derivative retained much of its original activity and was considerably more stable to heat and extremes of pH than the native enzyme.
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Yoshiharu Hisamatsu, Masaakira Iguchi
1977 Volume 6 Issue 3 Pages
217-220
Published: March 05, 1977
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Hydrogen uptake of a solution containing pentacyanocobaltate(II) ions was found to be inhibited by Tl(I) ions. It was confirmed by a rapid-scan spectroscopic method that pentacyanocobaltate(II) ions react with Tl(I) ions in an aqueous solution to give the dimeric complex, [(CN)
5CoTlCo(CN)
5]
5−. The dimeric complex containing Co-Tl-Co linkage was successfully isolated as a solid state.
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Michiro Hayashi, Misako Imachi, Makoto Saito
1977 Volume 6 Issue 3 Pages
221-222
Published: March 05, 1977
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Microwave spectra of allylsilane and its deuterated species were measured. Their rotational constants determined were predictable by a model having a set of structural parameters transferred from those of 1-butene and ethylsilane and the skeletal dihedral angle of 103°40′. Dipole moment obtained by Stark effect measurements was 0.526±0.022 D for the normal species making an angle of about 36° with the SiC bond. From the observed splittings of the spectra due to the excited silyl torsional state, the barrier to SiH
3 internal rotation was determined to be 2130±70 cal/mol.
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Toshio Wakabayashi, Kenzo Watanabe, Yoshinori Kato, Masahiko Saito
1977 Volume 6 Issue 3 Pages
223-228
Published: March 05, 1977
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(
S)-(+)-2-oxo-6-piperidineacetic acid was synthesized by a novel route involving an asymmetric cyclization process. Its absolute configuration was determined by converting it to (
S)-(−)-sedamine and (
S)-(−)-allosedamine, piperidine alkaloids.
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Kiyoshi Nara, Kazuyoshi Katamoto, Shigeru Suzuki, Shunichi Akiyama, Ei ...
1977 Volume 6 Issue 3 Pages
229-234
Published: March 05, 1977
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The absolute configuration of the aminopolyol moiety (XI) of the aminoglycoside antibiotics P-2563 (P) (I) and (A) (II) was established to be 2
S, 3
S, 4
R and 5
S from the evidence that XI gave methyl 3,6-diacetamido-3,6-dideoxy-α-
L-gulopyranoside through the oxidation of the hydroxymethyl group at C-6. From this fact, together with the plane structures of I and II and
13C-NMR studies, the absolute configuration of I and II were elucidated to be 3-
O-(4-deoxy-4-propionamido-α-
D-glucopyranosyl)-(2
S, 3
S, 4
R, 5S)-1,4-diamino-1,4-dideoxyhexitol and 3-
O-(4-acetamido-4-deoxy-α-
D-glucopyranosyl)-(2
S, 3
S, 4
R, 5
S)-1,4-diamino-1,4-dideoxy-hexitol, respectively.
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Akio Murai, Noriaki Iwasa, Tadashi Masamune
1977 Volume 6 Issue 3 Pages
235-236
Published: March 05, 1977
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The transformation of jervine into testosterone is described.
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Satsuki Abe
1977 Volume 6 Issue 3 Pages
237-240
Published: March 05, 1977
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Polyvinylcarbazole reacts selectively with nitrogen dioxide and develops a yellow color. The color producing components are identified to be nitro derivatives of the polymer. A new indicator tube developed as an application of this reaction will be used conveniently for the detection of nitrogen dioxide in the field of industrial hygiene.
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Hajime Takahashi, Masaaki Ito, Hiroshi Suginome
1977 Volume 6 Issue 3 Pages
241-244
Published: March 05, 1977
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A facile three-step ring contraction of sesquiterpene widdrol (
1) is described. The steps involve the first known example of the photoreaction of a 7-membered cyclic homoallyl alcohol nitrite to afford four isomeric α,β-unsaturated oximes (
3), (
4), (
5) and (
6).
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Takeshi Takeda, Masahiro Ueda, Teruaki Mukaiyama
1977 Volume 6 Issue 3 Pages
245-248
Published: March 05, 1977
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Various α-hydroxy ketones were prepared in good yields by reduction of α-ethoxycarbonylhydrazono ketones with NaBH
4, followed by acid hydrolysis. α-Ethoxycarbonylhydrazono ketones were obtained in good yields by the treatment of Δ
2-1,3,4-oxadiazolines, prepared from 1-(2-oxoalkyl)pyridinium salts and diethyl azodicarboxylate, with aqueous sodium hydroxide.
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Junzo Nokami, Norio Kunieda, Masayoshi Kinoshita
1977 Volume 6 Issue 3 Pages
249-252
Published: March 05, 1977
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The reaction of (+)-(
R)-α(p-tolylsulfinyl)acetophenone(
1) with alkyl Grignard reagents in tetrahydrofuran is described. When
1 was treated with 2 equiv of ethylmagnesium iodide in tetrahydrofuran at 0°C, (−)-ethyl
p-tolyl sulfoxide and α(ethylsulfinyl)acetophenone were obtained.
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Ikuo Saito, Kunio Sakan, Shô Itô
1977 Volume 6 Issue 3 Pages
253-256
Published: March 05, 1977
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The reaction of nitrosotropolone
1 with cyclopentadiene was found to proceed peri-and stereospecifically yielding unstable endo [4+
2] adduct
6. Nitrosotropolone acetate
2 also reacts regio- and stereospecifically in benzene to give endo adduct
3. The structure of the products were determined on the basis of their spectra. Their quinoxaline derivatives were also prepared.
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Shoji Inoue, Kunisuke Okada, Hisae Kakoi, Toshio Goto
1977 Volume 6 Issue 3 Pages
257-258
Published: March 05, 1977
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A luminescent substance was isolated from liver of
N. microchir. It was proved to be identical with
Oplophorus luciferin.
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Shoji Inoue, Hiroyasu Taguchi, Mikiko Murata, Hisae Kakoi, Toshio Goto
1977 Volume 6 Issue 3 Pages
259-262
Published: March 05, 1977
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Watasenia dehydropreluciferin was isolated from livers of
Watasenia scintillans. Its structure was determined as Ia rather than Ib. Sodium borohydride reduction of Ia gave
Watasenia preluciferin (IV).
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Takao Abe, Mitsunori Sukigara, Kenichi Honda
1977 Volume 6 Issue 3 Pages
263-266
Published: March 05, 1977
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The effect of pH on the spectral sensitization of silver chloride was studied electrochemically. The sensitized photocurrent by rhodamine B decreased with lowering pH of the electrolyte solution, whereas in the case of 1,1′-diethyl-2,2′-quinocyanine chloride, the increase in the sensitized photocurrent was observed. The above fact suggests that H
+ existing in the vicinity of the silver chloride surface plays an important role in increasing the sensitized photocurrent.
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Takashi Kawamura, Shigeru Hayashida, Teijiro Yonezawa
1977 Volume 6 Issue 3 Pages
267-270
Published: March 05, 1977
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The hyperfine splitting constant (hfsc) of H
6endo of the bicyclo[2.1.1]hexan-5-yl radical increased from 28.22 G to 28.80 G upon the replacement of H
5 with a deuterium atom, which is qualitatively explained, with the aid of INDO calculations, as due to the decrease of the out-of-plane mode vibration of the C
5–H
5 bond upon the replacement.
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Tadashi Honda, Tatsushi Murae, Takahiko Tsuyuki, Takeyoshi Takahashi
1977 Volume 6 Issue 3 Pages
271-274
Published: March 05, 1977
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13α
H-Olean-18-ene derivatives (
4 and
5) were prepared from olean-12-en-19-one derivatives (
6 and
24, respectively) by a forced Wolff–Kishner reduction and subsequent acetylation and methylation. Methyl 2,3-di-
O-acetylarjunate (
15) was transformed, via
16 and
17, into a 13β
H-olean-18-ene derivative (
21), which proved to be not identical with
4. A 13α
H-configuration was therefore shown for
4. A signal due to a C
(19)–H of the 13α
H-olefins (
4 and
5) was observed at δ 5.30, while that of the 13β
H-olefin (
21) at δ 5.10.
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Izumi Nakai, Kichiro Koto, Kozo Nagashima, Nobuo Morimoto
1977 Volume 6 Issue 3 Pages
275-276
Published: March 05, 1977
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Sarabauite is monoclinic: a=25.33(2), b=5.655(3), c=16.88(1) Å and β=117.51(6)° and C2/c. Z=4 and ρ
c=4.99 g/cm
3. The Sb is essentially coordinated by three atoms of oxygen and/or sulfur. SbO
3 pyramids of the Sb(1), Sb(2) and Sb(3) share corners forming a slab parallel to (100). The four membered ring consisting of Sb(S,O)
3 pyramids of the Sb(4) and Sb(5) links to the slab through the O(2). The Ca is coordinated by eight oxygen atoms in the slab.
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Makoto Hino, Kazushi Arata
1977 Volume 6 Issue 3 Pages
277-278
Published: March 05, 1977
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The title reaction was carried out at room temperature over catalysts prepared by calcining FeSO
4, Fe
2O
3 and Fe(OH)
3 in air at various temperatures, followed by treating with HCl. The FeSO
4 catalyst heat-treated at 700°C showed surprisingly high activity and selectivity, whereas other catalysts were almost inactive.
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Kiyohiko Tajima
1977 Volume 6 Issue 3 Pages
279-282
Published: March 05, 1977
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α-Methoxy-
N-(phenylacetyl)phenylglycine methyl ester was obtained in 37% yield by the treatment of
N-(phenylacetyl)phenylglycine with dicyclohexylcarbodiimide in methanol under an oxygen atmosphere. The mechanism and the generality of this oxidative alkoxylation are discussed.
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Toshifumi Hirata, Reiko Ideo, Takayuki Suga
1977 Volume 6 Issue 3 Pages
283-286
Published: March 05, 1977
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A novel C
31-3,4-secodammarane-type triterpene, alnuseric acid, was isolated from the male flowers of
Alnus serrulatoides Call. (Betulaceae). Its structure was elucidated to be (20
S,24
R)-20 ,24-epoxy-24-methyl-3,4-secodammar-4(28)-en-3-oic acid (I) by a combination of chemical and spectroscopic methods.
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Jyuzo Nakayama, Miyoko Ishihara, Masamatsu Hoshino
1977 Volume 6 Issue 3 Pages
287-288
Published: March 05, 1977
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The title compound was synthesized by the condensation of 3-hydroxytropone with 2-methylthio-1,3-dithiolylium iodide and its spectroscopic properties were described.
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Norio Kunieda, Masayoshi Kinoshita, Junzo Nokami
1977 Volume 6 Issue 3 Pages
289-292
Published: March 05, 1977
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The enantioface differentiating reaction by
p-tolylsulfinylcarbanion(
2), derived from (+)-(
R)-methyl
p-tolyl sulfoxide (
1), toward unsymmetrical ketones (
3) is described. The carbanion(
2) readily reacts with
3 to produce a mixture of (
RSRC)- and (
RSSC)-β-hydroxy sulfoxides (
4). The ratio of the diastereoisomers in
4 and the absolute configuration of the predominant diastereoisomer were determined with the aid of NMR and the specific rotation of alcohol(
6) which was prepared by desulfurization of
4.
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Masaji Oda, Mitsunori Oda, Shoichi Miyakoshi, Yoshio Kitahara
1977 Volume 6 Issue 3 Pages
293-296
Published: March 05, 1977
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3,5,7-Cyclooctatriene-1,2-dione
1, a labile substance, is synthesized from 7-bromo-3,5-cyclooctadiene-1,2-dione by dehydrobromination and characterized by
1H-NMR spectrum and some chemical reactions. The formation of 3-bromo derivative
3 is also demonstrated mainly by means of
1H-NMR spectroscopy.
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Seiji Shinkai, Toyoki Kunitake
1977 Volume 6 Issue 3 Pages
297-300
Published: March 05, 1977
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The reduction of hexachloroacetone by 1-benzyl-1,4-dihydronicotinamide in absolute ethanol and acetonitrile is general acid catalyzed. This mechanism is important in connection with the function of some NADH dependent enzymes in which the reaction can be aided by a general acid catalysis.
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Masanori Kosugi, Kazuo Sasazawa, Yutaka Shimizu, Toshihiko Migita
1977 Volume 6 Issue 3 Pages
301-302
Published: March 05, 1977
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Catalytic allylation of aryl halides with allyltributyltin in the presence of tetrakis(triphenylphosphine)palladium(O) was investigated. The reaction with aryl bromides proceeded efficiently to yield allylbenzenes.
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Akira Nishinaga, Koichi Nakamura, Kaoru Yoshida, Teruo Matsuura
1977 Volume 6 Issue 3 Pages
303-306
Published: March 05, 1977
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The
p-peroxyquinol esters derived from the base-catalyzed oxygenation of 4-alkyl-2,6-di-
t-butylphenols (alkyl=R
1) followed by the Schotten–Baumann acylation (R
2COCl) undergo a novel base-catalyzed rearrangement with
t-BuOK in DMF to give
p-quinoxyacetic acid derivatives in excellent yields. A mechanism involving the initiation by the homolysis of O–O bond is discussed.
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Masaji Oda, Masaji Kasai, Yoshio Kitahara
1977 Volume 6 Issue 3 Pages
307-310
Published: March 05, 1977
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2-Diazo-4-cyclopentene-1,3-dione
1 and 2-diazo-4,6-cycloheptadiene-1,3-dione
2 are synthesized. The spectral data of these compounds indicate that there are considerable difference between them in the degree of resonance contribution of the canonical forms: the contribution of the enolate canonical form
1b to the resonance hybrid cf
1 is less important than the corresponding form of usual 2-diazo-1,3-diones, while the enolate form
2b to
2 is very important.
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Yukio Kubota
1977 Volume 6 Issue 3 Pages
311-316
Published: March 05, 1977
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The fluorescence properties (spectrum, lifetime and quantum yield) of 9-aminoacridine cation in aqueous solutions of nucleotides have been examined. It was found that the fluorescence of the dye is quenched by adenosine-5′-monophosphate and guanosine-5′-monophosphate. Quantitative analysis of the results shows that the quenching of fluorescence is caused by dynamic and static quenching processes.
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Shoichi Kikkawa, Masakatsu Nomura, Michimasa Shimizu
1977 Volume 6 Issue 3 Pages
317-318
Published: March 05, 1977
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The reaction of three butenes with chlorine through ZnCl
2–KCl–NaCl melts yielded selectively butadiene at 450°C while chlorination through CuCl–KCl–NaCl melts and thermal chlorination produced considerable amounts of C
4H
7Cl and C
4H
8Cl
2 along with expected butadiene.
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Katsuhiko Miyoshi, Yoshiaki Wada, Hayami Yoneda
1977 Volume 6 Issue 3 Pages
319-320
Published: March 05, 1977
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Partial resolution of neutral [Co(acac)
3] was performed by extracting into 1,2-dichloroethane the complex formed when racemic Li[Co(acac)
3] was mixed with Δ- or Λ-[Co(phen)
3]Cl
3 in water. This system is the first Pfeiffer-active system in which a dissymmetric metal complex serves as a chiral environment compound.
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