巻号一覧
20 巻, 10 号
選択された号の論文の40件中1～40を表示しています
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飯 照彦, 佐藤 善重1972 年 20 巻 10 号 p. 2079-2090
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーAbsorption, distribution, excretion and metabolism of trimethoprim were studied in rats. Trimethoprim was absorbed rapidly and almost completely from the digestive tract, the half-life for absorption being 18 min. After absorption the drug left the blood rapidly and was taken up by various organs except brain. The highest concentration was found in the kidney. Appreciable levels were found in the bone marrow, thyroid, liver and lung. The lowest drug concentration was noted in the brain. Approximately 95% of the radioactivity after oral administration of 14C-trimethoprim was recovered from the urine and feces within 72 hr. The urinary excretion is the major excretory route since more than 85% of the total radioactivity recovered appeared in the 72 hr urine. About 30% of the radioactivity excerted in 8 hr urine was present as intact 14C-trimethoprim. Metabolic pathways of trimethoprim consisted of O-demethylation, ring N-oxidation and α-hydroxylation. 3-Demethyl-trimethoprim was the largest metabolite which accounted for more than 30% of the radioactivity excreted in 8 hr urine. 4-Demethyltrimethoprim was excerted mainly as glucuronide which accounted for about 19%. Trimethoprim ring N-oxide and α-hydroxy-trimethoprim were excreted in amounts of 7 and 5%, respectively. Simultaneous administration of sulfamethoxazole did not influence the absorption, distribution, excretion and metabolism of trimethoprim in rat.抄録全体を表示PDF形式でダウンロード (1270K) -
村山 正雄, 村井 博, 仙福 健治, 角倉 達朗, 尾崎 正邦1972 年 20 巻 10 号 p. 2091-2095
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーSynthetic meranzin (IVa) was treated with dimethylamine or piperidine in methanol at 40-42°(condition A) and in benzene at 150°(condition B). cis-Amides (VII) and (IX) and trans-amides (VIII) and (X) were obtained under conditions A and B, respectively. Re-examination of the reaction of natural IVa with dimethylamine under condition B revealed that the product was not V proposed by Bohme, et al. but one of the optical isomers of VIII. Treatment of natural IVa with dimethylamine under condition A gave one of the optical isomers of racemic VII. VII-VIII or IX-X equilibrium in ethanol induced by diffused light was also described.抄録全体を表示PDF形式でダウンロード (739K) -
久保田 晴寿, 宇多 正行1972 年 20 巻 10 号 p. 2096-2101
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーTautomerism of 3-α-pyridyl-1, 2, 4-triazoline-5-thione (I) and its methyl derivatives has been studied. The infrared spectra of these compounds indicated the presence of strong intermolecular hydrogen bonding in a solid state. Comparison of the ultraviolet (UV) spectrum of 5-methylthio-3-α-pyridyl-1, 2, 4-triazole (II) with those of the fixed compounds revealed that II exists as 2H-5-methylthio-3-α-pyridyl-1, 2, 4-triazole both in ethanol and in cyclohexane. In the same way, it was found 1-, 2-, and 4-methyl-3-α-pyridyl-1, 2, 4-triazoline-5-thiones (III, IV, and V), which are capable of existing in thione-thiol tautomerism, exist in thione form in ethanol. The parent compound I was also found by means of UV spectroscopy to exist in the thione form of 1H, 4H-3-α-pyridyl-1, 2, 4-triazoline-5-thione in ethanol.抄録全体を表示PDF形式でダウンロード (592K) -
古川 潮, 小島 洋子, 林 清五郎1972 年 20 巻 10 号 p. 2102-2105
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリー1, 1-Dialkylguanidine reacted with benzil in the presence of sodium ethoxide to give 2-dialkylamino-4-oxo-5, 5-diphenylimidazoline, from which N-acetyl compound was successfully obtained by heating with an great excess of acetic anhydride. The structures of these compounds were confirmed by mass spectra and infrared spectra.抄録全体を表示PDF形式でダウンロード (561K) -
高橋 幸太郎, 金山 慶喜, 田辺 良久, 高荷 昌子1972 年 20 巻 10 号 p. 2106-2111
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーA new triterpene named astilbic acid (I) has been isolated from the roots of Astilbe Thunbergii var. congests H. BOISSIEU (Saxifragaceae) in addition to β-peltoboykinolic acid and the structure of astilbic acid has now been established as 3β, 6β-dihydroxyolean-12-en-27-oic acid on the basis of chemical and physicochemical evidences.抄録全体を表示PDF形式でダウンロード (707K) -
伊藤 敬一, 大庭 均, 関屋 実1972 年 20 巻 10 号 p. 2112-2116
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThere has been introduced a new type of formic acid reduction of the compounds in which both amine nitrogen and ether oxygen are bound to the same carbon. With series of N-(α-butoxybenzyl) dialkylamines, N-(butoxymethyl) dialkylamines and 3-methyloxazolidines, the reaction was normally carried out on heating with distillable formate, TMAF given by 5HCO2H·2N (CH3)3, to give tertiary amines, resulting in reductive fission at the carbon-oxygen bond. Mode of the reduction was clarified by the technique of using deuterated formic acids, in which formyl hydrogen of formic acid is transferred to the carbon of the carbon-oxygen bond. On the basis of this result a possible mechanism is described.抄録全体を表示PDF形式でダウンロード (703K) -
遠藤 賢裕, 内山 充1972 年 20 巻 10 号 p. 2117-2122
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーPhospholipid extracted with CHCl3-MeOH (2 : 1 v/v) from the brain and liver of pyrithioxine-treated animals, as compared to that from control animals, was greater in amount. The amount of phospholipid extracted with CHCl3-MeOH (7 : 1 v/v) saturated with NH4OH from tissue residue after CHCl3MeOH (2 : 1) extraction is found to be smaller in pyrithioxine-treated animals. This decrement of phospholipid is represented by phosphatidylserine and phosphatidylinositol, which both account for the increment of CHCl3-MeOH (2 : 1)-extracted phospholipid.抄録全体を表示PDF形式でダウンロード (789K) -
渡辺 徳弘, 浜口 文子, 大木 貞雄1972 年 20 巻 10 号 p. 2123-2127
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーAs a new and convenient method for the synthesis of 4-indolecarboxylic acid (1), the synthesis was started with the reduction of 3-nitrophthalimide (4) with sodium borohydride, followed by hydrolysis of the product to obtain 3-hydroxy-4-nitrophthalide (6). Treatment of 6 with 2 moles of diazomethane gave 2-methoxycarbonyl-6-nitrostyrene oxide (7) whose reductive cyclization afforded methyl 4-indolecarboxylate (2) and it was saponified to the desired 1.抄録全体を表示PDF形式でダウンロード (581K) -
関屋 実, 寺尾 良保1972 年 20 巻 10 号 p. 2128-2133
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーIt has now been found that reduction of 3-aryl-3-hydroxyphthalimidines to 3-arylphthalimidines are easily effected on heating with the formate reagent, TMAF, known as a constant boiling liquid composed of formic acid and trimethylamine. Fashon of the attack of formic acid in this reaction was clarified by means of using deuterated formate reagent.抄録全体を表示PDF形式でダウンロード (596K) -
近藤 嘉和, 竹本 常松1972 年 20 巻 10 号 p. 2134-2136
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーPotassium permanganate oxidation of acetoneberberine gave rise to so called neoxyberberine acetone and 2-(2, 3-dimethoxy-6-carboxy-α-acetonyl-benzyl)-1-oxo-6, 7-methylenedioxy-1, 2, 3, 4-tetrahydroisoquinoline (IV). The structure of IV was established by chemical and spectral data.抄録全体を表示PDF形式でダウンロード (457K) -
吉本 昌文, 石田 登, 岸田 有吉1972 年 20 巻 10 号 p. 2137-2142
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThree 2-propynyl sulfones (VIIIa-c) reacted with methyl acrylate to give the corresponding 2-carbomethoxy-4-ethynyl-4-arylsulfonylcyclohexanones (IXa-c), respectively. Nucleophilic reaction of acetylenic sulfonyl carbanion showed ambident character depending on the nature of electrophiles which were classified into two kinds. Some discussions of the reaction and physical properties of the products are presented.抄録全体を表示PDF形式でダウンロード (577K) -
樋口 隆一, 川崎 敏男1972 年 20 巻 10 号 p. 2143-2149
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe more polar four triterpenoid saponins, D-G, of the seven, A-G, so far isolated in pure state from the seeds of Akebia quinata DECNE. were characterized as follows : saponin D (mp>225°(decomp.), [α]D+15°), 3-O-α-L-arabinopyranosyl hederagenin 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside (IV) ; E (mp 210-214°(decomp.), [α]D+6°), 3-O-β-D-xylopyranosyl-(1→2)-α-L-arabinopyranosyl hederagenin 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside (XI) ; F (mp 211-214°(decomp.), [α]D-4°), 3-O-β-D-glucopyranosyl-(1→2)-α-L-arabinopyranosyl hederagenin 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside (XIV) ; G (mp>218°(decomp.), [α]D-19°), 3-O-β-D-glucopyranosyl-(1→2)-[α-L-rhamnopyranosyl-(1→4)]-α-L-arabinopyranosyl hederagenin 28-O-α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside (XVI). They are new hederagenin 3, 28-O-bisglycosides and related to each other and to saponins A, B, and C.抄録全体を表示PDF形式でダウンロード (919K) -
枡井 雅一郎, 須田 晃治, 飯島 千之1972 年 20 巻 10 号 p. 2150-2155
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーN-(1-Cyanoalkyl) alkylideneamine N-oxide reacts with carboxamides to give N-(1-cyanoalkyl)-N-(1'-carboxamido-alkyl) hydroxylamines. The reaction is catalyzed by strong bases. On warming in solvents these adducts readily decompose to the starting nitrones and amides, and the decomposition is accelerated by elevation of temperature.抄録全体を表示PDF形式でダウンロード (587K) -
南原 利夫, 工藤 俊博1972 年 20 巻 10 号 p. 2156-2162
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーIsomeric 15α- and 17α-bromo-13α-estratrien-16-ones (IX, X) were prepared from the parent 16-ketone (VII) by way of the enol acetate (VIII). The configuration of both bromine atoms introduced was determined by the standard method of Fieser and Ettorre. These positional isomers were readily distinguished by converting into the ⊿15- and ⊿16- unsaturated compounds (XIII, XIV), respectively. On the basis of the spectral data listed in Table I the nature of C-bromine bonds and the conformation of ring D have been discussed. Two synthetic routes leading to the 17α-acetoxy-16-ketone (V) have also been described.抄録全体を表示PDF形式でダウンロード (893K) -
成戸 俊二, 米光 宰1972 年 20 巻 10 号 p. 2163-2171
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe photoreaction of indole with methyl chloroacetate afforded a mixture of seven isomeric methyl indoleacetates, mainly the 4-isomer, whose separation into each component was carried out by repeated column chromatographies. The structues of all of them confirmed by their spectral data and by the unequivocal sysntheses. The unusual reactivity of the 4-position on the indole nucleus was explained on the basis of the calculation data by SCF-CI-MO method.抄録全体を表示PDF形式でダウンロード (1074K) -
前林 行雄, 宮木 高明, 山崎 幹夫1972 年 20 巻 10 号 p. 2172-2175
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーIncorporation of L-phenylalanine-U-14C, Na-acetate-2-14C into ochratoxin A was demonstrated in Aspergillus ochraceus, suggesting that the biosynthesis of ochratoxin A involves so called "acetate-malonate" and "shikimic acid" pathways. By the aid of 13C-NMR spectrometric method, the participation of Na-formate-13C for the formation of carboxyl group was confirmed.抄録全体を表示PDF形式でダウンロード (534K) -
北川 常廣, 三浦 孝子, 谷山 兵三1972 年 20 巻 10 号 p. 2176-2184
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe new purification method, alkylations and acylations of tuberculostatic antibiotic viomycin were performed. The characterizations were conducted with viomycin as well as the derivatives obtained by these reactions. And also it was clarified that the alkylations on the reactive hydroxyl group of tuberactidine function had no significant influence on the antimicrobial activities while, the acylations on the N-terminal amino functions nullified the potency.抄録全体を表示PDF形式でダウンロード (1044K) -
木村 道也, 藤間 貞彦, 富田 勤1972 年 20 巻 10 号 p. 2185-2190
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーWhen cholesterol (I) was treated with the hydrogen peroxide-ferrous sulphate system in an acetic acid solution, there were formed 5α-cholestane-3β, 5, 6β-triol (II), 3β-acetoxy-5α-cholestane-5, 6β-diol (III), 5, 6α-epoxy-5α-cholestan-3β-ol (IV), 6β-acetoxy-5α-cholestane-3β, 5-diol (V), and 3β, 6β-diacetoxy-5α-cholestan-5α-ol (VI). Ferrous ions accelerated remarkably the formation of these products (Fig. 2) as well as peracetic acid (Fig. 3). The same ions were, however, likely to be independent of forming the epoxide (IV) from I with peracetic acid (Fig. 4). Hydrogen peroxide and ferrous ions were cooperative in facilitating the formation of II from IV, conrtary to be entirely invalid in their independent use (Fig. 5). Thus, it seemed in the present reaction that the epoxide (IV) is produced heterolytically, as usual, with peracetic acid which can easily be formed in the mixture of acetic acid and hydrogen peroxide (Chart 1) and that the triol (II) as well as the derivatives (III, V, and VI) are formed mainly through IV.抄録全体を表示PDF形式でダウンロード (744K) -
城島 輝臣, 竹柴 英雄, 此常 卓男1972 年 20 巻 10 号 p. 2191-2203
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーHeating 3-chloro-6-(2-allylphenoxy) pyridazine (IIIa) with or without a solvent afforded xanthene (Va) by a novel intramolecular cycloaddition reaction followed by elimination of nitrogen and hydrogen chloride. Formation of a fully aromatized product indicated that elimination of both N2 and HCl has occurred from the initially formed π4+π2 cycloadduct (IV). Variously substituted xanthenes were prepared by heating the corresponding 3-chloro-6-(2-allylphenoxy) pyridazines in diethylaniline (DEA). The compound having an allylic group at the para-position of the benzene ring did not give any cyclized product, because the allylic double bond was too far from the pyridazine ring. Similar treatment of 3-chloro-6-(2-propenylphenoxy) pyridazine (XXVI) gave rise to 1-methyldibenzofuran (XXVIII) in a low yield.抄録全体を表示PDF形式でダウンロード (1362K) -
内丸 文彦, 岡田 清三郎, 小笹山 瑛, 今野 常生1972 年 20 巻 10 号 p. 2204-2208
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe nuclear magnetic resonance parameter of disubstituted pyrazines have been correlated with the chemical structure. The coupling constants of 2, 3-, 2, 5-, 2, 6-disubstituted pyrazines are 2.5-3.0, 1.1-1.4, 0 Hz respectively, and these values are not influenced by the kind of the substituents. The calculated chemical shifts which are obtained from the additivity rule of the shielding parameter of the substituents are well agreed with the observed ones.抄録全体を表示PDF形式でダウンロード (583K) -
中川 康, 安芸 修躬, 白川 研蔵1972 年 20 巻 10 号 p. 2209-2214
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリー1-Alkyl-2, 1-benzisoxazolium salts were prepared by the reaction of 2, 1-benzisoxazoles with trialkyl orthoformates in the presence of Lewis acids as well as with Meerwein's reagents or dialkoxycarbonium hexachloroantimonates. Reactions of these quarternary salts with various nucleophilic reagents afforded 3-substituted 1-alkyl-2, 1-benzisoxazoline derivatives.抄録全体を表示PDF形式でダウンロード (668K) -
北川 常廣, 三浦 孝子, 藤原 邦雄, 谷山 兵三1972 年 20 巻 10 号 p. 2215-2225
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe novel partial hydrolysis of peptide bonds by using N→O acyl migrative reactions followed by the methanolysis of the resulting ester linkages were studied to give the successful application with tetrahydro derivative of viomycin, a tuberculostatic antibiotic. Also, the partial hydrolysis of perhydroacetylviomycin yielded two peptide fragments. The sequential analysis of these fragments by Edman-dansyl procedures and the end group analysis concluded that the primary structure of viomycin is formulated as XXV. The sequence is well compatible to the chemical formula I, the one of recently proposed two structures.抄録全体を表示PDF形式でダウンロード (1290K) -
北川 勲, 松田 明子, 吉岡 一郎1972 年 20 巻 10 号 p. 2226-2234
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe sapogenol constituents of five Japanese Primulaceous plants : i) Primula sieboldi E. MORREN, roots (Japanese name : sakuraso), ii) P. japonica A, GRAY, roots and fruits (kurinso), iii) Lysimachia mauritiana LAM., Fruits (hamabossu), iv) L. clethroides DUBY, roots (okatoranoo), v) L. japonica THUNB., roots (konasubi), have been investigated. It has been elucidated that the major sapogenols obtained by acid hydrolysis of saponin of each plant material are primulagenin A (VIII) and/or dihydropriverogenin A (XIII), while periodate oxidation followed by alkaline treatment of saponin furnished the inconsistent sapogenol compositions and the genuine sapogenols have been shown to possess a 13β, 28-oxide moiety as seen in protoprimulagenin A (XV), a newly isolated sapogenol from i), ii), iv), and v), and priverogenin B (XII). The structure of protoprimulagenin A (XV) has been established on the basis of chemical and physicochemical evidences.抄録全体を表示PDF形式でダウンロード (1212K) -
南原 利夫, 本間 誠次郎, 金山 紀世子1972 年 20 巻 10 号 p. 2235-2239
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe role of the conjugate in the biosynthesis of 2-methoxyestrogen in the living animal has been explored by the double-isotope technique. The isotope ratios of the isomeric catechol estrogen monomethyl ethers excreted in urine after simultaneous administration of estrone-4-14C and estrone-6, 7-3H sulfate or estradiol-6, 7-3H 3-glucuronide were determined. Comparison of the 3H/14C value with that of the administered steroid implies that the sulfate conjugation may possibly participate in the predominant formation of 2-methoxyestrogen, while the conjugation with glucuronic acid may not. The dimethyl ether of catechol estrogen was metabolized with random O-demethylation yielding two isomeric monomethyl ethers both in the rat and man. Therefore it appears that the selective O-demethylation may not be involved in the preferential formation of 2-methoxyestrogen.抄録全体を表示PDF形式でダウンロード (702K) -
藤間 貞彦, 藤野 明治, 山崎 克彦, 木村 道也1972 年 20 巻 10 号 p. 2240-2245
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe β-axial hydroxylated 5β-spirostan-1- and 3-ones were prepared from the steroidal sapogenins in Convallaria and diosgenin, and the optical rotatory dispersion curves of these ketones were measured in methanol or dioxane. The 5-hydroxy-25 (R), 5β-spirostan-3-one (XIII) showed a weak positive amplitude (a : +16.0) in contrast to the negative one of the parent 3-ketone (I, a : -16.6). The hydroxyl groups substituted on the symmetrical β-axial positions to the carbonyl groups led to marked changes in the amplitude of Cotton effect in the 5β-spirostanones, and opposed to the prediction from the octant rule.抄録全体を表示PDF形式でダウンロード (724K) -
中村 昭四郎, 浅野 健治, 福田 頴穂1972 年 20 巻 10 号 p. 2246-2250
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe cultured filtrates of Streptomyces were screened for the anti-thymidine kinase activity using the homogenate of Yoshida sarcoma cells and (methyl-3H)-thymidine to obtain antitumor antibiotics. The active component produced by Streptomyces yokosukanensis was isolated and determined to be a new acid phosphatase (E.C. 3.1.3.2.). Production, isolation, purification, effect of pH on the activity, stability, effect of temperature on the activity, effect of inhibitors on the activity and substrate specifity are described.抄録全体を表示PDF形式でダウンロード (591K) -
藤田 真一, 藤田 安二1972 年 20 巻 10 号 p. 2251-2255
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーThe essential oils of Magnolia salicifolia MAXIM. gathered at Mt. Ohira and its vicinity, Kawanishi-shi, Hyogo Prefecture have been examined. The characteristics of the shoot oils are abundant existence of methylchavicol (13.5-22.5%), safrole (17.0-24.6%), and methyleugenol (21.0-43.5%).抄録全体を表示PDF形式でダウンロード (526K) -
南原 利夫, 細田 宏, 安生 孝子, 池川 繁男1972 年 20 巻 10 号 p. 2256-2261
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーIn order to clarify the stereochemistry of hydrogen loss from C-2 and C-4 during the microbial ⊿1- and ⊿4-dehydrogenation the titled compounds have been synthesized as the suitable substrates. The key intermediates leading to the desired compounds, ⊿2- and ⊿3-olefins (V, VI), were prepared from 5β-androstane-3α, 17β-diol 3-tosylate 17-acetate (IV). Epoxidation with per-acid followed by trans-diaxial opening of the resulting β-epoxides (VII, VIII) with lithium aluminum deuteride gave 2α- and 4α-deuterio-5β-androstane-3β, 17β-diols (X, XIV). On the other hand V and VI were transformed into the 2β- and 4β-deuterio-3β, 17β-diols (XII, XVI) by treatment with deuterated diborane and then with hydrogen peroxide. Upon oxidation with chromium trioxide-pyridine complex these labeled diols were led to the 2- and 4-deuterated 3, 17-diketones (XI, XIII, XV, XVII), respectively.抄録全体を表示PDF形式でダウンロード (808K) -
古川 潮, 長門 賢司, 小島 洋子, 林 紘司1972 年 20 巻 10 号 p. 2262-2264
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーPDF形式でダウンロード (474K) -
尾形 秀, 松本 博1972 年 20 巻 10 号 p. 2264-2268
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーPDF形式でダウンロード (568K) -
堀井 善一, 今西 武, 花岡 美代次, 岩田 宙造1972 年 20 巻 10 号 p. 2269-2271
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーPDF形式でダウンロード (496K) -
成戸 俊二, 米光 宰1972 年 20 巻 10 号 p. 2272-2274
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーPDF形式でダウンロード (472K) -
山崎 幹夫, 前林 行雄, 宮木 高明1972 年 20 巻 10 号 p. 2274-2276
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーPDF形式でダウンロード (465K) -
山崎 幹夫, 前林 行雄, 宮木 高明1972 年 20 巻 10 号 p. 2276-2278
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーPDF形式でダウンロード (437K) -
北川 勲, 中西 勤, 伊藤 良久, / 吉岡 一郎, ITIRO YOSIOKA1972 年 20 巻 10 号 p. 2278-2281
発行日: 1972/10/25
公開日: 2008/03/31
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星 昭夫, 吉田 光二, 宮沢 文彦, 榑谷 和男, 金井 貞, 市野 元信1972 年 20 巻 10 号 p. 2286-2287
発行日: 1972/10/25
公開日: 2008/03/31
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平尾 子之吉, 外山 利雄, 高畠 明, 安井 凡平1972 年 20 巻 10 号 p. 2287-2289
発行日: 1972/10/25
公開日: 2008/03/31
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山岸 喬, 林 紘司, 三橋 博1972 年 20 巻 10 号 p. 2289-2291
発行日: 1972/10/25
公開日: 2008/03/31
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村田 忠一, 篠原 正和, 宮本 益雄1972 年 20 巻 10 号 p. 2291-2292
発行日: 1972/10/25
公開日: 2008/03/31
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鵜飼 茂夫, 広瀬 一雄, 木方 正, 原 千尋, 入倉 勉, 兼近 庸喜, 長谷川 嘉成1972 年 20 巻 10 号 p. 2293-2294
発行日: 1972/10/25
公開日: 2008/03/31
ジャーナル フリーPDF形式でダウンロード (331K)
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