Пожалуйста, помогите найти статьи из японских журналов

[vitaliano]

1) Yokote, Kaneko. Kogyo Kagaku Zasshi (J. Chem. Soc. Japan) 1953, V.56, P. 770;
2) Tamura. Yakugaku Zasshi (J. Pharm. Soc. Japan) 1960. V.80. P.562.

[Shlavik]

Японцы хорошо представлены в БЕН РАН, НО до 77 год там не дают надо искать по сводному РАН и по институтам но занете редкостные журналы могу только найти абстракт
ибо в сводном в ГПНТБ я глядел, в РГБ глядел нету!

Иожете в ИНЭОСе спросить атм етсь япоснкие и достаточно редкие!

Могу только абстракт, прчием статья на Японском

Nitration of 9-chloro-1-azaanthracene. II. Nitration with nitric acid at boiling temperature. Yokote, Masao; Kaneko, Yoshio. Nippon Univ., Tokyo, Kogyo Kagaku Zasshi (1953), 56 770-3. Journal language unavailable.
CAN 49:36012

Abstract

9-Chloro-1-azaanthracene (I) (1 g.) was boiled with 10 cc. HNO3 (d. 1.52) for 3-22 hrs. and the product obtained was sepd. into sol. and insol. parts in hot EtOH. The 6,10-dinitro deriv. of I, m. 269-272 (cor.), (0.12 g.) was obtained from the insol. part, and it yielded 6-nitro-1-azaanthraquinone, m. 271-2 (cor.), by oxidation with CrO3, and further, 6-amino-1-azaanthraquinone, m. 283-6 (cor.), by reduction with Na2S. The alc. sol. part gave 5-nitro-1-azaanthraquinone by oxidation. The similar treatment of 1 g. I with 4 cc. glacial AcOH and 0.3 g. HNO3 (d. 1.52) at b.p. for 1-2 hrs. gave chiefly the 10-nitro deriv. of I, m. 200-3, and with excess HNO3, the 6,10-dinitro deriv. of I. A compd. which gives 8-nitro-1-azaanthraquinone on being oxidized is also produced.


2 статья в двух частях! Язык неопределен, тут даже японский диалект однако!

Syntheses of quinolines. I. Tamura, Shinzo. Univ. Kyushu, Yakugaku Zasshi (1960), 80 559-61. 0031-6903. Journal language unavailable. CA 54:118313

Abstract

A mixt. of 3 g. PhNH2 and 5.1 g. CH2:CHCH(OAc)2 (I) in 30 mL. AcOH kept 2 h. at room temp., this added dropwise to a boiling soln. of 17.4 g. FeCl2.6H2O in 30 mL. 5% HCl, refluxed 8 h., heated to 160°, the residue in dil. NaOH steam distd., the distillate in Et2O concd., the residue in 1 mL. Ac2O and EtOH heated, the soln. concd., the residue in Et2O extd. with 5% HCl, made alk., and the product extd. with Et2O yielded 31.9% C9H7N, b20 120-2°; picrate m. 203°. The Et2O residue (after extg. with 5% HCl) gave 5.5% AcNHPh, m. 114°. Similarly, 4.65 g. PhNH2, 8.6 g. MeCH:CHCH(OAc)2, 40 mL. AcOH, 27 g. FeCl3.6H2O, and 25 mL. 10% HCl yielded 50.2% quinaldine, b25, 138-40°; picrate m. 193°. PhNH2 (0.89 g.) and 1.63 g. CH2:CMeCH(OAc)2 yielded 38.7% 3-MeC9H6N; picrate m. 187°.


Syntheses of quinolines. II. Tamura, Shinzo; Kudo, Tadahiro; Yanagihara, Yasutake. Univ. Kyushu, Yakugaku Zasshi (1960), 80 562-4. Journal language unavailable. CA 54:118314

Abstract

o-MeC6H4NH2 (5.35 g.) and 7.9 g. CH2:CHCH(OAc)2 (as above) yielded 30.9% 8-MeC9H6N, b5 89°; picrate m. 198-202°. Similarly, m-MeC6H4NH2 yielded 22% 7-MeC9H6N, b4 86-90°; picrate m. 237°. p-MeC6H4NH2 yielded 17.2% 6-MeC9H6N, b4 88-9°; picrate m. 230-1°. 2,3-ClMeC6H3NH2 (7.87 g.) and 8.81 g. CH2:CHCH(OAc)2 yielded 16% 7,8-MeClC9H5N, b2 162°; H2SO4 salt m. 179-80°. Similarly, 2-C10H7NH2 gave 39.9% benzo[f]quinoline, b7 173°; picrate m. 253°. o-MeOC6H4NH2 gave 35.2% 8-MeOC9H6N, b5 137-40°. p-MeOC6H4NH2 gave 11.2% 6-MeOC9H6N, b6 140°. p-O2NC6H4NH2 gave 6.3% 6-O2NC9H6N, m. 150°. 4-H2NC5H4N(O) gave a small amt. of 1,6-naphthyridine 6-oxide, m. 152-4°. PhNHOH gave 47.6% C9H7N and 2.7% AcNHPh. PhNHOH (8.72 g.) and 13.76 g. MeCH:CHCH(OAc)2 gave 31% 2-MeC9H6N; picrate, m. 193°.

[vitaliano]

Огромное спасибо!

[Shlavik]

2) Tamura. Yakugaku Zasshi (J. Pharm. Soc. Japan) 1960. V.80. P.562.

Вот это точно ИОХ РАН!
Я узнавал к сожалению уже не вхож в этот институт!