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Tsuno, Yuho, Fujio, Mizue, Yukawa, Yasuhide (1975) The Substituent Effect. VI. Inductive and π-Electronic Effects in the Phenol Hydroxyl Chemical Shifts in DMSO. Bulletin of the Chemical Society of Japan, 48 (11). 3324-3329 doi:10.1246/bcsj.48.3324

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Reference TypeJournal (article/letter/editorial)
TitleThe Substituent Effect. VI. Inductive and π-Electronic Effects in the Phenol Hydroxyl Chemical Shifts in DMSO
JournalBulletin of the Chemical Society of Japan
AuthorsTsuno, YuhoAuthor
Fujio, MizueAuthor
Yukawa, YasuhideAuthor
Year1975 (November)Volume48
Issue11
PublisherThe Chemical Society of Japan
DOIdoi:10.1246/bcsj.48.3324Search in ResearchGate
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Mindat Ref. ID4483590Long-form Identifiermindat:1:5:4483590:9
GUID0
Full ReferenceTsuno, Yuho, Fujio, Mizue, Yukawa, Yasuhide (1975) The Substituent Effect. VI. Inductive and π-Electronic Effects in the Phenol Hydroxyl Chemical Shifts in DMSO. Bulletin of the Chemical Society of Japan, 48 (11). 3324-3329 doi:10.1246/bcsj.48.3324
Plain TextTsuno, Yuho, Fujio, Mizue, Yukawa, Yasuhide (1975) The Substituent Effect. VI. Inductive and π-Electronic Effects in the Phenol Hydroxyl Chemical Shifts in DMSO. Bulletin of the Chemical Society of Japan, 48 (11). 3324-3329 doi:10.1246/bcsj.48.3324
In(1975, November) Bulletin of the Chemical Society of Japan Vol. 48 (11) The Chemical Society of Japan

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TSUNO, YUHO, FUJIO, MIZUE, YUKAWA, YASUHIDE (1976) ChemInform Abstract: SUBSTITUENT EFFECT. VI. INDUCTIVE AND Π-ELECTRONIC EFFECTS IN THE PHENOL HYDROXYL CHEMICAL SHIFTS IN DMSO (DIMETHYL SULFOXIDE) Chemischer Informationsdienst, 7 (7) doi:10.1002/chin.197607048
Fujio, Mizue, Mishima, Masaaki, Tsuno, Yuho, Yukawa, Yasuhide, Takai, Yoshio (1975) The Substituent Effect. V. NMR Chemical Shifts of Hydrogen-bonding Hydroxyl Proton of Phenols in DMSO. Bulletin of the Chemical Society of Japan, 48 (7). 2127-2133 doi:10.1246/bcsj.48.2127
Fujio, Mizue, Tsuno, Yuho, Yukawa, Yasuhide, Takai, Yoshio (1975) The Substituent Effect. VII. Substituent Chemical Shifts of NH Proton of Acetanilides. Bulletin of the Chemical Society of Japan, 48 (11). 3330-3336 doi:10.1246/bcsj.48.3330
Tsuno, Yuho, Fujio, Mizue, Takai, Yoshio, Yukawa, Yasuhide (1972) The Substituent Effect. IV. Proton NMR Chemical Shifts of Phenols. Bulletin of the Chemical Society of Japan, 45 (5). 1519-1529 doi:10.1246/bcsj.45.1519
FUJIO, MIZUE, MISHIMA, MASAAKI, TSUNO, YUHO, YUKAWA, YASUHIDE, TAKAI, YOSHIO (1975) ChemInform Abstract: THE SUBSTITUENT EFFECT PART 5, NMR CHEMICAL SHIFTS OF HYDROGENBONDING HYDROXYL PROTON OF PHENOLS IN DMSO. Chemischer Informationsdienst, 6 (40) doi:10.1002/chin.197540050
Tsuno, Yuho, Kusuyama, Yoshiaki, Sawada, Masami, Fujii, Takahiro, Yukawa, Yasuhide (1975) The Substituent Effect. VIII. Solvolysis ofm- andp-Substituted α-Methylbenzyl Chlorides. Bulletin of the Chemical Society of Japan, 48 (11). 3337-3346 doi:10.1246/bcsj.48.3337
Tsuno, Yuho, Sawada, Masami, Fujii, Takahiro, Yukawa, Yasuhide (1975) The Substituent Effect. X. Solvolysis of 3- and 4-Substituted 1-(1-Naphthylethyl) Chlorides. Bulletin of the Chemical Society of Japan, 48 (11). 3347-3355 doi:10.1246/bcsj.48.3347
FUJIO, MIZUE, TSUNO, YUHO, YUKAWA, YASUHIDE, TAKAI, YOSHIO (1976) ChemInform Abstract: SUBSTITUENT EFFECT. VII. SUBSTITUENT CHEMICAL SHIFTS OF NH PROTONS OF ACETANILIDES. Chemischer Informationsdienst, 7 (7) doi:10.1002/chin.197607049
Tsuno, Yuho, Sawada, Masami, Fujii, Takahiro, Tairaka, Yoshihiko, Yukawa, Yasuhide (1975) The Substituent Effect. XI. Solvolysis of 5-, 6-, and 7-Substituted 1-(1-Naphthylethyl) Chlorides. Bulletin of the Chemical Society of Japan, 48 (11). 3356-3366 doi:10.1246/bcsj.48.3356
Yamada, Hiroaki, Tsuno, Yuho, Yukawa, Yasuhide (1970) Substituent Effects on the NMR Chemical Shifts of Aromatic Side Chain Protons. I. The Effects ofmeta-Substituents. Bulletin of the Chemical Society of Japan, 43 (5). 1459-1472 doi:10.1246/bcsj.43.1459
Tsuji, Yutaka, Fujio, Mizue, Tsuno, Yuho (1990) Substituent Effects. 22. The Solvolysis of α-t-Butylbenzyl Tosylates. Bulletin of the Chemical Society of Japan, 63 (3). 856-866 doi:10.1246/bcsj.63.856
 
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