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Suga, Takayuki, Yoshioka, Takamitsu, Hirata, Toshifumi, Aoki, Tadashi (1983) 13C NMR Signal Assignments of Herqueinone and Its Phenalenone Derivatives. Bulletin of the Chemical Society of Japan, 56 (12). 3661-3666 doi:10.1246/bcsj.56.3661

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Reference TypeJournal (article/letter/editorial)
Title13C NMR Signal Assignments of Herqueinone and Its Phenalenone Derivatives
JournalBulletin of the Chemical Society of Japan
AuthorsSuga, TakayukiAuthor
Yoshioka, TakamitsuAuthor
Hirata, ToshifumiAuthor
Aoki, TadashiAuthor
Year1983 (December)Volume56
Issue12
PublisherThe Chemical Society of Japan
DOIdoi:10.1246/bcsj.56.3661Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID4490711Long-form Identifiermindat:1:5:4490711:8
GUID0
Full ReferenceSuga, Takayuki, Yoshioka, Takamitsu, Hirata, Toshifumi, Aoki, Tadashi (1983) 13C NMR Signal Assignments of Herqueinone and Its Phenalenone Derivatives. Bulletin of the Chemical Society of Japan, 56 (12). 3661-3666 doi:10.1246/bcsj.56.3661
Plain TextSuga, Takayuki, Yoshioka, Takamitsu, Hirata, Toshifumi, Aoki, Tadashi (1983) 13C NMR Signal Assignments of Herqueinone and Its Phenalenone Derivatives. Bulletin of the Chemical Society of Japan, 56 (12). 3661-3666 doi:10.1246/bcsj.56.3661
In(1983, December) Bulletin of the Chemical Society of Japan Vol. 56 (12) The Chemical Society of Japan

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Yoshioka, Takamitsu, Hirata, Toshifumi, Aoki, Tadashi, Suga, Takayuki (1982) Structural Studies on Herqueinone. The Configurations at C-4 of Herqueinone and at C-3 and C-4 of Dihydroherqueinone Monomethyl Ether. Bulletin of the Chemical Society of Japan, 55 (12). 3847-3851 doi:10.1246/bcsj.55.3847
Suga, Takayuki, Yoshioka, Takamitsu, Hirata, Toshifumi, Aoki, Tadashi (1981) THE C-4 CONFIGURATION AND13C NMR SIGNALS OF HERQUEINONE FROMPENICILLIUM HERQUEI. Chemistry Letters, 10 (8). 1063-1066 doi:10.1246/cl.1981.1063
Yoshioka, Takamitsu, Hirata, Toshifumi, Aoki, Tadashi, Suga, Takayuki (1981) THE STRUCTURAL STUDIES OF HERQUEINONE AND ITS DERIVATIVES.THE ABSOLUTE CONFIGURATION OF DIHYDROHERQUEINONE MONOMETHYL ETHER. Chemistry Letters, 10 (12). 1729-1732 doi:10.1246/cl.1981.1729
Suga, Takayuki, Ohta, Shinji, Aoki, Tadashi, Hirata, Toshifumi (1983) An X-Ray Crystallographic Study on the Absolute Configuration of Dihydroyashabushiketol and the Solvent-dependence of Its Optical Rotation. Bulletin of the Chemical Society of Japan, 56 (11). 3353-3357 doi:10.1246/bcsj.56.3353
Suga, Takayuki, Lee, Ym Sook, Hirata, Toshifumi (1983) The Hydroxylation of β-Terpineol and Its Acetate with the Cultured Cells ofNicotiana tabacum. Bulletin of the Chemical Society of Japan, 56 (3). 784-787 doi:10.1246/bcsj.56.784
Suga, Takayuki, Aoki, Tadashi, Hirata, Toshifumi, Aoki (née Sukemiya), Keiko, Asakawa, Yoshinori (1979) Structure of Alnustic Acid, a New Secodammarane-type Triterpenic Acid fromAlnus sieboldiana. Bulletin of the Chemical Society of Japan, 52 (6). 1698-1700 doi:10.1246/bcsj.52.1698
Hirata, Toshifumi, Aoki, Tadashi, Suga, Takayuki (1981) X-Ray Crystallographic Studies on the Structure of Alnuserrudiolone Isolated from the Male Flowers of Alnus serrulatoides. Bulletin of the Chemical Society of Japan, 54 (10). 3059-3063 doi:10.1246/bcsj.54.3059
Hirata, Toshifumi, Ideo, Reiko, Aoki, Tadashi, Suga, Takayuki (1982) The Structure of Alnuserrutriol, a New C31Dammarane-type Triterpenoid from the Male Flowers ofAlnus serrulatoides. Bulletin of the Chemical Society of Japan, 55 (2). 639-640 doi:10.1246/bcsj.55.639
Hirata, Toshifumi, Aoki, Tadashi, Hirano, Yoshio, Ito, Takashi, Suga, Takayuki (1981) The Biotransformation of Foreign Substrates by Tissue Cultures. I. The Hydroxylation of Linalool and Its Related Compounds with the Suspension Cells ofNicotiana tabacum. Bulletin of the Chemical Society of Japan, 54 (11). 3527-3529 doi:10.1246/bcsj.54.3527
Suga, Takayuki, Hirata, Toshifumi (1978) Biosynthesis of Aloenin inAloe arborescensvar.natalensis. Bulletin of the Chemical Society of Japan, 51 (3). 872-877 doi:10.1246/bcsj.51.872
Suga, Takayuki, Hirata, Toshifumi, Aoki, Tadashi (1982) An X-Ray Crystallographic Study oncis-transConfigurational Assignment to “cis-” and “trans-1,8-Terpins” and a Proposal of New Designation for Discriminating between the Configurational Isomers. Bulletin of the Chemical Society of Japan, 55 (3). 914-917 doi:10.1246/bcsj.55.914
 
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