Katsuo Asakura
Chiba University
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Featured researches published by Katsuo Asakura.
Biochemical Systematics and Ecology | 1999
Toshio Ando; Norio Saito; Fumi Tatsuzawa; Tomoko Kakefuda; Keiko Yamakage; Etsuko Ohtani; Maya Koshi-ishi; Yu Matsusake; Hisashi Kokubun; Hitoshi Watanabe; Tatsuya Tsukamoto; Yoshihiro Ueda; Goro Hashimoto; Eduardo Marchesi; Katsuo Asakura; Ritsuko Hara; Hiroko Seki
The flowers of 20 native taxa of Petunia (Solanaceae) were investigated by HPLC for the occurrence of anthocyanins. The investigation revealed the presence of at least 24 anthocyanins in their flowers, of which 18 known anthocyanins isolated from the flowers of P. exserta, P. guarapuavensis, P. integrifolia, P. occidentalis, and P. reitzii were fully identified by chemical and spectral methods to be 3-glucoside of delphinidin; 3-rutinosides of cyanidin, delphinidin, and petunidin; 3-rutinoside-5-glucosides, 3-trans and -cis-p-coumaroylrutinoside-5-glucosides, and 3-trans-caffeoylrutinoside-5-glucosides of delphinidin, petunidin, and malvidin; and 3-transcaffeoylglucosyl-trans-(caffeoyl or p-coumaroyl) rutinoside-5-glucosides of malvidin. Six novel anthocyanins were isolated from the flowers of P. occidentalis, and their structures were identified to be 3-glucosyl p-coumaroylrutinoside-5-glucosides and 3-glucosylcaffeoylrutinosides of petunidin and malvidin, and also 3-caffeoylglucosylcaffeoylrutinoside-5-glucoside and 3-caffeoylglucosyl p-coumaroylrutinoside-5-glucoside of petunidin. Out of the six pigments, petunidin 3-glucosyl p-coumaroylrutinoside-5-glucoside was unambiguously determined by spectral methods to be petunidin 3-O-[6-O-(4-O-(4-O-(β-d-glucopyranosyl)-trans-p-coumaroyl)-α-l-rhamnopyranosyl)-β-d-glucopyranoside]- 5-O-[β-d-glucopyranoside]. The 20 native taxa of Petunia could be placed into four groups (A, B, C, and D) with one further into five subgroups (D1–D5) regarding their constituents and contents of major anthocyanins and also their pigment biosynthesis with respect to the blocks or inhibitors of the hydroxylation, glucosylation, and acylation reactions in them. The use of anthocyanins as taxonomic markers in the genus Petunia is discussed in relation to the flower colour and possible pollination vectors.
Tetrahedron Letters | 1996
Tsuneo Imamoto; Katsuo Asakura; Hideyuki Tsuruta; Kuniyuki Kishikawa; Kentaro Yamaguchi
Abstract Syntheses, structural characterizations, and reactions of tricyclohexylphosphine-trifluoromethanesulfonyloxyborane and tricyclohexylphosphine-bis(trifluoromethanesulfonyloxy)-borane are described.
Phytochemistry | 1999
Fumi Tatsuzawa; Toshio Ando; Norio Saito; Kyoko Yoda; Hisashi Kokubun; Hitoshi Watanabe; Goro Hashimoto; Katsuo Asakura; Ritsuko Hara; Hiroko Seki
Abstract A new acylated anthocyanin was isolated from a strain of Petunia integrifolia subsp. inflata with dusky violet flowers (B1204d), and identified as malvidin 3- O -[6- O -(4- O -(4- O -(6- O -( trans -caffeoyl)- β - d -glucopyranosyl)- trans - p -coumaroyl)- α - l -rhamnopyranosyl)- β - d -glucopyranoside] as a major pigment. Also, two known pigments were found in these flowers, and determined to be malvidin 3-caffeoylrutinoside and 3- p -coumaroylrutinoside.
Bulletin of the Chemical Society of Japan | 2001
Katsuo Asakura; Tsuneo Imamoto
Chemistry Letters | 2005
Tomomitsu Kurimoto; Katsuo Asakura; Chiharu Yamasaki; Nobuaki Nemoto
Archive | 2003
Katsuo Asakura; Tomomitsu Kurimoto; Nobuaki Nemoto; Chiharu Yamazaki; 千春 山崎; 克夫 朝倉; 智充 栗本; 暢明 根本
Chemistry Letters | 2000
Katsuo Asakura; Kentaro Yamaguchi; Tsuneo Imamoto
Archive | 2005
Katsuo Asakura; Nobuaki Nemoto; Yuichi Shimoikeda; 下池田勇一; 朝倉克夫; 根本暢明
Chemistry Letters | 2005
Katsuo Asakura; Tomomitsu Kurimoto; Nobuaki Nemoto
Archive | 2004
Katsuo Asakura; Tomomitsu Kurimoto; Nobuaki Nemoto; Chiharu Yamasaki