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Phytochemistry | 1988

A secoiridoid glucoside from Olea europaea

Hiroshi Kuwajima; Takeshi Uemura; Kiyokazu Takaishi; Kenichiro Inoue; Hiroyuki Inouyet

Abstract Besides two known glucosides, olcuropein and ligstroside, a new secoiridoid glucoside, oleuroside was isolated from Olea europaea and its structure


Phytochemistry | 1993

A quinol glucoside from Abeliophyllum distichum

Hiroshi Kuwajima; Mika Takahashi; Mami Ito; Wu Hua-Xin; Kiyokazu Takaishi; Kenichiro Inoue

Abstract Besides the known glucosides, calceolarioside D, verbascoside, cornoside, rutin and a cyclohexanone derivative, halleridone, a new quinol glucoside, ne


Phytochemistry | 1989

A secoiridoid glucoside from Ligustrum japonicum

Hiroshi Kuwajima; Katsunori Matsuuchi; Kiyokazu Takaishi; Kenichiro Inoue; Tetsuro Fujita; Hiroyuki Inouye

Abstract Besides several secoiridoid glucosides including 8-epikingiside, a new secoiridoid glucoside, methyl glucooleoside, was isolated from the ripe berries of Ligustrum japonicum and its structure elucidated.


Phytochemistry | 1989

Intermediacy of 6-hydroxyloganin in the ring cleavage course of loganin to secologanin

Kenichiro Inoue; Takao Tanahashi; Hiroyuki Inouye; Hiroshi Kuwajima; Kiyokazu Takaishi

Abstract A possible biosynthetic pathway from loganin to secologanin through ring cleavage of 6-hydroxyloganin was ruled out in feeding experiments in which Eustoma russellianum , Swertia japonica , Lonicera morrowii and Adina pilulifera were each presented with three C-6 and C-7 stereoisomers of 6-hydroxy [7- 2 H] loganin as well as [6,6,7,8- 2 H 4 ] - and [6,6,7,8 carbomethoxy- 2 H 7 ]-loganin. In an associated experiment, the reduction of the aldehyde group of secologanin leading to sweroside was shown to proceed by hydride ion attack from the si face.


Phytochemistry | 1993

A secoiridoid glucoside from Fraxinus insularis

Takao Tanahashi; Atsuko Shimada; Naotaka Nagakura; Kenichiro Inoue; Hiroshi Kuwajima; Kiyokazu Takaishi; Chen Cheng-Chang

Abstract A new secoiridoid glucoside, insularoside, was isolated from Fraxinus insularis . The structural elucidation of insularoside by spectroscopic and chemical studies is described. The biogenesis of this glucoside is also briefly discussed.


Phytochemistry | 1971

The content of coumarin analogues in red leaves of higher plants

Kiyokazu Takaishi

Abstract A remarkable amount of bound o -coumaric acid accompanied by a small amount of coumarin was isolated from red leaves of 20 plant species. It is noteworthy that the leaves of deeper red colour contain a higher amount of the bound o -coumaric acid. The amount of o -coumaric acid in one species reaches a maximum at the beginning of the red colouring, and decreases somewhat as the red colour deepens. This phenomena is interesting from biosynthetical point of view, since it has been shown that both coumarin and anthocyanins are synthesized through shikimic acid pathway. 1


Chemical & Pharmaceutical Bulletin | 1979

Plant Constituents biologically Active to Insects. I. Feeding Stimulants for the Larvae of the Yellow Butterfly, Eurema hecabe mandarina. (1)

Atsushi Numata; Kazuko Hokimoto; Atsuko Shimada; Hideo Yamaguchi; Kiyokazu Takaishi


Phytochemistry | 1996

An acetophenone glycoside from Exacum affine

Hiroshi Kuwajima; Naoka Shibano; Toshifumi Baba; Kiyokazu Takaishi; Kenichiro Inoue; Tetsuro Shingu


Applied Entomology and Zoology | 1985

Host-Plant Selection by the Yellow Butterfly Larvae, Eurema hecabe mandarine (Lepidoptera : Pieridae) : Attractants and Arrestants

Atsushi Numata; Hideo Yamaguchi; Kazuko Hokimoto; Masako Ohtani; Kiyokazu Takaishi


Chemical & Pharmaceutical Bulletin | 1977

Cyanogenic glycosides and glycosidase of Sorbus species.

Kiyokazu Takaishi; Hiroshi Kuwajima; Hiroko Hatano; Hiromi Go

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