scispace - formally typeset
T

Takashi Ooi

Researcher at University of Tokushima

Publications -  18
Citations -  379

Takashi Ooi is an academic researcher from University of Tokushima. The author has contributed to research in topics: Absolute configuration & Diterpene. The author has an hindex of 11, co-authored 18 publications receiving 357 citations. Previous affiliations of Takashi Ooi include University of Tsukuba.

Papers
More filters
Journal ArticleDOI

Cyanoviridin RR, a toxin from the cyanobacterium (blue-green alga) microcystis viridis

TL;DR: A toxin, named as cyanoviridin RR, has been isolated from the cyanobacterium Microcystis viridis and the structure of the toxin has been determined by modern NMR techniques such as the HMBC spectrum.
Journal ArticleDOI

The Modified Mosher’s Method and the Sulfoximine Method

TL;DR: In this article, the modified Mosher's method is applied to a variety of natural products possessing a secondary alcohol for determining their absolute configuration, and the method is described in detail.
Journal ArticleDOI

Three new polyketide-terpenoid hybrids from Penicillium sp.

TL;DR: Three novel hybrid polyketide-terpenoid metabolites were isolated from a Penicillium minioluteum strain and the proposed biosynthetic pathway including a unique retro-Claisen migration of methyl carbonate correlates the three compounds with berkeleydione and berkeleytrione.
Journal ArticleDOI

Isolation and absolute configuration determination of aliphatic sulfates as the Daphnia kairomones inducing morphological defense of a phytoplankton.

TL;DR: In this article, 2,6-dimethylheptyl sulfate and 6-methyl octyl sulfates were isolated from Daphnia pulex as kairomones that induced morphological defense of a freshwater phytoplankton Scenedesmus gutwinskii var. heterospina.
Journal ArticleDOI

A diterpenoid phenalenone from Salvia miltiorrhiza

TL;DR: In this paper, a phenalenone isolated from Salvia miltiorrhiza was identified as 9-isopropyl-2,2,5-trimethyl-8H-paleno[1,9bc]furan8-one, a compound which had been artificially prepared by rearrangement of taxoquinone and other royleanones.