scispace - formally typeset
N

Noriyuki Kogure

Researcher at Chiba University

Publications -  110
Citations -  2203

Noriyuki Kogure is an academic researcher from Chiba University. The author has contributed to research in topics: Indole alkaloid & Total synthesis. The author has an hindex of 25, co-authored 110 publications receiving 1974 citations. Previous affiliations of Noriyuki Kogure include University of Santo Tomas & Chiba Institute of Science.

Papers
More filters
Journal ArticleDOI

Two new tryptamine-derived alkaloids from Chimonanthus praecox f. concolor

TL;DR: A pyrrolidinoindoline-type alkaloid, CPC-1, and a tryptamine-derived dimeric alkyline, called CPC-2, were isolated from the seeds and rinds of Chimonanthus praecox f. concolor as mentioned in this paper.
Journal ArticleDOI

Metabolomics-oriented isolation and structure elucidation of 37 compounds including two anthocyanins from Arabidopsis thaliana.

TL;DR: This study isolated metabolites of Arabidopsis in a relatively non-targeted way, aiming at the construction of metabolite standards and chemotaxonomic comparison.
Journal ArticleDOI

Isolation of gelsedine-type indole alkaloids from Gelsemium elegans and evaluation of the cytotoxic activity of gelsemium alkaloids for A431 epidermoid carcinoma cells.

TL;DR: Four new gelsedine-type indole alkaloids were isolated from the leaves of Gelsemium elegans, together with 11 known alkaloid structures determined as 14-acetoxygelsenicine, which showed potent cytotoxic effects.
Journal ArticleDOI

New lycorine-type alkaloid from Lycoris traubii and evaluation of antitrypanosomal and antimalarial activities of lycorine derivatives.

TL;DR: A new lycorine derivative LT1 was isolated from the aerial part and bulbs of Lycoris traubii Hayward and established by spectroscopic analysis and semi-synthesis to be 1-O-(3'S)-hydroxybutanoyllycorine, which showed significant activity against P. falciparum in an in vitro experiment.
Journal ArticleDOI

Asymmetric Total Synthesis of a Pentacyclic Lycopodium Alkaloid: Huperzine‐Q

TL;DR: Right on Q: the first asymmetric total synthesis of (-)-huperzine-Q, which possesses six stereogenic centers and a spiroaminal moiety, has been achieved in 19 steps and 16.4 % overall yield.