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Colin B. Rogers

Researcher at University of Durban-Westville

Publications -  26
Citations -  610

Colin B. Rogers is an academic researcher from University of Durban-Westville. The author has contributed to research in topics: Combretaceae & Cladosporium cucumerinum. The author has an hindex of 15, co-authored 26 publications receiving 577 citations. Previous affiliations of Colin B. Rogers include University of KwaZulu-Natal.

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Isolation, Synthesis, and Antiplatelet Aggregation Activity of Resveratrol 3-O-β-d-Glucopyranoside and Related Compounds†

TL;DR: The synthesis of 1, related hydroxystilbenes, and their glucosides has been undertaken to provide larger quantities, for further biological evaluation, and has been accomplished via Wittig reactions followed by glucosylation under phase transfer catalysis.
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Typhaphthalide and typharin, two phenolic compounds from Typha capensis.

TL;DR: Two new phenolics, named typhaphthalide (a benzylphthalide) and typharin (an isocoumarin) plus sitosterol were isolated and identified from the hexane extract of the rhizomes of Typha capensis.
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Novel Prenylated Xanthones from Garcinia gerrardii HARVEY

TL;DR: In this paper, three prenylated xanthones, 1−3, have been isolated from the root bark of Garcinia gerrardii and structure elucidation was achieved by a combination of one-and two-dimensional NMR spectroscopic techniques, including long-range HETCOR, mass spectroscopy, and chemical methods.
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Prenylated xanthones fromGarcinia livingstonei

TL;DR: Five prenylated xanthones have been isolated from the root bark of Garcinia livingstonei of which four are novel natural products, and two compounds are fungicidal against Cladosporium cucumerinum, whereas a third shows growth inhibitory activity against human colon carcinoma cell lines.
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The structure of imberbic acid, A 1α-hydroxy pentacyclic triterpenoid from Combretum imberbe

TL;DR: A new 1α-hydroxy pentacyclic triterpenoid acid, imberbic acid, has been isolated from the leaves of Combretum imberbe and its structure established as 1α,3β-dihydroxyolean-12-en-29-oic acid by chemical and spectral analysis as mentioned in this paper.