H
Henok H. Kinfe
Researcher at University of Johannesburg
Publications - 73
Citations - 623
Henok H. Kinfe is an academic researcher from University of Johannesburg. The author has contributed to research in topics: Catalysis & Glycal. The author has an hindex of 14, co-authored 72 publications receiving 504 citations. Previous affiliations of Henok H. Kinfe include Council of Scientific and Industrial Research & University of Cape Town.
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Journal ArticleDOI
Synthesis of structures corresponding to the capsular polysaccharide of Neisseria meningitidis group A
Rikard Slättegård,Peter Teodorovic,Henok H. Kinfe,Neil Ravenscroft,David W. Gammon,Stefan Oscarson +5 more
TL;DR: Four differently substituted trimers of the CPS repeating unit have been synthesised in order to investigate the dependence on oligosaccharide size, acetylation and mode of phosphorylation of glycoconjugate vaccines against Neisseria meningitidis group A.
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Efficient tetrahydropyranyl and tetrahydrofuranyl protection/deprotection of alcohols and phenols with Al(OTf)3 as catalyst
TL;DR: In this article, a simple and efficient method for the conversion of alcohols and phenols into their corresponding THP and THF ethers at room temperature has been developed using 1 ǫ% aluminium triflate as catalyst.
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Versatility of glycals in synthetic organic chemistry: coupling reactions, diversity oriented synthesis and natural product synthesis
TL;DR: This review summarizes the literature on the different transformations of the endo glycals into biologically relevant compounds as well as on the use of glycals as chiral building blocks for the synthesis of various natural products such as aspicilin, reblastatin, diospongins, decytospolides, osmundalactones, paclitaxel, isatisine, d-fagomine, and spliceostatin, reported post 2014.
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A New Catalytic Route for the Oxidative Halogenation of Cyclic Enol Ethers using Tungstate Exchanged on Takovite
Bert F. Sels,Pieter Levecque,Roald Brosius,Dirk De Vos,Pierre Jacobs,David W. Gammon,Henok H. Kinfe +6 more
TL;DR: In this paper, an efficient and benign method for the regio-and stereoselective synthesis of halohydrins and β-halo ethers from dihydropyrans, dihydrofurans and anhydro sugars in the presence of a halide salt and hydrogen peroxide is presented with tungstate-exchanged takovite as oxidation catalyst.
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Naturally Occurring Homoisoflavonoids: Phytochemistry, Biological Activities, and Synthesis (Part II):
TL;DR: This review takes note of the recent revision of plant families that were known to contain HIFs that have now been merged into one big family, Asparagaceae, and contains their structures, biological sources, plant parts they are obtained from, and, if reported, their optical rotations and melting points.