K
Kenji Mishiro
Researcher at Kanazawa University
Publications - 42
Citations - 597
Kenji Mishiro is an academic researcher from Kanazawa University. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 11, co-authored 31 publications receiving 453 citations. Previous affiliations of Kenji Mishiro include Kyoto University & University of Manchester.
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Journal ArticleDOI
Selecting reactions and reactants using a switchable rotaxane organocatalyst with two different active sites
Jack Beswick,Victor Blanco,Guillaume De Bo,David A. Leigh,Urszula Lewandowska,Bartosz Lewandowski,Kenji Mishiro +6 more
TL;DR: The activation mode of a rotaxane-based organocatalyst with both secondary amine and squaramide catalytic units can be switched with acid or base, affording different products from a mixture of three building blocks.
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Functional group tolerance in organocatalytic regioselective acylation of carbohydrates.
TL;DR: Functional group tolerance in the regioselective acylation catalyzed by 1 was found to be high and the results confirmed that mono- and disaccaharides derived from alpha-amino acids, cinnamic acid, and gallic acid can be converted to functionalized acid anhydrides with similar properties.
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Total Synthesis of Ellagitannins through Regioselective Sequential Functionalization of Unprotected Glucose
TL;DR: Short total syntheses of natural glycosides (ellagitannins) were performed through sequential and regioselective functionalization of the hydroxy groups of unprotected glucose to achieve β-selective glycosidation of a gallic acid derivative.
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Regioselective Diversification of a Cardiac Glycoside, Lanatoside C, by Organocatalysis
TL;DR: Diverse regioselective introduction of acyl groups among eight free hydroxy groups of lanatoside C was achieved.
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Perfectly Regioselective and Sequential Protection of Glucopyranosides
TL;DR: In this article, a perfectly regioselective and sequential method for the preparation of orthogonally protected glucopyranosides has been developed, and an acyl group was introduced at C(4)-OH by organocatalysis with >99 % regiuoselectivity.