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Effects of Methyl Substituents on the Activity and Enantioselectivity of Homobenzotetramisole-Based Catalysts in the Kinetic Resolution of Alcohols.
Adv Synth Catal. 2009 Oct 1;351(14-15):2525-2529. doi: 10.1002/adsc.200900383.
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Homobenzotetramisole-Catalyzed Kinetic Resolution of alpha-Aryl-, alpha-Aryloxy-, and alpha-Arylthioalkanoic Acids.
Adv Synth Catal. 2009;351(14):2301-2304. doi: 10.1002/adsc.200900451.
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Organocatalytic asymmetric addition of alcohols and thiols to activated electrophiles: efficient dynamic kinetic resolution and desymmetrization protocols.
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Homobenzotetramisole: an effective catalyst for kinetic resolution of aryl-cycloalkanols.
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The diverse chemistry of oxazol-5-(4H)-ones.
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Structural optimization of thiourea-based bifunctional organocatalysts for the highly enantioselective dynamic kinetic resolution of azlactones.
Org Biomol Chem. 2006 Dec 7;4(23):4319-30. doi: 10.1039/b607574f. Epub 2006 Nov 1.
7
Kinetic resolution of propargylic alcohols catalyzed by benzotetramisole.
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8
Kinetic resolution of 2-oxazolidinones via catalytic, enantioselective N-acylation.
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Asymmetric synthesis of protected arylglycines by rhodium-catalyzed addition of arylboronic acids to N-tert-butanesulfinyl imino esters.
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Benzotetramisole: a remarkably enantioselective acyl transfer catalyst.
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