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Thiopyrans and Their Benzo Derivatives
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The article was published on 2020-01-01. It has received 1 citations till now. The article focuses on the topics: Ring (chemistry) & Section (typography).read more
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Bis(2-aminobenzoimidazole)-Organocatalyzed Asymmetric Alkylation of Activated Methylene Compounds with Benzylic and Allylic Alcohols
TL;DR: In this paper, the first organocatalyzed asymmetric alkylation of activated methylene compounds using benzylic and allylic alcohols as alkylating agents through dual hydrogen bond activation in an SN1-type reaction is reported.
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Catalytic Asymmetric Oxidative α-C-H N,O-Ketalization of Ketones by Chiral Primary Amine.
TL;DR: A highly enantioselective primary amine catalyzed α,α-bis-functionalization of β-ketocarbonyls and cyclohexanones is described, which employs N-hydroxycarbamates as both nitrogen and oxygen sources under aerobic oxidative conditions to furnish chiral N,O-ketals with high yields and enantiOSElectivities.
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Photo-polymerized epoxy primer for adhesion improvement at thermoplastics/metallic wires interfaces
TL;DR: In this paper, an innovative fast-curing coupling method using a UV-curable epoxy primer based on a cycloaliphatic di-epoxide resin to bond metallic wires and a thermoplastic polyurethane matrix was reported.
Journal ArticleDOI
Bridging Rhodium–Iron Borataaminocarbyne Complexes Formed by Intramolecular Isonitrile–Borane Coordination
TL;DR: In this article, a borataaminocarbyne ligand with single bonds between carbon and nitrogen and between nitrogen and boron was described, and the CNRBR3 unit was best described as a BORATAMINOCARBYNE ligand, which is doubly bound to iron and single bound to rhodium.
Journal ArticleDOI
One-Pot Access to a Library of Dispiro Oxindole-pyrrolidine/pyrrolothiazole-thiochromane Hybrids via Three-Component 1,3-Dipolar Cycloaddition Reactions.
TL;DR: This experimentally simple protocol provides good yields of structurally complex, biologically relevant heterocycles in a single operation by the three-component 1,3-dipolar cycloaddition of azomethine ylides generated in situ from the condensation of isatins and secondary amino acids.