Articles with "reduction substituted" as a keyword



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1,3,2‐Diazaphospholenes Catalyze the Conjugate Reduction of Substituted Acrylic Acids

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Published in 2020 at "ChemCatChem"

DOI: 10.1002/cctc.202000662

Abstract: The potent nucleophilicity and remarkably low basicity of 1,3,2‐diazaphospholenes (DAPs) is exploited in a catalytic, metal‐free 1,4‐reduction of free α,β‐unsaturated carboxylic acids. Notably, the reduction occurs without a prior deprotonation of the carboxylic acid moiety… read more here.

Keywords: reduction; reduction substituted; catalyze conjugate; diazaphospholenes catalyze ... See more keywords
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Reduction of 2-H-substituted pyrrolinium cations: the carbon-carbon single bond in air stable 2,2'-bipyrrolidines as a two-electron-source.

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Published in 2023 at "Chemical communications"

DOI: 10.1039/d3cc00891f

Abstract: Reduction of 2-H-substituted pyrrolinium cations via initially formed secondary radicals results in either dimerisation or H-abstracted products, while the outcome depends on the N-substituents. The resultant central carbon-carbon single bond in the dimerised 2,2'-bipyrrolidine derivatives… read more here.

Keywords: carbon; carbon carbon; substituted pyrrolinium; carbon single ... See more keywords
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Boron-Catalyzed Hydrogenative Reduction of Substituted Quinolines to Tetrahydroquinolines with Hydrosilanes

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Published in 2017 at "Synlett"

DOI: 10.1055/s-0036-1588442

Abstract: A metal-free procedure for the hydrogenative reduction of substituted N-heteroaromatics has been developed by using hydrosilanes as reducing agents. The optimized conditions were successfully applied to the reactions of quinolines, quinoxalines, and quinoline N-oxides. They… read more here.

Keywords: reduction; reduction substituted; substituted quinolines; boron catalyzed ... See more keywords
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MOF-808 as a Highly Active Catalyst for the Diastereoselective Reduction of Substituted Cyclohexanones

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Published in 2022 at "Molecules"

DOI: 10.3390/molecules27196315

Abstract: Zr-containing MOF-808 is an excellent heterogeneous catalyst for the diastereoselective Meerwein–Ponndorf–Verley reduction of substituted cyclohexanones. The presence of substituents at the 2 or 3 position of the cyclohexanone ring strongly drives the reaction towards the… read more here.

Keywords: mof 808; catalyst; catalyst diastereoselective; reduction substituted ... See more keywords