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1
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…
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Keywords:
reduction;
reduction substituted;
catalyze conjugate;
diazaphospholenes catalyze ... See more keywords
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2
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…
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Keywords:
carbon;
carbon carbon;
substituted pyrrolinium;
carbon single ... See more keywords
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0
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…
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Keywords:
reduction;
reduction substituted;
substituted quinolines;
boron catalyzed ... See more keywords
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1
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…
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Keywords:
mof 808;
catalyst;
catalyst diastereoselective;
reduction substituted ... See more keywords