H
Huanfeng Jiang
Researcher at South China University of Technology
Publications - 606
Citations - 13566
Huanfeng Jiang is an academic researcher from South China University of Technology. The author has contributed to research in topics: Catalysis & Palladium. The author has an hindex of 55, co-authored 543 publications receiving 10971 citations. Previous affiliations of Huanfeng Jiang include Chinese Academy of Sciences & University of Rennes.
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Palladium-assisted multicomponent cyclization of aromatic aldehydes, arylamines and terminal olefins under molecular oxygen: an assembly of 1,4-dihydropyridines
TL;DR: P palladium-assisted one-pot three-component reactions of aldehydes, amines and olefins proceeded smoothly to give 2,6-unsubstituted 1,4-dihydropyridines (1,4 -DHPs) using molecular oxygen as a sole oxidant.
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Practical Iridium-Catalyzed Direct α-arylation of N-heteroarenes with (Hetero)arylboronic Acids by H2O-Mediated H2 Evolution
TL;DR: By a H2O-mediated H2-evolution cross-coupling strategy, a new iridium(III)-catalyzed facile method to direct α-arylation of N-heteroarenes with both aryl and heteroaryl boronic acids is reported, proceeding with broad substrate scope and excellent functional compatibility.
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Solvent-free heterogeneous organocatalysis : stereoselective isomerization of α,β-ynones to (E,E)-α,β-γ,δ -dienones catalyzed by polymer-supported tertiaryphosphines
TL;DR: Stereoselective isomerization of α,β-ynones was catalyzed by polymer-supported tertiaryphosphines under solvent-free conditions as mentioned in this paper, with up to 93% isolated yields when JJ-TPP was employed.
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Rh(II)-catalyzed formation and rearrangement of trifluoroacetyl-containing sulfur ylides
TL;DR: In this article, a facile, convenient, efficient, and high yielding Rh(II)-catalyzed formation and rearrangement of trifluoroacetyl-containing sulfur ylides is reported.
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Gold-Catalyzed Ring Expansion of Enyne-Lactone: Generation and Transformation of 2-Oxoninonium.
TL;DR: An efficient gold-catalyzed ring-expansion reaction of enyne-lactones to form 2-oxoninonium intermediates is reported and could undergo further 6π electrocyclization and aromatization reaction to produce different aromatic compounds.