Abstract
Shengrong Chen, Jinghong Wu, Hongya Zhu, Ping Guo, 耶芸 魏, X X Yang
Abstract
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Institutions
Provenance
crossref
Confidence 100%
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Site-selective C-H functionalization to access the arene backbone of indoles and quinolines
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Transition metal-catalyzed C–H functionalizations of indoles
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Pd(II)-Catalyzed meta-C–H Olefination, Arylation, and Acetoxylation of Indolines Using a U-Shaped Template
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Total Synthesis of Verruculogen and Fumitremorgin A Enabled by Ligand-Controlled C–H Borylation
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openalex
Confidence 95%
datacite
Confidence 0%
Cu-Catalyzed Direct C6-Arylation of Indoles
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Remote C6-Selective Ruthenium-Catalyzed C–H Alkylation of Indole Derivatives via σ-Activation
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Catalytic C6 Functionalization of 2,3-Disubstituted Indoles by Scandium Triflate
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Remote Stereocontrol in the C6-Functionalization of Indoles via Synergistic Ion-Pair Catalysis
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meta-C–H Arylation and Alkylation of Benzylsulfonamide Enabled by a Palladium(II)/Isoquinoline Catalyst
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Ligand-Enabled Auxiliary-Free meta-C–H Arylation of Phenylacetic Acids
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Differentiation and functionalization of remote C–H bonds in adjacent positions
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Entry to 1,2,3,4-Tetrasubstituted Arenes through Addressing the “Meta Constraint” in the Palladium/Norbornene Catalysis
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Electrically driven directional motion of a four-wheeled molecule on a metal surface
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Complementary site-selectivity in arene functionalization enabled by overcoming the orthoconstraint in palladium/norbornene catalysis
10.1038/s41557-018-0074-z · doi-reference
From Pd(OAc)2 to Chiral Catalysts: The Discovery and Development of Bifunctional Mono-N-Protected Amino Acid Ligands for Diverse C–H Functionalization Reactions
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Palladium (II)-Catalyzed C–H Activation with Bifunctional Ligands: From Curiosity to Industrialization
10.1002/anie.202400509 · doi-reference
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10.1002/anie.202011901 · doi-reference
Palladium(II)-Catalyzed Direct C7-Acyloxylation of Indoles
10.1021/acs.orglett.5c04739 · doi-reference
meta-C–H functionalization of phenylethyl and benzylic alcohol derivatives via Pd/NBE relay catalysis
10.1039/d4sc03802a · doi-reference
Differentiation and functionalization of remote C–H bonds in adjacent positions
10.1038/s41557-020-0424-5 · doi-reference
Palladium-Catalyzed meta-C–H Functionalization of Masked Aromatic Aldehydes
10.1021/acscatal.8b01599 · doi-reference
Ligand-Promoted meta-C–H Functionalization of Benzylamines
10.1002/anie.201701803 · doi-reference
Ligand-Enabled Auxiliary-Free meta-C–H Arylation of Phenylacetic Acids
10.1002/anie.201702686 · doi-reference
meta-C–H Arylation and Alkylation of Benzylsulfonamide Enabled by a Palladium(II)/Isoquinoline Catalyst
10.1002/anie.201704411 · doi-reference
Ligand Promoted meta-C–H Chlorination of Anilines and Phenols
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Ligand-Promoted Meta-C–H Arylation of Anilines, Phenols, and Heterocycles
10.1021/jacs.6b04966 · doi-reference
Ligand-Promoted meta-C–H Amination and Alkynylation
10.1021/jacs.6b08942 · doi-reference
Ligand-Enabled meta-Selective C–H Arylation of Nosyl-Protected Phenethylamines, Benzylamines, and 2-Aryl Anilines
10.1021/jacs.6b11097 · doi-reference
Ligand-Enabled Meta-C–H Alkylation and Arylation Using a Modified Norbornene
10.1021/jacs.5b08914 · doi-reference
Ligand-enabled meta-C-H activation using a transient mediator
10.1038/nature14214 · doi-reference
Regioselective one-step C2-H methylation of free (N-H) indoles enabled by Pd(II)/norbornene cooperative catalysis
10.1039/d5qo00869g · doi-reference
Triple cross-electrophile coupling enabled by palladium/norbornene cooperative catalysis
10.1126/sciadv.adu4573 · doi-reference
Catellani Reaction: An Enabling Technology for Vicinal Functionalization of Aryl Halides by Palladium(0)/Norbornene Cooperative Catalysis
10.1002/cjoc.202000600 · doi-reference
Palladium(II)-Initiated Catellani-Type Reactions
10.1002/anie.201813491 · doi-reference
Structurally Modified Norbornenes: A Key Factor to Modulate Reaction Selectivity in the Palladium/Norbornene Cooperative Catalysis
10.1021/jacs.0c09193 · doi-reference
Palladium/Norbornene Cooperative Catalysis
10.1021/acs.chemrev.9b00079 · doi-reference
Pd/Norbornene: A Winning Combination for Selective Aromatic Functionalization via C–H Bond Activation
10.1021/acs.accounts.6b00165 · doi-reference
Dispersion-controlled C6-selective C–H borylation of indoles
10.1039/d5cc01554e · doi-reference
Remote Stereocontrol in the C6-Functionalization of Indoles via Synergistic Ion-Pair Catalysis
10.1021/acscatal.5c00780 · doi-reference
Catalytic C6 Functionalization of 2,3-Disubstituted Indoles by Scandium Triflate
10.1021/jo402511b · doi-reference
Chiral Phosphoric Acid-Catalyzed C6 Functionalization of 2,3-Disubstituted Indoles for Synthesis of Heterotriarylmethanes
10.1021/acs.orglett.0c04002 · doi-reference
Remote C6-Selective Ruthenium-Catalyzed C–H Alkylation of Indole Derivatives via σ-Activation
10.1021/acscatal.7b00038 · doi-reference
Cu-Catalyzed Direct C6-Arylation of Indoles
10.1021/jacs.6b05777 · doi-reference
Total Synthesis of Verruculogen and Fumitremorgin A Enabled by Ligand-Controlled C–H Borylation
10.1021/jacs.5b07154 · doi-reference
Pd(II)-Catalyzed meta-C–H Olefination, Arylation, and Acetoxylation of Indolines Using a U-Shaped Template
10.1021/ja505737x · doi-reference
Transition metal-catalyzed C–H functionalizations of indoles
10.1039/d1nj01696b · doi-reference
Site-selective C-H functionalization to access the arene backbone of indoles and quinolines
10.1039/d0cs00334d · doi-reference
From C4 to C7: Innovative Strategies for Site-Selective Functionalization of Indole C–H Bonds
10.1021/acs.accounts.0c00888 · doi-reference
Beyond C2 and C3: Transition-Metal-Catalyzed C–H Functionalization of Indole
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