Tuesday, December 30, 2014

Direct amidation of the phenylalanine moiety in short peptides via Pd-catalyzed C–H activation/C–N formation

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DOI:  10.1039/C4QO00282B
Monday, December 29, 2014

Cobalt(III)-Catalyzed Synthesis of Indazoles and Furans by C–H Bond Functionalization/Addition/Cyclization Cascades

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DOI:  10.1021/ja5116452

Copper-Catalyzed C–H Functionalization Reactions: Efficient Synthesis of Heterocycles

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DOI:  10.1021/cr500410y

Palladium-Catalyzed ortho-Sulfonylation of 2-Aryloxypyridines and Subsequent Formation of ortho-Sulfonylated Phenols

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DOI:  10.1021/jo5026095

Synthesis of Benzofused Five-Ring Sultams via Rh-Catalyzed C–H Olefination Directed by an N-Ac-Substituted Sulfonamide Group

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DOI:  10.1021/jo502224d

Silver-Catalyzed C(sp2)–H Functionalization/C–O Cyclization Reaction at Room Temperature

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DOI:  10.1021/jo5024238

RhIII-Catalyzed Redox-Neutral C–H Activation of Pyrazolones: An Economical Approach for the Synthesis of N-Substituted Indoles

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DOI:  10.1021/ol503404p

Copper-Mediated Trifluoromethylation Using Phenyl Trifluoromethyl Sulfoxide

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DOI:  10.1021/ol5034018
Thursday, December 25, 2014

From Anilines to Isatins: Oxidative Palladium-Catalyzed Double Carbonylation of C[BOND]H Bonds

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DOI: 10.1002/anie.201410321
Tuesday, December 23, 2014

Palladium(ii)-catalyzed meta-selective direct arylation of O-β-naphthyl carbamate

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DOI:  10.1039/C4CC07997C
Monday, December 22, 2014

Pd-Catalyzed Monoselective ortho-C–H Alkylation of N-Quinolyl Benzamides: Evidence for Stereoretentive Coupling of Secondary Alkyl Iodides

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DOI:  10.1021/ja511557h

Palladium-Catalyzed ortho-Selective C–H Fluorination of Oxalyl Amide-Protected Benzylamines

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DOI:  10.1021/jo502365b

Rhodium(III)-Catalyzed Hydrazine-Directed C–H Activation for Indole Synthesis: Mechanism and Role of Internal Oxidant Probed by DFT Studies

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DOI:  10.1021/om501130c

Computational Mechanistic Study of Palladium(II)-Catalyzed Carboxyalkynylation of an Olefin Using an Iodine(III) Oxidant Reagent

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DOI:  10.1021/om5011758

Pd-Catalyzed Dehydrogenative Aryl–Aryl Bond Formation via Double C(sp2)–H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles

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DOI:  10.1021/ol503442n