Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies. - Wikidata - wikimedia - TriplyDB

Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.

Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.

http://www.wikidata.org/entity/Q34962552

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Recent advances in homogeneous nickel catalysis Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF The role of aryne distortions, steric effects, and charges in regioselectivities of aryne reactions A modular, air-stable nickel precatalyst.Nickel-catalysed Suzuki-Miyaura coupling of amides.Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling in a Green Alcohol Solvent for an Undergraduate Organic Chemistry Laboratory New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles.Conversion of amides to esters by the nickel-catalysed activation of amide C-N bonds.Nickel-catalyzed amination of aryl sulfamates and carbamates using an air-stable precatalyst Iron-catalyzed alkylations of aryl sulfamates and carbamates.Nanonickel-catalyzed Suzuki-Miyaura cross-couplings in water.Mechanistic studies of copper(I)-catalyzed 1,3-halogen migration Nickel-catalyzed Suzuki-Miyaura couplings in green solvents.Nickel-Catalyzed Cross-Coupling Reactions of Unreactive Phenolic Electrophiles via C-O Bond Activation.Pd(II)-Catalyzed C3-Selective Arylation of Pyridine with (Hetero)arenes.Synthetic studies on pseudo-dimeric Lycopodium alkaloids: total synthesis of complanadine B.Nickel-mediated hydrogenolysis of C-O bonds of aryl ethers: what is the source of the hydrogen?Pd-catalyzed Suzuki-Miyaura cross-coupling reactions between sulfamates and potassium Boc-protected aminomethyltrifluoroborates.Palladium-catalyzed Suzuki-Miyaura coupling of aryl sulfamates with arylboronic acids.Mechanistic Study of an Improved Ni Precatalyst for Suzuki-Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species.Comparison of dppf-Supported Nickel Precatalysts for the Suzuki-Miyaura Reaction: The Observation and Activity of Nickel(I).Mechanism and Origins of Ligand-Controlled Stereoselectivity of Ni-Catalyzed Suzuki-Miyaura Coupling with Benzylic Esters: A Computational Study.Ruthenium-catalyzed olefinic C-H alkenylation of enol-carbamates: highly stereo-selective synthesis of (Z,Z) and (Z,E)-butadienes.Ligand-free, palladacycle-facilitated Suzuki coupling of hindered 2-arylbenzothiazole derivatives yields potent and selective COX-2 inhibitors.Efficient cross-coupling of aryl/alkenyl triflates with acyclic secondary alkylboronic acids.Why different ligands can control stereochemistry selectivity of Ni-catalyzed Suzuki-Miyaura cross-coupling of benzylic carbamates with arylboronic esters: a mechanistic study.Efficient Ni-catalyzed conversion of phenols protected with 2,4,6-trichloro-1,3,5-triazine (TCT) to olefins.Pd-Catalyzed Suzuki-Miyaura and Hiyama-Denmark Couplings of Aryl Sulfamates.Ni(ii)-catalyzed asymmetric addition of arylboronic acids to cyclic imines.Base-promoted coupling of carbon dioxide, amines, and diaryliodonium salts: a phosgene- and metal-free route to O-aryl carbamates.How and Why Does Ni(0) Promote Smooth Etheric C-O Bond Cleavage and C-C Bond Formation? A Theoretical Study.Synthesis of Biaryls through Nickel-Catalyzed Suzuki-Miyaura Coupling of Amides by Carbon-Nitrogen Bond Cleavage.Modular Construction of Fluoroarenes from a New Difluorinated Building Block by Cross-Coupling/Electrocyclisation/Dehydrofluorination Reactions.C-H arylation and alkenylation of imidazoles by nickel catalysis: solvent-accelerated imidazole C-H activation.Aryl Ether as a Negishi Coupling Partner: An Approach for Constructing CC Bonds under Mild Conditions

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P2860

Suzuki-Miyaura cross-coupling of aryl carbamates and sulfamates: experimental and computational studies.

http://www.wikidata.org/entity/Q34962552

description

2011 nî lūn-bûn

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2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2011 թվականի ապրիլին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Journal of the American Chemical Society

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Suzuki-Miyaura cross-coupling ...... tal and computational studies.

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Amanda L Silberstein

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Anna Komaromi

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Aurora Antoft-Finch

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Kyle W Quasdorf

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Neil K Garg

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Stephen D Ramgren

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Tom Blackburn

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Victor Snieckus

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P2860

Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

Aryl-aryl bond formation one century after the discovery of the Ullmann reaction

Flurbiprofen in the symptomatic management of rheumatoid arthritis: a valuable alternative

DirectedorthoMetalation−Boronation and Suzuki−Miyaura Cross Coupling of Pyridine Derivatives: A One-Pot Protocol to Substituted Azabiaryls#

Nickel-catalyzed C-O activation of phenol derivatives with potassium heteroaryltrifluoroborates.

Palladium-catalyzed coupling of ammonia with aryl chlorides, bromides, iodides, and sulfonates: a general method for the preparation of primary arylamines.

Pd-catalyzed cross-coupling reactions of amides and aryl mesylates.

The Newman-Kwart rearrangement of O-aryl thiocarbamates: substantial reduction in reaction temperatures through palladium catalysis.

Kumada coupling of aryl and vinyl tosylates under mild conditions.

Nickel-catalyzed cross-couplings involving carbon-oxygen bonds

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6352-6363

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10.1021/JA200398C

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16

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21456551

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