Raji Chem World
Save the World By Green Chemistry
Wednesday, December 13, 2017
Sustainable Conversion of Carbon Dioxide: An Integrated Review of Catalysis and Life Cycle Assessment
Catalytic Organic Reactions in Water toward Sustainable Society
Redox-Tag Processes: Intramolecular Electron Transfer and Its Broad Relationship to Redox Reactions in General
Sunday, November 26, 2017
Catalyst-controlled oligomerization for the collective synthesis of polypyrroloindoline natural products
Recent advances in catalytic C−H borylation reactions
Thursday, November 23, 2017
Group 6 Dihapto-Coordinate Dearomatization Agents for Organic Synthesis
Mechanism of Rhodium-Catalyzed C–H Functionalization: Advances in Theoretical Investigation
Achieving Molecular Complexity via Stereoselective Multiple Domino Reactions Promoted by a Secondary Amine Organocatalyst
Experimental–Computational Synergy for Selective Pd(II)-Catalyzed C–H Activation of Aryl and Alkyl Groups
DOI:
10.1021/acs.accounts.7b00440
Speciation in iron epoxidation catalysis: A perspective on the discovery and role of non-heme iron(III)-hydroperoxo species in iron-catalyzed oxidation reactions
Piano-stool N-heterocyclic carbene iron complexes: Synthesis, reactivity and catalytic applications
Monday, November 20, 2017
Toward Green Acylation of (Hetero)arenes: Palladium-Catalyzed Carbonylation of Olefins to Ketones
DOI:
10.1021/acscentsci.7b00368
Building Diversity in ortho-Substituted s-Aryltetrazines By Tuning N-Directed Palladium C–H Halogenation: Unsymmetrical Polyhalogenated and Biphenyl s-Aryltetrazines
DOI:
10.1021/acscatal.7b03186
Ruthenium-Catalyzed C–H Benzoxylation of tert-Benzamides with Aromatic Acids by Weak Coordination
DOI:
10.1021/acs.joc.7b02495
Rh(III)-Catalyzed Direct ortho-Chalcogenation of Phenols and Anilines
Synthesis and Reactivity of Model Intermediates Proposed for the Pd-Catalyzed Remote C–H Functionalization of N-(2-Haloaryl)acrylamides
DOI:
10.1021/acs.organomet.7b00702
Rhodium Complexes of 2,6-Bis(dialkylphosphinomethyl)pyridines: Improved C–H Activation, Expanded Reaction Scope, and Catalytic Direct Arylation
DOI:
10.1021/acs.organomet.7b00532
Copper-Mediated C–X Functionalization of Aryl Halides
DOI:
10.1021/acs.oprd.7b00285
OMS-2/H2O2/Dimethyl Carbonate: An Environmentally-Friendly Heterogeneous Catalytic System for the Oxidative Synthesis of Benzoxazoles at Room Temperature
DOI:
10.1021/acs.oprd.7b00315
Copper-Catalyzed Dehydrogenative Formal [4 + 2] and [3 + 2] Cycloadditions of Methylnaphthalenes and Electron-Deficient Alkenes
DOI:
10.1021/acs.orglett.7b03194
Mechanochemical Ruthenium-Catalyzed Hydroarylations of Alkynes under Ball-Milling Conditions
DOI:
10.1021/acs.orglett.7b02973
Non-Metal-Catalyzed Heterodehydrocoupling of Phosphines and Hydrosilanes: Mechanistic Studies of B(C6F5)3-Mediated Formation of P–Si Bonds
DOI:
10.1021/jacs.7b09175
Electronic Effects on Room-Temperature, Gas-Phase C–H Bond Activations by Cluster Oxides and Metal Carbides: The Methane Challenge
DOI:
10.1021/jacs.7b10139
Experimental and Theoretical Studies on Iron-Promoted Oxidative Annulation of Arylglyoxal with Alkyne: Unusual Addition and Migration on the Aryl Ring
DOI:
10.1021/jacs.7b05981
Selective ortho C–H Activation of Pyridines Directed by Lewis Acidic Boron of PBP Pincer Iridium Complexes
10.1021/jacs.7b10570
Diastereodivergent Asymmetric Carboamination/Annulation of Cyclopropenes with Aminoalkenes by Chiral Lanthanum Catalysts
10.1021/jacs.7b10786
Sunday, November 5, 2017
Mechanism of Nakamura’s Bisphosphine-Iron-Catalyzed Asymmetric C(sp2)–C(sp3) Cross-Coupling Reaction: The Role of Spin in Controlling Arylation Pathways
Cation Radical Accelerated Nucleophilic Aromatic Substitution via Organic Photoredox Catalysis
Cooperative Al–H Bond Activation in DIBAL-H: Catalytic Generation of an Alumenium-Ion-Like Lewis Acid for Hydrodefluorinative Friedel–Crafts Alkylation
Versatile Alkylation of (Hetero)Aryl Iodides with Ketones via β-C(sp3)–H Activation
Rhodium/Copper Cocatalyzed Highly trans-Selective 1,2-Diheteroarylation of Alkynes with Azoles via C–H Addition/Oxidative Cross-Coupling: A Combined Experimental and Theoretical Study
Enantioselective Decarboxylative Cyanation Employing Cooperative Photoredox Catalysis and Copper Catalysis
Chemoselective Intermolecular Cross-Enolate-Type Coupling of Amides
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Coupling N–H Deprotonation, C–H Activation, and Oxidation: Metal-Free C(sp3)–H Aminations with Unprotected Anilinesications)
Tuesday, October 31, 2017
Enantioselective Decarboxylative Cyanation Employing Cooperative Photoredox Catalysis and Copper Catalysis
Tridentate Directing Groups Stabilize 6-Membered Palladacycles in Catalytic Alkene Hydrofunctionalization
Monday, October 23, 2017
Ligand-Enabled γ-C(sp3)–H Cross-Coupling of Nosyl-Protected Amines with Aryl- and Alkylboron Reagents
Use of Electrochemistry in the Synthesis of Heterocyclic Structures
Three-Component Catalytic Carboxygenation of Activated Alkenes Enabled by Bimetallic Rh(III)/Cu(II) Catalysis
Rhodium-Catalyzed Direct Ortho C–H Arylation Using Ketone as Directing Group with Boron Reagent
Hydroxoiridium-Catalyzed Hydroarylation of Alkynes and Bicycloalkenes with N-Sulfonylbenzamides
Cobalt-Catalyzed Oxidative Cyclization of Benzamides with Maleimides: Synthesis of Isoindolone Spirosuccinimides
Iridium/Bipyridine-Catalyzed ortho-Selective C–H Borylation of Phenol and Aniline Derivatives
Rhodium-Catalyzed [4 + 3] Annulations of Sulfoximines with α,β-Unsaturated Ketones Leading to 1,2-Benzothiazepine 1-Oxides
Transition-Metal-Free C–CN/C–H Cross-Coupling: Effect of Cyano Group
Total Synthesis and Anti-inflammatory Evaluation of Penchinone A and Its Structural Analogues
Palladium-Catalyzed Direct C(sp2)–H ortho-Arylation of Anilides Using 2-Aminophenylpyrazole as the Directing Group
Sunday, October 22, 2017
A Mild Hydroaminoalkylation of Conjugated Dienes Using a Unified Cobalt and Photoredox Catalytic System
Factors Controlling the Reactivity and Chemoselectivity of Resonance Destabilized Amides in Ni-Catalyzed Decarbonylative and Nondecarbonylative Suzuki-Miyaura Coupling
Through-Space Activation Can Override Substituent Effects in Electrophilic Aromatic Substitution
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