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Distortion/Interaction Analysis Reveals the Origins of Selectivities in Iridium-Catalyzed C–H Borylation of Substituted Arenes and 5-Membered Heterocycles
1 of 45 checkable references need attention · checked 2026-07-23
At the dated check, the references listed below either did not resolve in Crossref or DataCite, or carried a retraction notice. Each one is shown with the registry record that put it there.
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References needing attention
does not resolve to a known work10.1021/ja412563e.
The 44 checked references that resolve
resolves10.1038/nature06485
Catalytic C–H functionalization by metal carbenoid and nitrenoid insertion
resolves10.1351/pac200678071369
Iridium-catalyzed borylation of arenes and heteroarenes via C-H activation
resolves10.1021/ar200206a
Borylation and Silylation of C–H Bonds: A Platform for Diverse C–H Bond Functionalizations
resolves10.1021/ja053433g
Mechanism of the Mild Functionalization of Arenes by Diboron Reagents Catalyzed by Iridium Complexes. Intermediacy and Chemistry of Bipyridine-Ligated Iridium Trisboryl Complexes
resolves10.1021/ja0302937
Iridium-Catalyzed Borylation of Benzene with Diboron. Theoretical Elucidation of Catalytic Cycle Including Unusual Iridium(V) Intermediate
resolves10.1021/ja0173019
Mild Iridium-Catalyzed Borylation of Arenes. High Turnover Numbers, Room Temperature Reactions, and Isolation of a Potential Intermediate
resolves10.1002/1521-3773(20020816)41:16<3056::AID-ANIE3056>3.0.CO;2-#
A Stoichiometric Aromatic CH Borylation Catalyzed by Iridium(
<scp>I</scp>
)/2,2′‐Bipyridine Complexes at Room Temperature
resolves10.1039/b311103b
Room temperature borylation of arenes and heteroarenes using stoichiometric amounts of pinacolborane catalyzed by iridium complexes in an inert solventElectronic supplementary information (ESI) available: experimental procedures and spectral analyses of products. See http://www.rsc.org/suppdata/cc/b3/b311103b/
resolves10.1002/adsc.200303058
Iridium‐Catalyzed Direct Borylation of Five‐Membered Heteroarenes by Bis(pinacolato)diboron: Regioselective, Stoichiometric, and Room Temperature Reactions
resolves10.1016/S0040-4039(02)01135-8
Iridium-catalyzed C–H coupling reaction of heteroaromatic compounds with bis(pinacolato)diboron: regioselective synthesis of heteroarylboronates
resolves10.1039/c0cc02041a
Electronic effects in iridium C–H borylations: insights from unencumbered substrates and variation of boryl ligand substituents
resolves10.1039/c0dt00296h
Importance of palladium–carbon bond energies in direct arylation of polyfluorinated benzenes
resolves10.1021/ol301521n
Transition-State Metal Aryl Bond Stability Determines Regioselectivity in Palladium Acetate Mediated C–H Bond Activation of Heteroarenes
resolves10.1021/ja0734086
Distortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition Reactivity
resolves10.1021/ja075785o
Origin of Regioselectivity in Palladium-Catalyzed Cross-Coupling Reactions of Polyhalogenated Heterocycles
resolves10.1021/ja800009z
Theory of 1,3-Dipolar Cycloadditions: Distortion/Interaction and Frontier Molecular Orbital Models
resolves10.1021/ja809142x
Transition State Distortion Energies Correlate with Activation Energies of 1,4-Dihydrogenations and Diels−Alder Cycloadditions of Aromatic Molecules
resolves10.1021/ja9003624
Reactivity and Regioselectivity in 1,3-Dipolar Cycloadditions of Azides to Strained Alkynes and Alkenes: A Computational Study
resolves10.1021/jo102572x
Aromaticity and Activation Strain Analysis of [3 + 2] Cycloaddition Reactions between Group 14 Heteroallenes and Triple Bonds
resolves10.1021/jo202342q
Analysis of the Palladium-Catalyzed (Aromatic)C–H Bond Metalation–Deprotonation Mechanism Spanning the Entire Spectrum of Arenes
resolves10.1021/ja802533u
Analysis of the Concerted Metalation-Deprotonation Mechanism in Palladium-Catalyzed Direct Arylation Across a Broad Range of Aromatic Substrates
resolves10.1021/ja408073m
Dichotomous Hydrogen Atom Transfer vs Proton-Coupled Electron Transfer During Activation of X–H Bonds (X = C, N, O) by Nonheme Iron–Oxo Complexes of Variable Basicity
resolves10.1002/cphc.200700092
Transition‐State Energy and Position along the Reaction Coordinate in an Extended Activation Strain Model
resolves10.1039/b815665d
Relevance of cis- and trans-dichloride Ru intermediates in Grubbs-II olefin metathesis catalysis (H2IMesCl2RuCHR)
resolves10.1021/ja2082119
Asymmetric Rh(I)-Catalyzed Intramolecular [3 + 2] Cycloaddition of 1-Yne-vinylcyclopropanes for Bicyclo[3.3.0] Compounds with a Chiral Quaternary Carbon Stereocenter and Density Functional Theory Study of the Origins of Enantioselectivity
resolves10.1021/cs2005899
Cp* Iridium Precatalysts for Selective C–H Oxidation via Direct Oxygen Insertion: A Joint Experimental/Computational Study
resolves10.1002/chem.201101587
Mechanistic Origin of Ligand‐Controlled Regioselectivity in Pd‐Catalyzed CH Activation/Arylation of Thiophenes
resolves10.1021/ja210792e
Gold-Catalyzed Intermolecular Reactions of Propiolic Acids with Alkenes: [4 + 2] Annulation and Enyne Cross Metathesis
resolves10.1021/ja2108728
<i>Z</i>-Selectivity in Olefin Metathesis with Chelated Ru Catalysts: Computational Studies of Mechanism and Selectivity
resolves10.1021/ja304643e
Understanding Reactivity and Stereoselectivity in Palladium-Catalyzed Diastereoselective sp<sup>3</sup> C–H Bond Activation: Intermediate Characterization and Computational Studies
resolves10.1021/ja301108m
Decomposition Pathways of <i>Z</i>-Selective Ruthenium Metathesis Catalysts
resolves10.1016/S0022-328X(01)01079-8
Electronic structure and spectra of ruthenium diimine complexes by density functional theory and INDO/S. Comparison of the two methods
resolves10.1039/b913949d
Pronounced effects of substituents on the iridium-catalyzed borylation of aryl C–H bonds
resolves10.1021/om970705i
A Theoretical Study of the C−H Activation of Methane Derivatives. Significant Effects of Electron-Withdrawing Substituents
resolves10.1021/om990461x
Theoretical Study on σ-Bond Activation of (HO)<sub>2</sub>B−XH<sub>3</sub> by M(PH<sub>3</sub>)<sub>2</sub> (X = C, Si, Ge, or Sn; M = Pd or Pt). Noteworthy Contribution of the Boryl p<sub>π</sub> Orbital to M−Boryl Bonding and Activation of the B−X σ-Bond
resolves10.1021/ja0428309
Sterically Directed Functionalization of Aromatic C−H Bonds: Selective Borylation Ortho to Cyano Groups in Arenes and Heterocycles
The 6 references without a DOI — listed, not checked
no DOI — not checkedOrganic Syntheses via Boranes
no DOI — not checkedBorane Reagents
no DOI — not checkedTajuddin, H.; Harrisson, P.; Bitterlich, B.; Collings, J. C.; Sim, N.; Batsanov, A. S.; Cheung, M. S.; Kawamorita, S.; Maxwell, A. C.; Shukla, L.; Morris, J.; Lin, Z.; Marder, T. B.; Steel, P. G.Chem. Sci. 2012.
no DOI — not checkedGaussian 09
no DOI — not checkedGorelsky, S. I.AOMix: Program for Molecular Orbital Analysis, version 6.8,http://www.sg-chem.net,Ottawa, ON. 2013.
no DOI — not checkedOrganotransition Metal Chemistry: From Bonding to Catalysis
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