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Hyperconjugative, Secondary Orbital, Electrostatic, and Steric Effects on the Reactivities and Endo and Exo Stereoselectivities of Cyclopropene Diels–Alder Reactions

Journal of the American Chemical Society, 2016-12, Vol.138 (51), p.16731-16736

2016

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Role of Orbital Interactions and Activation Strain (Distortion Energies) on Reactivities in the Normal and Inverse Electron-Demand Cycloadditions of Strained and Unstrained Cycloalkenes

Journal of organic chemistry, 2017-08, Vol.82 (16), p.8668-8675

2017

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Secondary Orbital Interactions Enhance the Reactivity of Alkynes in Diels–Alder Cycloadditions

Journal of the American Chemical Society, 2019-02, Vol.141 (6), p.2224-2227

2019

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Differential Effects of Nitrogen Substitution in 5‐ and 6‐Membered Aromatic Motifs

Chemistry : a European journal, 2020-07, Vol.26 (41), p.8862-8866

2020

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Hyperconjugative Antiaromaticity Activates 4H‑Pyrazoles as Inverse-Electron-Demand Diels–Alder Dienes

Organic letters, 2019-10, Vol.21 (20), p.8492-8495

2019

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Readily Accessible Ambiphilic Cyclopentadienes for Bioorthogonal Labeling

Journal of the American Chemical Society, 2018-05, Vol.140 (20), p.6426-6431

2018

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Synthesis and Diels–Alder Reactivity of 4-Fluoro-4-Methyl-4H-Pyrazoles

International journal of molecular sciences, 2020-06, Vol.21 (11), p.3964

2020

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Origins of Selectivities in the Stork Diels–Alder Cycloaddition for the Synthesis of (±)-4-Methylenegermine

Organic letters, 2018-10, Vol.20 (19), p.6108-6111

2018

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Click Chemistry with Cyclopentadiene

Chemical reviews, 2021-06, Vol.121 (12), p.6777-6801

2021

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Coal characterization and coalbed methane potential of the Chico-Lomã Coalfield, Paraná Basin, Brazil – Results from exploration borehole CBM001-CL-RS

Energy exploration & exploitation, 2020-09, Vol.38 (5), p.1589-1630

2020

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Theoretical Analysis of Reactivity Patterns in Diels–Alder Reactions of Cyclopentadiene, Cyclohexadiene, and Cycloheptadiene with Symmetrical and Unsymmetrical Dienophiles

Journal of organic chemistry, 2015-04, Vol.80 (7), p.3530-3537

2015

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Hyperconjugative Aromaticity and Antiaromaticity Control the Reactivities and π‑Facial Stereoselectivities of 5‑Substituted Cyclopentadiene Diels–Alder Cycloadditions

Journal of organic chemistry, 2018-12, Vol.83 (23), p.14658-14666

2018

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Structural Distortion of Cycloalkynes Influences Cycloaddition Rates both by Strain and Interaction Energies

Chemistry : a European journal, 2019-05, Vol.25 (25), p.6342-6348

2019

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Schleyer hyperconjugative aromaticity and Diels-Alder reactivity of 5-substituted cyclopentadienes

Journal of computational chemistry, 2016-01, Vol.37 (1), p.117-123

2016

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Click Organocatalysis: Acceleration of Azide–Alkyne Cycloadditions with Mutually Orthogonal Click Reactions

Journal of organic chemistry, 2024-02, Vol.89 (4), p.2232-2237

2024

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Stable, Reactive, and Orthogonal Tetrazines: Dispersion Forces Promote the Cycloaddition with Isonitriles

Angewandte Chemie International Edition, 2019-07, Vol.58 (27), p.9043-9048

International ed. in English, 2019

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Computational study of an oxetane 4H-pyrazole as a Diels–Alder diene

Tetrahedron letters, 2023-10, Vol.130, p.154768, Article 154768

2023

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Geminal repulsion disrupts Diels–Alder reactions of geminally substituted cyclopentadienes and 4H-pyrazoles

Tetrahedron, 2021-07, Vol.91, p.132160, Article 132160

2021

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Depositional setting, petrology and chemistry of Permian coals from the Paraná Basin: 2. South Santa Catarina Coalfield, Brazil

International journal of coal geology, 2010-12, Vol.84 (3-4), p.213-236

2010

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Bioorthogonal 4H-pyrazole “click” reagents

Chemical communications (Cambridge, England), 2023-04, Vol.59 (30), p.4451-4454

2023

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Hyperconjugative Antiaromaticity Activates 4 H -Pyrazoles as Inverse-Electron-Demand Diels-Alder Dienes

Organic letters, 2019-10, Vol.21 (20), p.8492-8495

2019

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Taming the 1,5-sigmatropic shift across protonated spirocyclic 4 H -pyrazoles

Journal of physical organic chemistry, 2024-09, Vol.37 (9)

2024

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Taming the 1,5‐sigmatropic shift across protonated spirocyclic 4H‐pyrazoles

Journal of physical organic chemistry, 2024-09, Vol.37 (9), p.n/a

2024

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Bioorthogonal 4 H -pyrazole "click" reagents

Chemical communications (Cambridge, England), 2023-04, Vol.59 (30), p.4451-4454

2023

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Spirocyclization enhances the Diels-Alder reactivities of geminally substituted cyclopentadienes and 4 H -pyrazoles

Journal of physical organic chemistry, 2023-04, Vol.36 (4)

2023

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Hyperconjugative, Secondary Orbital, Electrostatic, and Steric Effects on the Reactivities and Endo and Exo Stereoselectivities of Cyclopropene Diels–Alder Reactions

Role of Orbital Interactions and Activation Strain (Distortion Energies) on Reactivities in the Normal and Inverse Electron-Demand Cycloadditions of Strained and Unstrained Cycloalkenes

Secondary Orbital Interactions Enhance the Reactivity of Alkynes in Diels–Alder Cycloadditions

Differential Effects of Nitrogen Substitution in 5‐ and 6‐Membered Aromatic Motifs

Hyperconjugative Antiaromaticity Activates 4H‑Pyrazoles as Inverse-Electron-Demand Diels–Alder Dienes

Readily Accessible Ambiphilic Cyclopentadienes for Bioorthogonal Labeling

Synthesis and Diels–Alder Reactivity of 4-Fluoro-4-Methyl-4H-Pyrazoles

Origins of Selectivities in the Stork Diels–Alder Cycloaddition for the Synthesis of (±)-4-Methylenegermine

Click Chemistry with Cyclopentadiene

Coal characterization and coalbed methane potential of the Chico-Lomã Coalfield, Paraná Basin, Brazil – Results from exploration borehole CBM001-CL-RS

Theoretical Analysis of Reactivity Patterns in Diels–Alder Reactions of Cyclopentadiene, Cyclohexadiene, and Cycloheptadiene with Symmetrical and Unsymmetrical Dienophiles

Hyperconjugative Aromaticity and Antiaromaticity Control the Reactivities and π‑Facial Stereoselectivities of 5‑Substituted Cyclopentadiene Diels–Alder Cycloadditions

Structural Distortion of Cycloalkynes Influences Cycloaddition Rates both by Strain and Interaction Energies

Schleyer hyperconjugative aromaticity and Diels-Alder reactivity of 5-substituted cyclopentadienes

Click Organocatalysis: Acceleration of Azide–Alkyne Cycloadditions with Mutually Orthogonal Click Reactions

Stable, Reactive, and Orthogonal Tetrazines: Dispersion Forces Promote the Cycloaddition with Isonitriles

Computational study of an oxetane 4H-pyrazole as a Diels–Alder diene

Geminal repulsion disrupts Diels–Alder reactions of geminally substituted cyclopentadienes and 4H-pyrazoles

Depositional setting, petrology and chemistry of Permian coals from the Paraná Basin: 2. South Santa Catarina Coalfield, Brazil

Bioorthogonal 4H-pyrazole “click” reagents

Hyperconjugative Antiaromaticity Activates 4 H -Pyrazoles as Inverse-Electron-Demand Diels-Alder Dienes

Taming the 1,5-sigmatropic shift across protonated spirocyclic 4 H -pyrazoles

Taming the 1,5‐sigmatropic shift across protonated spirocyclic 4H‐pyrazoles

Bioorthogonal 4 H -pyrazole "click" reagents

Spirocyclization enhances the Diels-Alder reactivities of geminally substituted cyclopentadienes and 4 H -pyrazoles

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