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Trevor Hamlin

Chemiker

Name	Trevor Hamlin
Zeit	2012- (Wirkungsdaten)
Ort	Niederlande USA
Geschlecht	männlich
Akademischer Grad bzw. Titel	Dr.
Beruf	Chemiker (charakteristischer Beruf)
Variante	Trevor A. Hamlin T. A. Hamlin
Beziehung	Vrije Universiteit Amsterdam University of Connecticut Theoretische Chemie (Thema) Computational chemistry (Thema) Organische Chemie (Thema)
Quelle	Homepage: https://research.vu.nl/en/persons/trevor-a-hamlin (Stand: 20.10.2022) Homepage: https://www.theochem.nl/trevor-a-hamlin (Stand: 20.10.2022)
Datensatztyp	Person
GND-Nummer	1261101405
Datensatz-ID	1261101405
Beteiligt an alle anzeigen Radical Addition Reactions: Hierarchical Ab Initio Benchmark and DFT Performance Study C1‐4 Alkylation of Aryl Bromides with Light Alkanes enabled by Metallaphotocatalysis in Flow C1‐4 Alkylation of Aryl Bromides with Light Alkanes enabled by Metallaphotocatalysis in Flow Rational Design of Metallylenes for Hydrogenation Reactions Cobalt‐Catalyzed Enantio‐ and Regioselective C (sp 3)−H Alkenylation of Thioamides Cobalt‐Catalyzed Enantio‐ and Regioselective C (sp 3)−H Alkenylation of Thioamides S N 2 versus E2 Competition of Cyclic Ethers The Origin of Catalysis and Regioselectivity of Lewis Acid‐Catalyzed Diels‐Alder Reactions with Tropone ** Origin of Stereoselectivity in S E 2′ Reactions of Six‐membered Ring Oxocarbenium Ions Intermolecular Covalent Interactions: Nature and Directionality The Search for Enhanced σ‐Donor Ligands to Stabilize Boron‐Boron Multiple Bonds Palladium-catalyzed activation of H n A–AH n bonds (AH n = CH 3, NH 2, OH, F) Iron‐Catalysed Carbene Transfer to Isocyanides as a Platform for Heterocycle Synthesis How Bases Catalyze Diels‐Alder Reactions Rational Tuning of the Reactivity of Three‐Membered Heterocycle Ring Openings via S N 2 Reactions Methyl Substitution Destabilizes Alkyl Radicals Methyl Substitution Destabilizes Alkyl Radicals The 1,3‐Dipolar Cycloaddition: From Conception to Quantum Chemical Design How Ionization Catalyzes Diels–Alder Reactions How Ionization Catalyzes Diels–Alder Reactions C−X Bond Activation by Palladium: Steric Shielding versus Steric Attraction How Ionization Catalyzes Diels‐Alder Reactions C (sp n)−X (n=1–3) Bond Activation by Palladium B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order C (sp n)−X (n=1–3) Bond Activation by Iron Palladium‐Catalyzed Activation of Carbon–Halogen Bonds: Electrostatics‐Controlled Reactivity B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order Front Cover: B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order (ChemistryOpen 2/2022) The Chemical Bond: When Atom Size instead of Electronegativity Difference Determines Trend in Bond Strength The Chemical Bond: When Atom Size Instead of Electronegativity Difference Determines Trend in Bond Strength Radical Scavenging Potential of the Phenothiazine Scaffold: A Computational Analysis Switchable, Reagent‐Controlled Diastereodivergent Photocatalytic Carbocyclisation of Imine‐Derived α‐Amino Radicals Switchable, Reagent‐Controlled Diastereodivergent Photocatalytic Carbocyclisation of Imine‐Derived α‐Amino Radicals How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes Boron Tunneling in the “Weak” Bond‐Stretch Isomerization of N−B Lewis Adducts Origin of the α‐Effect in S N 2 Reactions Origin of the α‐Effect in S N 2 Reactions Origin of the α‐Effect in S N 2 Reactions Origin of the α‐Effect in S N 2 Reactions Palladium‐Catalyzed Cascade to Benzoxepins by Using Vinyl‐Substituted Donor–Acceptor Cyclopropanes Palladium‐Catalyzed Cascade to Benzoxepins by Using Vinyl‐Substituted Donor–Acceptor Cyclopropanes Lewis Acid‐Catalyzed Diels‐Alder Reactions: Reactivity Trends across the Periodic Table How Lewis Acids Catalyze Ene Reactions The Gauche Effect in XCH 2 CH 2 X Revisited How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes Front Cover: How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes (ChemPhysChem 22/2021) A Quantitative Molecular Orbital Perspective of the Chalcogen Bond Switch From Pauli‐Lowering to LUMO‐Lowering Catalysis in Brønsted Acid‐Catalyzed Aza‐Diels‐Alder Reactions A Quantitative Molecular Orbital Perspective of the Chalcogen Bond Bifunctional Hydrogen Bond Donor‐Catalyzed Diels–Alder Reactions: Origin of Stereoselectivity and Rate Enhancement Bifunctional Hydrogen Bond Donor‐Catalyzed Diels–Alder Reactions: Origin of Stereoselectivity and Rate Enhancement How Oriented External Electric Fields Modulate Reactivity How Oriented External Electric Fields Modulate Reactivity Not Carbon s–p Hybridization, but Coordination Number Determines C−H and C−C Bond Length Not Carbon s–p Hybridization, but Coordination Number Determines C−H and C−C Bond Length Regioselectivity of Epoxide Ring‐Openings via S N 2 Reactions Under Basic and Acidic Conditions Nature and Strength of Lewis Acid/Base Interaction in Boron and Nitrogen Trihalides Front Cover: Nature and Strength of Lewis Acid/Base Interaction in Boron and Nitrogen Trihalides (Chem. Asian J. 23/2020) How Alkali Cations Catalyze Aromatic Diels‐Alder Reactions A Unified Framework for Understanding Nucleophilicity and Protophilicity in the S N 2/E2 Competition

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Katalog der Deutschen Nationalbibliothek

Trevor Hamlin

Radical Addition Reactions: Hierarchical Ab Initio Benchmark and DFT Performance Study

C1‐4 Alkylation of Aryl Bromides with Light Alkanes enabled by Metallaphotocatalysis in Flow

C1‐4 Alkylation of Aryl Bromides with Light Alkanes enabled by Metallaphotocatalysis in Flow

Rational Design of Metallylenes for Hydrogenation Reactions

Cobalt‐Catalyzed Enantio‐ and Regioselective C (sp 3)−H Alkenylation of Thioamides

Cobalt‐Catalyzed Enantio‐ and Regioselective C (sp 3)−H Alkenylation of Thioamides

S N 2 versus E2 Competition of Cyclic Ethers

The Origin of Catalysis and Regioselectivity of Lewis Acid‐Catalyzed Diels‐Alder Reactions with Tropone **

Origin of Stereoselectivity in S E 2′ Reactions of Six‐membered Ring Oxocarbenium Ions

Intermolecular Covalent Interactions: Nature and Directionality

The Search for Enhanced σ‐Donor Ligands to Stabilize Boron‐Boron Multiple Bonds

Palladium-catalyzed activation of H n A–AH n bonds (AH n = CH 3, NH 2, OH, F)

Iron‐Catalysed Carbene Transfer to Isocyanides as a Platform for Heterocycle Synthesis

How Bases Catalyze Diels‐Alder Reactions

Rational Tuning of the Reactivity of Three‐Membered Heterocycle Ring Openings via S N 2 Reactions

Methyl Substitution Destabilizes Alkyl Radicals

Methyl Substitution Destabilizes Alkyl Radicals

The 1,3‐Dipolar Cycloaddition: From Conception to Quantum Chemical Design

How Ionization Catalyzes Diels–Alder Reactions

How Ionization Catalyzes Diels–Alder Reactions

C−X Bond Activation by Palladium: Steric Shielding versus Steric Attraction

How Ionization Catalyzes Diels‐Alder Reactions

C (sp n)−X (n=1–3) Bond Activation by Palladium

B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order

C (sp n)−X (n=1–3) Bond Activation by Iron

Palladium‐Catalyzed Activation of Carbon–Halogen Bonds: Electrostatics‐Controlled Reactivity

B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order

Front Cover: B‐DNA Structure and Stability: The Role of Nucleotide Composition and Order (ChemistryOpen 2/2022)

The Chemical Bond: When Atom Size instead of Electronegativity Difference Determines Trend in Bond Strength

The Chemical Bond: When Atom Size Instead of Electronegativity Difference Determines Trend in Bond Strength

Radical Scavenging Potential of the Phenothiazine Scaffold: A Computational Analysis

Switchable, Reagent‐Controlled Diastereodivergent Photocatalytic Carbocyclisation of Imine‐Derived α‐Amino Radicals

Switchable, Reagent‐Controlled Diastereodivergent Photocatalytic Carbocyclisation of Imine‐Derived α‐Amino Radicals

How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes

Boron Tunneling in the “Weak” Bond‐Stretch Isomerization of N−B Lewis Adducts

Origin of the α‐Effect in S N 2 Reactions

Origin of the α‐Effect in S N 2 Reactions

Origin of the α‐Effect in S N 2 Reactions

Origin of the α‐Effect in S N 2 Reactions

Palladium‐Catalyzed Cascade to Benzoxepins by Using Vinyl‐Substituted Donor–Acceptor Cyclopropanes

Palladium‐Catalyzed Cascade to Benzoxepins by Using Vinyl‐Substituted Donor–Acceptor Cyclopropanes

Lewis Acid‐Catalyzed Diels‐Alder Reactions: Reactivity Trends across the Periodic Table

How Lewis Acids Catalyze Ene Reactions

The Gauche Effect in XCH 2 CH 2 X Revisited

How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes

Front Cover: How Divalent Cations Interact with the Internal Channel Site of Guanine Quadruplexes (ChemPhysChem 22/2021)

A Quantitative Molecular Orbital Perspective of the Chalcogen Bond

Switch From Pauli‐Lowering to LUMO‐Lowering Catalysis in Brønsted Acid‐Catalyzed Aza‐Diels‐Alder Reactions

A Quantitative Molecular Orbital Perspective of the Chalcogen Bond

Bifunctional Hydrogen Bond Donor‐Catalyzed Diels–Alder Reactions: Origin of Stereoselectivity and Rate Enhancement

Bifunctional Hydrogen Bond Donor‐Catalyzed Diels–Alder Reactions: Origin of Stereoselectivity and Rate Enhancement

How Oriented External Electric Fields Modulate Reactivity

How Oriented External Electric Fields Modulate Reactivity

Not Carbon s–p Hybridization, but Coordination Number Determines C−H and C−C Bond Length

Not Carbon s–p Hybridization, but Coordination Number Determines C−H and C−C Bond Length

Regioselectivity of Epoxide Ring‐Openings via S N 2 Reactions Under Basic and Acidic Conditions

Nature and Strength of Lewis Acid/Base Interaction in Boron and Nitrogen Trihalides

Front Cover: Nature and Strength of Lewis Acid/Base Interaction in Boron and Nitrogen Trihalides (Chem. Asian J. 23/2020)

How Alkali Cations Catalyze Aromatic Diels‐Alder Reactions

A Unified Framework for Understanding Nucleophilicity and Protophilicity in the S N 2/E2 Competition