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Tunneling Control of Chemical Reactions: The Third Reactivity Paradigm

Journal of the American Chemical Society, 2017-11, Vol.139 (43), p.15276-15283

Schreiner, Peter R

2017

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Computational Chemistry: The Fate of Current Methods and Future Challenges

Angewandte Chemie International Edition, 2018-04, Vol.57 (16), p.4170-4176

International ed. in English, 2018

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London Dispersion in Molecular Chemistry-Reconsidering Steric Effects

Angewandte Chemie (International ed.), 2015-10, Vol.54 (42), p.12274-12296

International ed. in English, 2015

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The Lipophilic Bullet Hits the Targets: Medicinal Chemistry of Adamantane Derivatives

Chemical reviews, 2013-05, Vol.113 (5), p.3516-3604

2013

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London Dispersion Interactions Rather than Steric Hindrance Determine the Enantioselectivity of the Corey–Bakshi–Shibata Reduction

Angewandte Chemie (International ed.), 2021-02, Vol.60 (9), p.4823-4832

International ed. in English, 2021

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Steric Crowding Can Stabilize a Labile Molecule: Solving the Hexaphenylethane Riddle

Angewandte Chemie (International ed.), 2011-12, Vol.50 (52), p.12639-12642

International ed. in English, 2011

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Triplet Phenylarsinidene and Its Oxidation to Dioxophenylarsine

Journal of the American Chemical Society, 2023-06, Vol.145 (23), p.12755-12759

2023

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Evolution of asymmetric organocatalysis: multi- and retrocatalysis

Green chemistry : an international journal and green chemistry resource : GC, 2012-01, Vol.14 (7), p.1821-1849

2012

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Diamonds are a Chemist's Best Friend: Diamondoid Chemistry Beyond Adamantane

Angewandte Chemie (International ed.), 2008-01, Vol.47 (6), p.1022-1036

2008

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Metal-free organocatalysis through explicit hydrogen bonding interactions

Chemical Society reviews, 2003-09, Vol.32 (5), p.289-296

Schreiner, Peter R

2003

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Organocatalytic Enantioselective Acyl Transfer onto Racemic as well as meso Alcohols, Amines, and Thiols

Angewandte Chemie (International ed.), 2011-06, Vol.50 (27), p.6012-6042

International ed. in English, 2011

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Determination of the Absolute Configurations of Chiral Alkanes – An Analysis of the Available Tools

European journal of organic chemistry, 2020-10, Vol.2020 (40), p.6328-6339

2020

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Relative Energy Computations with Approximate Density Functional Theory-A Caveat

Angewandte Chemie (International ed.), 2007-01, Vol.46 (23), p.4217-4219

Schreiner, Peter R.

2007

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Sizing the role of London dispersion in the dissociation of all- meta tert -butyl hexaphenylethane

Chemical science (Cambridge), 2017-01, Vol.8 (1), p.405-410

2017

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(Thio)urea Organocatalyst Equilibrium Acidities in DMSO

Organic letters, 2012-04, Vol.14 (7), p.1724-1727

2012

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Formation of a Tunneling Product in the Photorearrangement of o‐Nitrobenzaldehyde

Angewandte Chemie International Edition, 2017-08, Vol.56 (32), p.9445-9448

International ed. in English, 2017

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Computational Chemistry as a Conceptual Game Changer: Understanding the Role of London Dispersion in Hexaphenylethane Derivatives (Gomberg Systems)

Israel journal of chemistry, 2022-02, Vol.62 (1-2), p.n/a

2022

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London Dispersion Favors Sterically Hindered Diarylthiourea Conformers in Solution

Angewandte Chemie (International ed.), 2022-07, Vol.61 (29), p.e202204393-n/a

International ed. in English, 2022

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Site‐Selective Acylation of Pyranosides with Immobilized Oligopeptide Catalysts in Flow

Chemistry : a European journal, 2023-03, Vol.29 (18), p.e202203002-n/a

2023

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Fluoride-Assisted Activation of Calcium Carbide: A Simple Method for the Ethynylation of Aldehydes and Ketones

Organic letters, 2015-06, Vol.17 (11), p.2808-2811

2015

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Hydrogen-Bonding Thiourea Organocatalysts: The Privileged 3,5-Bis(trifluoromethyl)phenyl Group

European journal of organic chemistry, 2012-10, Vol.2012 (30), p.5919-5927

2012

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Methylhydroxycarbene: Tunneling Control of a Chemical Reaction

Science (American Association for the Advancement of Science), 2011-06, Vol.332 (6035), p.1300-1303

2011

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Catalytic enantiocontrol over a non-classical carbocation

Nature chemistry, 2020-12, Vol.12 (12), p.1174-1179

2020

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London Dispersion Enables the Shortest Intermolecular Hydrocarbon H···H Contact

Journal of the American Chemical Society, 2017-06, Vol.139 (22), p.7428-7431

2017

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Overcoming lability of extremely long alkane carbon―carbon bonds through dispersion forces

Nature (London), 2011-09, Vol.477 (7364), p.308-311

2011

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Tunneling Control of Chemical Reactions: The Third Reactivity Paradigm

Computational Chemistry: The Fate of Current Methods and Future Challenges

London Dispersion in Molecular Chemistry-Reconsidering Steric Effects

The Lipophilic Bullet Hits the Targets: Medicinal Chemistry of Adamantane Derivatives

London Dispersion Interactions Rather than Steric Hindrance Determine the Enantioselectivity of the Corey–Bakshi–Shibata Reduction

Steric Crowding Can Stabilize a Labile Molecule: Solving the Hexaphenylethane Riddle

Triplet Phenylarsinidene and Its Oxidation to Dioxophenylarsine

Evolution of asymmetric organocatalysis: multi- and retrocatalysis

Diamonds are a Chemist's Best Friend: Diamondoid Chemistry Beyond Adamantane

Metal-free organocatalysis through explicit hydrogen bonding interactions

Organocatalytic Enantioselective Acyl Transfer onto Racemic as well as meso Alcohols, Amines, and Thiols

Determination of the Absolute Configurations of Chiral Alkanes – An Analysis of the Available Tools

Relative Energy Computations with Approximate Density Functional Theory-A Caveat

Sizing the role of London dispersion in the dissociation of all- meta tert -butyl hexaphenylethane

(Thio)urea Organocatalyst Equilibrium Acidities in DMSO

Formation of a Tunneling Product in the Photorearrangement of o‐Nitrobenzaldehyde

Computational Chemistry as a Conceptual Game Changer: Understanding the Role of London Dispersion in Hexaphenylethane Derivatives (Gomberg Systems)

London Dispersion Favors Sterically Hindered Diarylthiourea Conformers in Solution

Site‐Selective Acylation of Pyranosides with Immobilized Oligopeptide Catalysts in Flow

Fluoride-Assisted Activation of Calcium Carbide: A Simple Method for the Ethynylation of Aldehydes and Ketones

Hydrogen-Bonding Thiourea Organocatalysts: The Privileged 3,5-Bis(trifluoromethyl)phenyl Group

Methylhydroxycarbene: Tunneling Control of a Chemical Reaction

Catalytic enantiocontrol over a non-classical carbocation

London Dispersion Enables the Shortest Intermolecular Hydrocarbon H···H Contact

Overcoming lability of extremely long alkane carbon―carbon bonds through dispersion forces

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