Peter R. Schreiner

Research interests

Publications

• Tunneling Control of Chemical Reactions: The Third Reactivity Paradigm

  Journal of the American Chemical Society · 2017 · 10.1021/jacs.7b06035

• Computational Chemistry: The Fate of Current Methods and Future Challenges

  Angewandte Chemie International Edition · 2017 · 10.1002/anie.201709943

• London’sche Dispersionswechselwirkungen in der Molekülchemie – eine Neubetrachtung sterischer Effekte

  Angewandte Chemie · 2015 · 10.1002/ange.201503476

• London Dispersion in Molecular Chemistry—Reconsidering Steric Effects

  Angewandte Chemie International Edition · 2015 · https://doi.org/10.1002/anie.201503476

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

  Chemical Reviews · 2013 · https://doi.org/10.1021/cr100264t

• Evolution of asymmetric organocatalysis: multi- and retrocatalysis

  Green Chemistry · 2012 · 10.1039/c2gc35160a

• Stable Alkanes Containing Very Long Carbon–Carbon Bonds

  Journal of the American Chemical Society · 2012 · 10.1021/ja302258q

• (Thio)urea Organocatalyst Equilibrium Acidities in DMSO

  Organic Letters · 2012 · 10.1021/ol300307c

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

  European Journal of Organic Chemistry · 2012 · 10.1002/ejoc.201200739

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

  Angewandte Chemie International Edition · 2011 · 10.1002/anie.201103615

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

  Angewandte Chemie International Edition · 2011 · 10.1002/anie.201006128

• Methylhydroxycarbene: Tunneling Control of a Chemical Reaction

  Science · 2011 · 10.1126/science.1203761

• Overcoming lability of extremely long alkane carbon–carbon bonds through dispersion forces

  Nature · 2011 · 10.1038/nature10367

• (Thio)urea organocatalysis—What can be learnt from anion recognition?

  Chemical Society Reviews · 2009 · https://doi.org/10.1039/b801793j

• Capture of hydroxymethylene and its fast disappearance through tunnelling

  Nature · 2008 · 10.1038/nature07010

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

  Angewandte Chemie International Edition · 2007 · 10.1002/anie.200701684

• How Accurate Are DFT Treatments of Organic Energies?

  Organic Letters · 2007 · 10.1021/ol070354w

• Many Density Functional Theory Approaches Fail To Give Reliable Large Hydrocarbon Isomer Energy Differences

  Organic Letters · 2006 · 10.1021/ol0610486

• Acid-free, organocatalytic acetalization

  Tetrahedron · 2005 · 10.1016/j.tet.2005.09.079

• Metal‐Free, Noncovalent Catalysis of Diels–Alder Reactions by Neutral Hydrogen Bond Donors in Organic Solvents and in Water

  Chemistry - A European Journal · 2003 · 10.1002/chem.200390042

• Metal-free organocatalysis through explicit hydrogen bonding interactions

  Chemical Society Reviews · 2003 · https://doi.org/10.1039/b107298f

• H-Bonding Additives Act Like Lewis Acid Catalysts

  Organic Letters · 2002 · https://doi.org/10.1021/ol017117s

• Selective Alkane Transformations via Radicals and Radical Cations: Insights into the Activation Step from Experiment and Theory

  Chemical Reviews · 2002 · 10.1021/cr000453m

• Consequences of Triplet Aromaticity in 4nπ-Electron Annulenes: Calculation of Magnetic Shieldings for Open-Shell Species

  Angewandte Chemie International Edition · 1998 · 10.1002/(sici)1521-3773(19980803)37:13/14<1945::aid-anie1945>3.0.co;2-e

• CH+5: The never-ending story or the final word?

  The Journal of Chemical Physics · 1993 · 10.1063/1.466147

Current projects

No projects listed.