Metal-Free HB(C6F5)2-Catalyzed Hydrogenation of Unfunctionalized Olefins and Mechanism Study of Borane-Mediated σ-Bond Metathesis

Functional-Group Tolerance in Frustrated Lewis Pairs: Hydrogenation of Nitroolefins and Acrylates

(2013) Lutz Greb et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Frustrated Lewis Pair Induced Boroauration of Terminal Alkynes

(2012) Hongyan Ye et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Metal-free Catalytic Olefin Hydrogenation: Low-Temperature H2 Activation by Frustrated Lewis Pairs

(2012) Lutz Greb et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Metal-Free Hydrogenation of Electron-Poor Allenes and Alkenes

(2012) Blanca Inés et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Metal-free hydrogenation catalysis of polycyclic aromatic hydrocarbons

(2012) Yasutomo Segawa et al.   CHEMICAL COMMUNICATIONS

Metal-Free Aromatic Hydrogenation: Aniline to Cyclohexyl-amine Derivatives

(2012) Tayseer Mahdi et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Facile Activation of H–H and Si–H Bonds by Boranes

(2012) Georgii I. Nikonov et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Mechanistic Studies on the Metal-Free Activation of Dihydrogen by Antiaromatic Pentarylboroles

(2012) Adrian Y. Houghton et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

High-Activity Iron Catalysts for the Hydrogenation of Hindered, Unfunctionalized Alkenes

(2012) Renyuan Pony Yu et al.   ACS Catalysis

Heterolytic Cleavage of Dihydrogen by “Frustrated Lewis Pairs” Comprising Bis(2,4,6-tris(trifluoromethyl)phenyl)borane and Amines: Stepwise versus Concerted Mechanism

(2011) Zhenpin Lu et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Reaction of Frustrated Lewis Pairs with Conjugated Ynones-Selective Hydrogenation of the Carbon-Carbon Triple Bond

(2011) Bao-Hua Xu et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

CO2 and Formate Complexes of Phosphine/Borane Frustrated Lewis Pairs

(2011) Ilona Peuser et al.   CHEMISTRY-A EUROPEAN JOURNAL

Metal-Free Catalytic Hydrogenation of Polar Substrates by Frustrated Lewis Pairs

(2011) Douglas W. Stephan et al.   INORGANIC CHEMISTRY

Expanding the Scope of Metal-Free Catalytic Hydrogenation through Frustrated Lewis Pair Design

(2010) Gábor Erős et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Enantioselective Hydrogenation with Chiral Frustrated Lewis Pairs

(2010) Dianjun Chen et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Metal-free reductions of N-heterocycles via Lewis acid catalyzed hydrogenation

(2010) Stephen J. Geier et al.   CHEMICAL COMMUNICATIONS

Reversible, metal-free hydrogenactivation by frustrated Lewis pairs

(2010) Chunfang Jiang et al.   DALTON TRANSACTIONS

Dihydrogen Activation by Antiaromatic Pentaarylboroles

(2010) Cheng Fan et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Frustrated Lewis Pairs: Metal-free Hydrogen Activation and More

(2009) Douglas W. Stephan et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Metal-free hydrogen activation and hydrogenation of imines by 1,8-bis(dipentafluorophenylboryl)naphthalene

(2009) Chunfang Jiang et al.   CHEMICAL COMMUNICATIONS

Metal-Free Catalytic Hydrogenation of Enamines, Imines, and Conjugated Phosphinoalkenylboranes

(2008) Patrick Spies et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Early Main-Group Metal Catalysts for the Hydrogenation of Alkenes with H2

(2008) Jan Spielmann et al.   ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

Lewis acid-catalyzed hydrogenation: B(C6F5)3-mediated reduction of imines and nitriles with H2

(2008) Preston A. Chase et al.   CHEMICAL COMMUNICATIONS

Heterolytic dihydrogen activation with the 1,8-bis(diphenylphosphino)naphthalene/B(C6F5)3 pair and its application for metal-free catalytic hydrogenation of silyl enol ethers

(2008) Huadong Wang et al.   CHEMICAL COMMUNICATIONS

Metal-free catalytic hydrogenation of imines with tris(perfluorophenyl)borane

(2008) Dianjun Chen et al.   CHEMICAL COMMUNICATIONS

Molecular Tweezers for Hydrogen: Synthesis, Characterization, and Reactivity

(2008) Victor Sumerin et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY