Journal Articles

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Catalytic Hydroarylation of Olefins with Phenols using B(C6F5)3, Organometallics, 2018, 37, 3654–3658

Substituent Effects on the Lewis Acidity of 4,6-Di-tertbutylcatechol Boronate Esters, Tetrahedron, 2019, 75, 31–35.

A Simple and Effective Method of Determining Lewis Acidity Using Fluorescence, Chem ,2019,5, 1567–1583.

Lewis Acidity of Organofluorophosphonium Salts: Hydrodefluorination by a Saturated Acceptor, Science,2013,341, 1374–1377.

Olefin Isomerization and Hydrosilylation Catalysis by Lewis Acidic Organofluorophosphonium Salts, J. Am. Chem. Soc.,2013,135, 18308–18310.

Reactivity of an Intramolecular Fluorophosphonium-Fluoroborate, Chem. Eur. J.,,2014,20, 11287–11290.

Olefin Transfer Hydrogenation via Electrophilic Phosphonium Catalysis of Heteroatom-Silane Dehydrocoupling, Proc. Nat. Acad. Sci.,2014,111, 10917–10921.

Electrophilic Phosphonium Cation Hydrosilylation Catalysis of Ketones, Imines and Nitriles, Selectivity and Mechanism, Chem. Eur. J.,2015,21, 6491–6500.

Synthesis and Lewis Acidity of Fluorophosphonium Cations, Dalton Trans.,2015,44, 12256–12264.

Electrophilic Fluorophosphonium Cations in FLP Hydrogen Activation and Catalytic Hydrogenation of Olefins, Angew. Chem. Int. Ed.,2015,54, 10178–10182.

Use of Trifluoromethyl Groups for Catalytic Benzylation and Alkylation with Subsequent Hydrodefluorination, Angew. Chem. Int. Ed.,2016,55, 1417–1421.

Non-Conventional Lewis acids and bases in Frustrated Lewis pair chemistry, Structure and Bonding ,2017,The Chemical Bond III: 100 Years Old and Getting Stronger, 1–29.