Andrew J. Eberhart

Sulfoxide-Directed Metal-Free ortho-Propargylation of Aromatics and Heteroaromatics

D. Procter, A. Carrër, E. Álvarez, 2015, Chemistry.

Nucleophilic ortho-propargylation of aryl sulfoxides: an interrupted Pummerer/allenyl thio-Claisen rearrangement sequence.

D. Procter, Andrew J. Eberhart, 2013, Angewandte Chemie.

Nucleophilic ortho allylation of aryl and heteroaryl sulfoxides.

D. Procter, J. Imbriglio, Andrew J. Eberhart, 2011, Organic letters.

Nucleophilic ortho-Allylation of Pyrroles and Pyrazoles: An Accelerated Pummerer/Thio-Claisen Rearrangement Sequence

D. Procter, Andrew J. Eberhart, Claudio Cicoira, 2013, Organic letters.

Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials† †Electronic supplementary information (ESI) available: Full experimental details, NMR spectra, CCDC numbers for X-ray structures, and details of preliminary materials evaluation

Daniel J. Tate, M. Turner, D. Procter, 2015, Chemical science.

Highly Chemoselective Reduction of Amides (Primary, Secondary, Tertiary) to Alcohols using SmI2/Amine/H2O under Mild Conditions

M. Szostak, M. Spain, D. Procter, 2014, Journal of the American Chemical Society.

Metal-Free CH-CH-Type Cross-Coupling of Arenes and Alkynes Directed by a Multifunctional Sulfoxide Group.

D. Procter, Andrew J. Eberhart, Jose A. Fernández‐Salas, 2016, Journal of the American Chemical Society.

Mechanism of SmI2/amine/H2O-promoted chemoselective reductions of carboxylic acid derivatives (esters, acids, and amides) to alcohols.

M. Szostak, M. Spain, D. Procter, 2014, The Journal of organic chemistry.

Sulfoxide-directed metal-free cross-couplings in the expedient synthesis of benzothiophene-based components of materials† †Electronic supplementary information (ESI) available: Full experimental details, NMR spectra, CCDC numbers for X-ray structures, and details of preliminary materials evaluation

Daniel J. Tate, M. Turner, D. Procter, 2015, Chemical science.