Dustin Haddenham

发表

Enantioselective reduction of α-substituted ketones mediated by the boronate ester TarB-NO2

B. Singaram, Scott Eagon, Nicolas R. Ball‐Jones, 2010 .

Lithium aminoborohydrides 16. Synthesis and reactions of monomeric and dimeric aminoboranes.

B. Singaram, Dustin Haddenham, C. Goralski, 2008, The Journal of organic chemistry.

Lithium aminoborohydrides 17. Palladium catalyzed borylation of aryl iodides, bromides, and triflates with diisopropylaminoborane prepared from lithium diisopropylaminoborohydride

C. Vu, B. Singaram, Scott Eagon, 2011 .

Reaction of InCl3 with various reducing agents: InCl3-NaBH4-mediated reduction of aromatic and aliphatic nitriles to primary amines.

B. Singaram, Angel Resendez, Scott Eagon, 2012, The Journal of organic chemistry.

Reductions of aliphatic and aromatic nitriles to primary amines with diisopropylaminoborane.

B. Singaram, Scott Eagon, Dustin Haddenham, 2009, The Journal of organic chemistry.

Reaction of InCl3 with Various Reducing Agents: InCl3—NaBH4-Mediated Reduction of Aromatic and Aliphatic Nitriles to Primary Amines.

B. Singaram, Angel Resendez, Scott Eagon, 2012 .

Asymmetric reductions using the chiral boronic ester TarB–H: a practical and inexpensive procedure for synthesizing chiral alcohols

B. Singaram, Scott Eagon, Dustin Haddenham, 2007 .

Reductions of aliphatic and aromatic nitriles to primary amines with diisopropylaminoborane.

B. Singaram, Scott Eagon, Dustin Haddenham, 2009, The Journal of organic chemistry.

Mild and expedient asymmetric reductions of α,β-unsaturated alkenyl and alkynyl ketones by TarB-NO2 and mechanistic investigations of ketone reduction.

B. Singaram, Scott Eagon, Jaime Z. Saavedra, 2010, The Journal of organic chemistry.

Lithium Aminoborohydrides. Part 17. Palladium Catalyzed Borylation of Aryl Iodides, Bromides, and Triflates with Diisopropylaminoborane Prepared from Lithium Diisopropylaminoborohydride.

C. Vu, B. Singaram, Scott Eagon, 2011 .

Synthesis and SAR of a novel metabotropic glutamate receptor 4 (mGlu4) antagonist: unexpected 'molecular switch' from a closely related mGlu4 positive allosteric modulator.

C. Lindsley, C. Hopkins, C. Niswender, 2011, Bioorganic & medicinal chemistry letters.