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Organic Letters|May 7, 2005
Electronic nature of N-heterocyclic carbene ligands: effect on the Suzuki reactionNiloufar Hadei, Eric Assen B Kantchev, Christopher J O'Brien, et al.
Analytical Biochemistry|August 10, 2013
Quantitative affinity electrophoresis of RNA-small molecule interactions by cross-linking the ligand to acrylamideSherry N Boodram, Lucas C McCann, Michael G Organ, et al.
The Journal of Organic Chemistry|October 8, 2005
Room-temperature Negishi cross-coupling of unactivated alkyl bromides with alkyl organozinc reagents utilizing a Pd/N-heterocyclic carbene catalystNiloufar Hadei, Eric Assen B Kantchev, Christopher J O'Brien, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|December 4, 2014
Solvent choice and kinetic isotope effects (KIEs) dramatically alter regioselectivity in the directed ortho metalation (DoM) of 1,5-dichloro-2,4-dimethoxybenzeneJennifer L Farmer, Robert D J Froese, Edward Lee-Ruff, et al.
Angewandte Chemie (International Ed. in English)|February 20, 2009
Pd-PEPPSI-IPent: an active, sterically demanding cross-coupling catalyst and its application in the synthesis of tetra-ortho-substituted biarylsMichael G Organ, Selçuk Calimsiz, Mahmoud Sayah, et al.
Chemical Communications (Cambridge, England)|September 18, 2012
Sterically demanding imidazolinium salts through the activation and cyclization of formamidesMichael Tsimerman, Debasis Mallik, Tsukasa Matsuo, et al.
Journal of Flow Chemistry|November 26, 2011
Accessing Stereochemically Rich Sultams via Microwave-Assisted, Continuous Flow Organic Synthesis (MACOS) Scale-outMichael G Organ, Paul R Hanson, Alan Rolfe, et al.
Bioorganic & Medicinal Chemistry|November 19, 2010
Thermodynamic and NMR analysis of inhibitor binding to dihydrofolate reductaseIhor Batruch, Eliott Javasky, Eric D Brown, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|July 19, 2012
Highly stereo- and regioselective hydrostannylation of internal alkynes promoted by simple boric acid in airMartins S Oderinde, Howard N Hunter, Robert D J Froese, et al.
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