Kenneth Nicholas

Department of Chemistry and Biochemistry University of Oklahoma, Norman, OK, United States 
Organic Chemistry
"Kenneth Nicholas"
Mean distance: (not calculated yet)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Gopaladasu TV, Nicholas KM. (2016) Carbon Monoxide (CO)- and Hydrogen-Driven, Vanadium-Catalyzed Deoxydehydration of Glycols Acs Catalysis. 6: 1901-1904
Nicholas KM. (2015) A Forty Year Odyssey in Metallo-Organic Chemistry. The Journal of Organic Chemistry. 80: 6943-50
Tran AT, Liu P, Houk KN, et al. (2014) Regioselectivity in the Cu(I)-catalyzed [4 + 2]-cycloaddition of 2-nitrosopyridine with unsymmetrical dienes. The Journal of Organic Chemistry. 79: 5617-26
John A, Byun J, Nicholas KM. (2013) Copper-catalyzed C(sp2)-H amidation of unactivated arenes by N-tosyloxycarbamates. Chemical Communications (Cambridge, England). 49: 10965-7
Kannappan R, Nicholas KM. (2013) Selection of chiral zinc catalysts for the kinetic resolution of esters via dynamic templating. Acs Combinatorial Science. 15: 90-100
Liu P, Nicholas KM. (2013) Mechanism of sulfite-driven, MeReO3-catalyzed deoxydehydration of glycols Organometallics. 32: 1821-1831
Carberry J, Irvin JA, Glatzhofer DT, et al. (2013) High molecular weight copolymers of vinylferrocene and 3-phenyl[5] ferrocenophane-1,5-dimethylene with various N-substituted maleimides Reactive and Functional Polymers. 73: 730-736
Denning AL, Dang H, Liu Z, et al. (2013) Deoxydehydration of glycols catalyzed by carbon-supported perrhenate Chemcatchem. 5: 3567-3570
John A, Nicholas KM. (2012) Palladium catalyzed C-H functionalization of O-arylcarbamates: selective ortho-bromination using NBS. The Journal of Organic Chemistry. 77: 5600-5
Volkman J, Nicholas KM. (2012) A synthetic quest for tris(imidazolyl) carboxylates and their metal complexes: Active site models for quercetin 2,3-dioxygenases and other non-heme redox metalloenzymes Tetrahedron. 68: 3368-3376
See more...