Christopher J. Evoniuk

Author

Florida State University ORCID

Also Known As

Christopher Evoniuk, Christopher J. Evoniuk, Evoniuk, Christopher J.

Publications

431

Citations

H-Index

Concepts

All Affiliations

Florida State University Tallahassee Orthopedic Clinic

About

Christopher J. Evoniuk is an author at Florida State University specializing in engineering, organic chemistry, and biomolecular engineering.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	4	4	222
2	Biomolecular Engineering	4	4	222
3	Chemistry	4	4	222
4	Natural Sciences	2	2	112
5	Chemical Engineering	1	1	13

Christopher J. Evoniuk

Publications

431

Citations

H-Index

Page 1

	Year	Citations
Alkenes as Alkyne Equivalents in Radical Cascades Terminated by Fragmentations: Overcoming Stereoelectronic Restrictions on Ring Expansions for the Preparation of Expanded Polyaromatics Rana K. Mohamed, Sayantan Mondal, Brian Gold, Journal of the American Chemical Society EngineeringOrganic ChemistryChemistryExpanded PolyaromaticsRadical Cascades Terminated	2015	99
Coupling N–H Deprotonation, C–H Activation, and Oxidation: Metal-Free C(sp<sup>3</sup>)–H Aminations with Unprotected Anilines Christopher J. Evoniuk, Gabriel dos Passos Gomes, Sean P. Hill, Journal of the American Chemical Society	2017	97
Coupling cyclizations with fragmentations for the preparation of heteroaromatics: quinolines from o-alkenyl arylisocyanides and boronic acids Christopher J. Evoniuk, Michelle Ly, Igor V. Alabugin Chemical Communications Reaction CascadesCross-coupling ReactionEngineeringHeterocyclicAlkene Metathesis	2015	61
Coupling Radical Homoallylic Expansions with C–C Fragmentations for the Synthesis of Heteroaromatics: Quinolines from Reactions of <i>o</i>-Alkenylarylisonitriles with Aryl, Alkyl, and Perfluoroalkyl Radicals Christopher J. Evoniuk, Gabriel dos Passos Gomes, Michelle Ly, The Journal of Organic Chemistry Reaction CascadesCross-coupling ReactionEngineeringSelective AdditionHeterocyclic	2017	49
Testing the limits of radical-anionic CH-amination: a 10-million-fold decrease in basicity opens a new path to hydroxyisoindolines<i>via</i>a mixed C–N/C–O-forming cascade Quintin Elliott, Gabriel dos Passos Gomes, Christopher J. Evoniuk, Chemical Science	2020	44
Double C–H amination by consecutive SET oxidations Christopher J. Evoniuk, Sean P. Hill, Kenneth Hanson, Chemical Communications	2016	39
Exploring anion-induced conformational flexibility and molecular switching in a series of heteroaryl-urea receptors Jesse V. Gavette, Christopher J. Evoniuk, Lev N. Zakharov, Chemical Science	2014	29
Changing the path of least resistance, or access to endo-dig products via a sequence of three exo-trig transition states: electronic effects in homoallyic ring expansion cascades of alkenyl isonitriles Gabriel dos Passos Gomes, Christopher J. Evoniuk, Michelle Ly, Organic & Biomolecular Chemistry EngineeringExpansion CascadesOrganic ChemistryLeast ResistanceComputational Chemistry	2017	13

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