Ugochinyere N. Oloyede

ORCID: 0000-0003-0958-3241
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About
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Research Areas
  • Radical Photochemical Reactions
  • Sulfur-Based Synthesis Techniques
  • Catalytic C–H Functionalization Methods
  • Cyclopropane Reaction Mechanisms
  • Magnesium in Health and Disease
  • Synthesis and Biological Evaluation
  • Advanced Photocatalysis Techniques
  • Fluorine in Organic Chemistry
  • Organometallic Complex Synthesis and Catalysis
  • Heavy metals in environment
  • Heavy Metal Exposure and Toxicity

United States Military Academy
2023

Lehigh University
2020-2023

Abstract Irradiation of Cp 2 TiCl with green light leads to electronically excited [Cp ]*. This complex constitutes an efficient photoredox catalyst for the reduction epoxides and 5‐ exo cyclizations suitably unsaturated epoxides. To best our knowledge, system is first example a molecular titanium catalyst.

10.1002/anie.202001508 article EN cc-by Angewandte Chemie International Edition 2020-03-26

Abstract Irradiation of Cp 2 TiCl with green light leads to electronically excited [Cp ]*. This complex constitutes an efficient photoredox catalyst for the reduction epoxides and 5‐ exo cyclizations suitably unsaturated epoxides. To best our knowledge, system is first example a molecular titanium catalyst.

10.1002/ange.202001508 article EN cc-by Angewandte Chemie 2020-03-26

A metal-free addition of unactivated alkyl bromides to quinoxalin-2(1H)-ones is described. This method enables the construction valuable 3,3-disubstituted dihydroquinoxalin-2(1H)-ones bearing quaternary carbon centers under mild, visible-light photoredox catalysis. High functional group tolerance observed in both quinoxalinone and bromide partners. The ability scale up this was demonstrated photo-flow conditions enable gram-scale synthesis.

10.1021/acs.joc.3c01054 article EN The Journal of Organic Chemistry 2023-08-09

The coordination of small molecules to low valent titanium complexes provides a powerful platform for the transformation challenging substrates either through PCET reactions or bond-weakening induced by π-back donation electrons from Ti.

10.1039/d3dt03454b article EN other-oa Dalton Transactions 2023-12-20
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