• 2248 Citations
  • 17 h-Index
20092019
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Fingerprint Dive into the research topics where Todd K. Hyster is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 7 Similar Profiles
Rhodium Chemical Compounds
Chemical activation Chemical Compounds
Benzamides Chemical Compounds
Enzymes Engineering & Materials Science
Alkenes Chemical Compounds
Amides Chemical Compounds
Regioselectivity Chemical Compounds
Catalysts Chemical Compounds

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Research Output 2009 2019

  • 2248 Citations
  • 17 h-Index
  • 19 Article
  • 3 Review article
  • 2 Comment/debate

Biocatalytic hydrogen atom transfer: an invigorating approach to free-radical reactions

Nakano, Y., Biegasiewicz, K. F. & Hyster, T. K., Apr 1 2019, In : Current Opinion in Chemical Biology. 49, p. 16-24 9 p.

Princeton University

Research output: Contribution to journalReview article

Free radical reactions
Free Radicals
Hydrogen
Atoms
Biocatalysis

Photoenzymatic Catalysis Enables Radical-Mediated Ketone Reduction in Ene-Reductases

Sandoval, B. A., Kurtoic, S. I., Chung, M. M., Biegasiewicz, K. F. & Hyster, T. K., Jun 24 2019, In : Angewandte Chemie - International Edition. 58, 26, p. 8714-8718 5 p.

Princeton University

Research output: Contribution to journalArticle

Ketones
Catalysis
Oxidoreductases
Enzymes
Alkenes
10 Citations (Scopus)

Catalytic promiscuity enabled by photoredox catalysis in nicotinamide-dependent oxidoreductases

Biegasiewicz, K. F., Cooper, S. J., Emmanuel, M. A., Miller, D. C. & Hyster, T. K., Jul 1 2018, In : Nature chemistry. 10, 7, p. 770-775 6 p.

Princeton University

Research output: Contribution to journalArticle

Niacinamide
Catalysis
Oxidoreductases
Enzymes
Photocatalysts
1 Citation (Scopus)
Isomers
Chemical activation
Ligands
Regioselectivity
Alkenes
21 Citations (Scopus)

Enantioselective Hydrogen Atom Transfer: Discovery of Catalytic Promiscuity in Flavin-Dependent 'Ene'-Reductases

Sandoval, B. A., Meichan, A. J. & Hyster, T. K., Aug 23 2017, In : Journal of the American Chemical Society. 139, 33, p. 11313-11316 4 p.

Princeton University

Research output: Contribution to journalArticle

Hydrogen
Oxidoreductases
Reducing Agents
Dehalogenation
Atoms