World's Best Scientists 2026 revealed!
Edward M. Kosower

Edward M. Kosower

D-Index & Metrics

Chemistry

D-Index
67
Citations
17761
World Ranking
6837
National Ranking
47

Research.com Recognitions

  • 1989 - Fellow of the American Association for the Advancement of Science (AAAS)
  • 1977 - Fellow of John Simon Guggenheim Memorial Foundation
  • 1960 - Fellow of Alfred P. Sloan Foundation

Overview

Edward M. Kosower is affiliated with Tel Aviv University in Israel. Their academic career includes distinctions such as being named a Fellow of the American Association for the Advancement of Science (AAAS) in 1989. Earlier in their career, they were recognized as a Fellow of the John Simon Guggenheim Memorial Foundation in 1977 and as a Fellow of the Alfred P. Sloan Foundation in 1960.

Their research contributions span various scientific domains, although detailed information on specific fields of study, subfields, and main topics of work is not provided in the available data.

No recent papers, frequent co-authors, publication venues, or book publications have been listed, which limits the scope for describing their publication record or research collaborations.

The recognitions accumulated throughout their career reflect engagement with scientific communities and institutions known for fostering research development.

Best Publications

  • The Glutathione Status of Cells

    Nechama S. Kosower;Edward M. Kosower

  • The Effect of Solvent on Spectra. I. A New Empirical Measure of Solvent Polarity: Z-Values

    Edward M. Kosower

  • Diamide, a new reagent for the intracellular oxidation of glutathione to the disulfide.

    Nechama S. Kosower;Edward M. Kosower;Bilha Wertheim;Walter S. Correa

  • Stable Free Radicals. II. The Reduction of 1-Methyl-4-cyanopyridinium Ion to Methylviologen Cation Radical

    Edward M. Kosower;John L. Cotter

  • EXCITED STATE ELECTRON AND PROTON TRANSFERS

    Edward M. Kosower;Dan Huppert

  • Diamide: an oxidant probe for thiols.

    Nechama S. Kosower;Edward M. Kosower

  • An introduction to physical organic chemistry

    Edward M. Kosower

  • Bimane fluorescent labels: labeling of normal human red cells under physiological conditions.

    Nechama S. Kosower;Edward M. Kosower;Gerald L. Newton;Helen M. Ranney

  • Intramolecular donor-acceptor systems. 9. Photophysics of (phenylamino)naphthalenesulfonates: a paradigm for excited-state intramolecular charge transfer

    Edward M. Kosower

  • Analysis of biological thiols: Quantitative determination of thiols at the picomole level based upon derivatization with monobromobimanes and separation by cation-exchange chromatography

    Robert C. Fahey;Robert C. Fahey;Gerald L. Newton;Gerald L. Newton;Randel Dorian;Randel Dorian;Edward M. Kosower;Edward M. Kosower

  • Lest I Forget Thee, Glutathione …

    E M Kosower;E M Kosower;N S Kosower;N S Kosower

  • Intramolecular donor-acceptor systems. Radiative and nonradiative processes for the excited states of 2-N-arylamino-6-naphthalenesulfonates

    Edward M. Kosower;Hanna Dodiuk;Kazutake Tanizawa;Michael Ottolenghi

  • Plasmon-resonance-enhanced absorption and circular dichroism.

    Itai Lieberman;Gabriel Shemer;Tcipi Fried;Edward M. Kosower

  • The Effect of Solvent on Spectra. II. Correlation of Spectral Absorption Data with Z-Values

    Edward M. Kosower

  • Thiol labeling with bromobimanes

    Nechama S. Kosower;Edward M. Kosower

  • Glutathione. 8. The effects of glutathione disulfide on initiation of protein synthesis.

    Nechama S. Kosower;Grace A. Vanderhoff;Edward M. Kosower;Edward M. Kosower

  • Glutathione VII. Differentiation among substrates by the thiol-oxidizing agent, diamide

    Edward M. Kosower;Walter Correa;Bruce J. Kinon;Nechama S. Kosower

  • Solvent motion controls the rate of intramolecular electron transfer in solution

    Edward M. Kosower;Dan Huppert

  • Bromobimane probes for thiols.

    Edward M. Kosower;Nechama S. Kosower

  • The Effect of Solvent on Spectra. III. The Use of Z-Values in Connection with Kinetic Data

    Edward M. Kosower

  • Monosubstituted diazenes (diimides). Surprising intermediates

    Edward M. Kosower

Frequent Co-Authors

Nechama S. Kosower
Nechama S. Kosower Tel Aviv University
Dan Huppert
Dan Huppert Tel Aviv University
Israel Goldberg
Israel Goldberg Tel Aviv University
Gil Markovich
Gil Markovich Tel Aviv University
Abraham Katzir
Abraham Katzir Tel Aviv University
Peter L. Carlen
Peter L. Carlen University Health Network
Tim Hunt
Tim Hunt University of Cambridge
Gerald L. Newton
Gerald L. Newton University of California, San Diego
Simon L. Croft
Simon L. Croft London School of Hygiene & Tropical Medicine
Alan H. Fairlamb
Alan H. Fairlamb University of Dundee

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