Overriding Nitrogen-Centered Reactivity of Sulfinamidyl Radicals Enables Sulfoximine Synthesis.
- DOI
- 10.1021/jacs.6c10408
- Published
- 2026 Sep 23
- Container
- Journal of the American Chemical Society
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1021/jacs.6c10408,
title = {Overriding Nitrogen-Centered Reactivity of Sulfinamidyl Radicals Enables Sulfoximine Synthesis.},
author = {Glossbrenner MD and González-Granda S and Farmer LA and Noten EA and Kamal S and Balintfy CM and Nayal OS and Pratt DA and Stephenson CRJ},
year = {2026},
journal = {Journal of the American Chemical Society},
doi = {10.1021/jacs.6c10408},
url = {https://doi.org/10.1021/jacs.6c10408}
}RIS
TY - JOUR TI - Overriding Nitrogen-Centered Reactivity of Sulfinamidyl Radicals Enables Sulfoximine Synthesis. AU - Glossbrenner MD AU - González-Granda S AU - Farmer LA AU - Noten EA AU - Kamal S AU - Balintfy CM AU - Nayal OS AU - Pratt DA AU - Stephenson CRJ PY - 2026 JO - Journal of the American Chemical Society DO - 10.1021/jacs.6c10408 UR - https://doi.org/10.1021/jacs.6c10408 ER -
APA
MD, G., S, G., LA, F., EA, N., S, K., CM, B., OS, N., DA, P., & CRJ, S. (2026). Overriding Nitrogen-Centered Reactivity of Sulfinamidyl Radicals Enables Sulfoximine Synthesis.. Journal of the American Chemical Society. https://doi.org/10.1021/jacs.6c10408
Source records
- pubmed · retrieved 2026-11-10T11:18:43.500Z