Cover Feature: Stereospecific Radical Bromination of <i>β</i>‐Aryl Alcohols with Thiourea Additives Through A Serendipitous Discovery of A 1,2‐Aryl Migration (Chem. Eur. J. 19/2025)
The Cover Feature shows a unique radical mechanism that allows fully stereoretentive bromination of beta-aryl alcohols under very mild conditions by using N-bromo-succinimide (NBS) and substoichiometric thiourea. More information can be found in the Research Article by N. G. Lemcoff O. Reany and co-workers (DOI: 10.1002/chem.202403831).
Authors
- T. Rosler
- Uttam K. Mishra (ORCID: https://orcid.org/0000-0003-3670-7107)
- N. Gabriel Lemcoff (ORCID: https://orcid.org/0000-0003-1254-1149)
- Ofer Reany (ORCID: https://orcid.org/0000-0003-1048-1947)
- Raman Khurana (ORCID: https://orcid.org/0000-0002-0790-5377)
- Habib Assy (ORCID: https://orcid.org/0000-0001-8649-6534)
Institutions
- Ben-Gurion University of the Negev (IL)
- Open University of Israel (IL)
Publication Details
- Journal
- Chemistry - A European Journal
- Published
- 2025-04-01
- DOI
- https://doi.org/10.1002/chem.202581903
- Primary Topic
- Radical Photochemical Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00