Cover Feature: Stereospecific Radical Bromination of β‐Aryl Alcohols with Thiourea Additives Through A Serendipitous Discovery of A 1,2‐Aryl Migration (Chem. Eur. J. 19/2025)
Year: 2025
Type: article
Abstract: 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).
Source: Chemistry - A European Journal
Authors: Habib Assy, Uttam K. Mishra, Tom Rösler, Raman Khurana, N. Gabriel Lemcoff, Ofer Reany
Institutions: Ben-Gurion University of the Negev, Open University of Israel
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: bronze
OpenAlex ID: W4409176331