Ontology highlight
ABSTRACT:
SUBMITTER: Laudadio G
PROVIDER: S-EPMC6676414 | biostudies-literature | 2019 Jul
REPOSITORIES: biostudies-literature
Laudadio Gabriele G Bartolomeu Aloisio de A AA Verwijlen Lucas M H M LMHM Cao Yiran Y de Oliveira Kleber T KT Noël Timothy T
Journal of the American Chemical Society 20190717 30
Sulfonyl fluorides are valuable synthetic motifs for a variety of applications, among which sulfur(VI) fluoride exchange-based "click chemistry" is currently the most prominent. Consequently, the development of novel and efficient synthetic methods to access these functional groups is of great interest. Herein, we report a mild and environmentally benign electrochemical approach to prepare sulfonyl fluorides using thiols or disulfides, as widely available starting materials, in combination with ...[more]