Ontology highlight
ABSTRACT:
SUBMITTER: Yu C
PROVIDER: S-EPMC6916641 | biostudies-literature | 2019 Dec
REPOSITORIES: biostudies-literature
Yu Congjun C Patureau Frederic W FW
Angewandte Chemie (International ed. in English) 20191031 51
A metal free and highly regioselective oxidative arylation reaction of fluorophenols is described. The relative position of the fluoride leaving group (i.e., ortho or para) controls the 1,2 or 1,4 nature of the arylated quinone product, lending versatility and generality to this oxidative, defluorinative, arylation concept. ...[more]