| Literature DB >> 30485562 |
Mathieu Lesieur1, Claudio Battilocchio2,3, Ricardo Labes2, Jérôme Jacq1, Christophe Genicot1, Steven V Ley2, Patrick Pasau1.
Abstract
A fast, scalable, and safer Csp 3 -H oxidation of activated and un-activated aliphatic chains can be enabled by methyl(trifluoromethyl)dioxirane (TFDO). The continuous flow platform allows the in situ generation of TFDO gas and its rapid reactivity toward tertiary and benzylic Csp3 -H bonds. The process exhibits a broad scope and good functional group compatibility (28 examples, 8-99 %). The scalability of this methodology is demonstrated on 2.5 g scale oxidation of adamantane.Entities:
Keywords: Oxone; TFDO; dioxirane; flow; hydroxylation; oxidation
Year: 2018 PMID: 30485562 DOI: 10.1002/chem.201805657
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236