| Literature DB >> 27119573 |
Pauline Rullière1, Patrick Cyr1, André B Charette1.
Abstract
The first in-flow difluorocarbene generation and addition to alkenes and alkynes is reported. The application of continuous flow technology allowed for the controlled generation of difluorocarbene from TMSCF3 and a catalytic quantity of NaI. The in situ generated electrophilic carbene reacts smoothly with a broad range of alkenes and alkynes, allowing the synthesis of the corresponding difluorocyclopropanes and difluorocyclopropenes. The reaction is complete within a 10 min residence time at high reaction concentrations. With a production flow rate of 1 mmol/min, continuous flow chemistry enables scale up of this process in a green, atom-economic, and safe manner.Entities:
Year: 2016 PMID: 27119573 DOI: 10.1021/acs.orglett.6b00573
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005