AI Article Synopsis

  • - A new method for nucleophilic trifluoromethylation of carbonyl compounds using gaseous fluoroform has been created, featuring a micro-flow process.
  • - This technique successfully transforms -sulfinylimines into trifluoromethyl amines with high diastereoselectivity.
  • - The application of this micro-flow synthesis is showcased through the formal synthesis of the drug Efavirenz.

Article Abstract

A micro-flow nucleophilic trifluoromethylation of carbonyl compounds using gaseous fluoroform was developed. This method also allows the first micro-flow transformation of -sulfinylimines into trifluoromethyl amines with excellent diastereoselectivity. To demonstrate the synthetic utility of this micro-flow synthesis, the formal micro-flow synthesis of Efavirenz is described.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442697PMC
http://dx.doi.org/10.1002/open.201800286DOI Listing

Publication Analysis

Top Keywords

micro-flow synthesis
8
gas/liquid-phase micro-flow
4
micro-flow trifluoromethylation
4
trifluoromethylation fluoroform
4
fluoroform trifluoromethylation
4
trifluoromethylation aldehydes
4
aldehydes ketones
4
ketones chalcones
4
chalcones -sulfinylimines
4
micro-flow
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!