A general method for the efficient difluoromethylation of alcohols using commercially
available TMSCF2Br (TMS= trimethylsilyl) as a unique and practical difluorocarbene source …

Fluorinated organic compounds are becoming increasingly important in pharmaceuticals,
agrochemicals and materials science. The introduction of trifluoromethoxy groups into new …

Trifluoromethoxy‐substituted stereogenic centers can be constructed with high
enantioselectivity by a nickel‐catalyzed Suzuki–Miyaura coupling of readily available α …

Upon activation under superacid conditions, functionalized tailor‐made N‐SCF3
sulfenamides served as reagents for the trifluoromethylthiolation of aromatic amines. This …

Development of an efficient process that employs commercially available and cost effective
reagents for the synthesis of perfluoroalkoxylated aromatic compounds (Ar–ORF) remains a …

The preparation of F 3 CO-and F 2 HCO-analogues of Imidacloprid and Thiacloprid and the
evaluation of their biological activity have been performed. For this purpose, a first synthetic …

Synthesis and physical chemical properties of 2-amino-4-(trifluoromethoxy)butanoic acid –
a CF 3 O-containing analogue of natural lipophilic amino aci ... - Organic & Biomolecular …

(Hetero) aryloxytetrafluoroethylation of heteroaromatics and alkenes has been achieved by
visible-light photocatalysis utilizing readily synthesized oxyfluoroalkyl reagents. The mild …

This PhD thesis allowed the conception of new molecules for the development of novel
phytosanitary ingredients. First, the synthesis of alpha, alpha-difluoro-betahydroxy ketones …