Accéder au contenu
Merck

Copper-mediated trifluoromethylthiolation of α-diazoesters.

Organic letters (2014-03-26)
Mingyou Hu, Jian Rong, Wenjun Miao, Chuanfa Ni, Yongxin Han, Jinbo Hu
RÉSUMÉ

A novel Cu-mediated trifluoromethylthiolation of diazo compounds has been developed that provides a convenient synthetic route for the efficient α-trifluoromethylthiolation of simple esters under mild reaction conditions. The reaction is typically carried out at room temperature, and water could be used to promote the reaction.

MATÉRIAUX
Référence du produit
Marque
Description du produit

Sigma-Aldrich
N,N-diméthylacétamide, suitable for HPLC, ≥99.9%
Sigma-Aldrich
N,N-diméthylacétamide, ReagentPlus®, ≥99%
Sigma-Aldrich
N,N-diméthylacétamide, ReagentPlus®, 99%
Sigma-Aldrich
N,N-diméthylacétamide, anhydrous, 99.8%
Sigma-Aldrich
N,N-diméthylacétamide, suitable for peptide synthesis, ≥99.8% (GC)
Sigma-Aldrich
N,N-diméthylacétamide, spectrophotometric grade, ≥99%
Supelco
N,N-diméthylacétamide, analytical standard
USP
Residual Solvent Class 2 - N,N-Dimethylacetamide, United States Pharmacopeia (USP) Reference Standard