跳转至内容
Merck
CN

Copper-mediated trifluoromethylthiolation of α-diazoesters.

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

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.

材料
货号
品牌
产品描述

Sigma-Aldrich
N,N-二甲基乙酰胺, suitable for HPLC, ≥99.9%
Sigma-Aldrich
N,N-二甲基乙酰胺, puriss. p.a., ≥99.5% (GC)
Sigma-Aldrich
N,N-二甲基乙酰胺, ReagentPlus®, 99%
Sigma-Aldrich
N,N-二甲基乙酰胺, ReagentPlus®, ≥99%
Sigma-Aldrich
N,N-二甲基乙酰胺, suitable for peptide synthesis, ≥99.8% (GC)
Sigma-Aldrich
N,N-二甲基乙酰胺, spectrophotometric grade, ≥99%
Sigma-Aldrich
N,N-二甲基乙酰胺, anhydrous, 99.8%
USP
N,N-二甲基乙酰胺 溶液, United States Pharmacopeia (USP) Reference Standard
Supelco
N,N-二甲基乙酰胺, analytical standard