A Robust, Eco‐Friendly Access to Secondary Thioamides through the Addition of Organolithium Reagents to Isothiocyanates in Cyclopentyl Methyl Ether (CPME)
The nucleophilic addition of widely available and variously functionalized organolithiumreagents to isothiocyanates represents a straightforward, high‐yielding, one‐pot method to access secondary thioamides. The simple reaction conditions required and the broad scope (>50 cases examples) makes it a robust and reliable method to access both simple and complex thioamides, including enantiopure ones
Environmentally friendly ynamide-mediated thioamidation of monothiocarboxylic acids with amines or ammonium hydroxide for the syntheses of thioamides and primary thioamides is described. Simple and mild reaction conditions enable the reaction to tolerate a wide variety of functional groups such as hydroxyl group, ester, tertiary amine, ketone, and amide moieties. Readily available NaSH served as the
描述了用于合成硫代酰胺和伯硫代酰胺的环保型 ynamide 介导的单硫代羧酸与胺或氢氧化铵的硫代酰胺化反应。简单温和的反应条件使反应能够耐受多种官能团,例如羟基、酯、叔胺、酮和酰胺部分。现成的 NaSH 作为硫源,避免使用有毒、昂贵和恶臭的有机硫试剂,使该策略对环境友好且实用。重要的是,α-手性单硫代羧酸的立体化学完整性在活化步骤和随后的氨解过程中得以保持,从而为肽 C 末端修饰提供了一种无外消旋化策略。此外,
A tris-type iridium complex in which a ligand having a distinctive nitrogen-containing five-membered heterocyclic skeleton is coordinated is provided. The ligand has a nitrogen-containing five-membered heterocyclic skeleton composed of 2 to 4 nitrogen atoms and one or more carbon atoms. In the skeleton, an aryl group is bonded to a carbon atom on both sides of which nitrogen atoms are positioned, and a tricycloalkyl group having a bridge structure and having 9 or 10 carbon atoms is bonded to one of the two nitrogen atoms positioned on both the sides of the carbon atom. The tricycloalkyl group having a bridge structure and having 9 or 10 carbon atoms may be an adamantyl group or a noradamantyl group.