Department of Optical Nanoscopy, Max Planck Institute for Medical Research, Jahnstrasse 29, 69120 Heidelberg, Germany.
Org Lett. 2021 Apr 2;23(7):2604-2609. doi: 10.1021/acs.orglett.1c00512. Epub 2021 Mar 15.
A modular synthetic approach toward diverse analogues of the far-red fluorophore silicon-rhodamine (SiR), based on a regioselective double nucleophilic addition of aryllanthanum reagents to esters, anhydrides, and lactones, is proposed. The reaction has improved functional group tolerance and represents a unified strategy toward cell-permeant, spontaneously blinking, and photoactivatable SiR fluorescent labels. In tandem with Pd-catalyzed hydroxy- or aminocarbonylation, it serves a streamlined synthetic pathway to a series of validated live-cell-compatible fluorescent dyes.
提出了一种基于芳基金属试剂对酯、酸酐和内酯的区域选择性双亲核加成的、用于合成远红荧光硅罗丹明(SiR)类似物的模块化合成方法。该反应提高了对功能基团的耐受性,为具有细胞通透性、自发闪烁和光活化能力的 SiR 荧光标记物提供了一种统一的策略。与 Pd 催化的羟(氨)羰基化反应相结合,它为一系列经验证的可用于活细胞的荧光染料提供了一条简化的合成途径。