A Synthesis of novelIH-Imidazo[1,2-α]Indole-3-Carboxylates
摘要:
A route to the uncommon imidazo[1,2-a]indole nucleus 1 is described via functionalisation and annelation of readily accessible 2-amino-indole-3-carboxylates 5. Intramolecular cyclization of a key 2-indolylformamidate 6 was utilised for the preparation of the 3,9-diester intermediates 7.
Preparation of a Novel pH-responsive Fluorescent Probe Based on an Imidazo[1,2-a]indole Fluorophore and its Application in Detecting Extremely Low pH in Saccharomyces cerevisiae
A Synthesis of novel<i>IH</i>-Imidazo[1,2-α]Indole-3-Carboxylates
作者:Ian T. Forbes、Helen K.A. Morgan、Mervyn Thompson
DOI:10.1080/00397919608086749
日期:1996.2
A route to the uncommon imidazo[1,2-a]indole nucleus 1 is described via functionalisation and annelation of readily accessible 2-amino-indole-3-carboxylates 5. Intramolecular cyclization of a key 2-indolylformamidate 6 was utilised for the preparation of the 3,9-diester intermediates 7.
Preparation of a Novel pH-responsive Fluorescent Probe Based on an Imidazo[1,2-a]indole Fluorophore and its Application in Detecting Extremely Low pH in Saccharomyces cerevisiae
作者:Yanhao Xu、Ruikang Duan、Hao Liu、Chengcai Xia、Guiyun Duan、Yanqing Ge
DOI:10.1007/s10895-021-02739-8
日期:2021.9
A novel pH-responsive probe based on an imidazo[1,2-a]indole fluorophore architecture is reported. The probe was highly selective to strongly acidic pH (pKa = 3.56) with high sensitivity and a fast response time (within 30 s). The probe did not demonstrate any fluorescence changes in the presence of interfering metal ions, and it featured excellent reversibility under strongly acidic conditions. The mechanism of detection of the probe was determined to be based on intramolecular charge transfer (ICT) at different pH. The probe was also able to be used for imaging for detecting acidic pH in Saccharomyces cerevisiae.