Jadala Chetna, Prasad Budaganaboyina, Prasanthi A V G, Shankaraiah Nagula, Kamal Ahmed
Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER) Hyderabad-500 037 India
Medicinal Chemistry & Pharmacology, CSIR-Indian Institute of Chemical Technology Hyderabad 500 007 India
RSC Adv. 2019 Sep 27;9(53):30659-30665. doi: 10.1039/c9ra06778g. eCollection 2019 Sep 26.
A mild and metal-free one-pot synthetic strategy has been developed for the construction of substituted pyrroles by employing aza-Wittig reaction from a unique and unexplored combination of chromones and phenacyl azides. This method does not compromise the diverse substitutions on both the phenacyl azides and chromones. The merits of this method are wide substrate scope, easy functionalization, short reaction time, operationally simple, and higher yields. Moreover, this method is amenable for the generation of a library of key pyrrole building blocks.
通过使用色酮和苯甲酰叠氮化物这一独特且未被探索的组合进行氮杂维蒂希反应,已开发出一种温和且无金属的一锅法合成策略,用于构建取代吡咯。该方法不会影响苯甲酰叠氮化物和色酮上的多种取代基。此方法的优点包括底物范围广、易于官能化、反应时间短、操作简单且产率较高。此外,该方法适用于生成关键吡咯结构单元的文库。