天然产物
反应性(心理学)
自然(考古学)
群众
产品(数学)
全合成
生化工程
有机合成
化学
有机化学
计算机科学
组合化学
工程类
生物
数学
哲学
医学
认识论
古生物学
催化作用
病理
替代医学
几何学
作者
Caroline Grundke,Nina Vierengel,Till Opatz
标识
DOI:10.1002/tcr.202000066
摘要
Due to their numerous reactivity modes, α-aminonitriles represent versatile and valuable building blocks in organic total synthesis. Since their discovery by Adolph Strecker in 1850, this compound class has seen a wide dissemination in synthetic applications from laboratory to million-ton industrial scale and was extensively used in the syntheses of various classes of natural products. As these compounds provide a multitude of reactivity options, we feel that a broad overview of their multiple reaction modes may reveal less familiar opportunities for successful total synthesis planning. This personal account article will thus focus on α-aminonitriles used as key intermediates in selected natural product synthesis sequences which have been reported in the two decades since Enders' and Shilvock's seminal review. Natural α-aminonitriles will also briefly be treated.
科研通智能强力驱动
Strongly Powered by AbleSci AI