首页> 外文期刊>Frontiers in Chemistry >Direct and Efficient C(sp3)–H Functionalization of N-Acyl/Sulfonyl Tetrahydroisoquinolines (THIQs) With Electron-Rich Nucleophiles via 2,3-Dichloro-5,6-Dicyano-1,4-Benzoquinone (DDQ) Oxidation
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Direct and Efficient C(sp3)–H Functionalization of N-Acyl/Sulfonyl Tetrahydroisoquinolines (THIQs) With Electron-Rich Nucleophiles via 2,3-Dichloro-5,6-Dicyano-1,4-Benzoquinone (DDQ) Oxidation

机译:通过2,3-二氯-5,6-二氰基-1,4-苯醌(DDQ)氧化,通过2,3-二氯-5,6-二氰基 - 1,4-苯并醌(DDQ)氧化,直接和高效的C(SP3)-H官能化(Thiqs)用电子富核试剂

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摘要

A highly efficient metal-free oxidative direct C(sp3)–H functionalization of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines (THIQs) with a wide range of electron-rich nucleophiles was accomplished under mild conditions through oxidation with DDQ and subsequent trapping of the resulting reactive and stable N-acyl/sulfonyl iminium ions. The synthetic utility of this method was illustrated by a concise and efficient total synthesis of (±)-benzo[a]quinolizidine (11) in 3 steps from the known N-Cbz-1,2,3,4-THIQ 4b.
机译:通过氧化在温和条件下,通过氧化在温和条件下在温和的条件下完成高效的无金属氧化直接C(SP3)-H官能化的N-酰基/磺酰基1,2,3,4-四羟异喹啉(Thiqs),通过氧化在温和条件下完成DDQ和随后捕获所得反应性和稳定的N-酰基/磺酰亚胺离子。该方法的合成效用通过简明且有效的总合成(±)-benzo [a]喹硫啉(11),从已知的N-CBZ-1,2,3,4-Thiq 4b中的3步骤中的3步骤说明。

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