磺酰自由基加成-环化及其合成应用

Okiko Miyata, Takeaki Naito
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引用次数: 1

摘要

本文综述了一种基于磺胺基自由基加成-环化的新型高效碳-碳成键反应,这种反应是由磺胺基自由基加成到多键上形成碳中心自由基,然后在分子内将碳中心自由基加成到多键上。通过合成安antine、氧对苯内酯、顺戊酸、维生素D和α-kainic酸,证明了该化合物的合成潜力。
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Sulfanyl radical addition–cyclization and its synthetic application

This review summarizes a new efficient carbon–carbon bond-forming reaction based on sulfanyl radical addition–cyclization, which proceeds by the formation of a carbon-centered radical species generated by the addition of a sulfanyl radical to a multiple bond and then intramolecular addition of the resulting carbon-centered radical to a multiple bond. The synthetic potentiality was demonstrated by the syntheses of anantine, oxo-parabenzlactone, cispentacin, vitamin D, and α-kainic acid.

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