Duangkamol Chuthamat, Batsomboon Paratchata, Stiegman Albert E, Dudley Gregory B
C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, WV, 26505, USA.
Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL, 32306, USA.
Chem Asian J. 2019 Aug 1;14(15):2594-2597. doi: 10.1002/asia.201900625. Epub 2019 Jun 26.
Microwave (MW) heating is more effective than conventional (CONV) heating for promoting a high-temperature oxidative cycloisomerization reaction that was previously reported as a key step in a total synthesis of the natural product illudinine. The thermal reaction pathway as envisioned is an inverse electron-demand dehydro-Diels-Alder reaction with in situ oxidation to generate a substituted isoquinoline, which itself is unstable to the reaction conditions. Observed reaction yields were higher at a measured bulk temperature of 200 °C than at 180 °C or 220 °C; at 24 hours than at earlier or later time points; and when the reaction solution was heated using MW energy as opposed to CONV heating with a metal heat block. Selective MW heating of polar solute aggregates is postulated to explain these observations.
微波(MW)加热在促进高温氧化环异构化反应方面比传统(CONV)加热更有效,该反应先前被报道为天然产物伊利丁宁全合成中的关键步骤。设想的热反应途径是一个逆电子需求的脱氢狄尔斯-阿尔德反应,伴随原位氧化以生成取代异喹啉,而该取代异喹啉本身对反应条件不稳定。在测量的本体温度为200°C时观察到的反应产率高于180°C或220°C时;在24小时时高于更早或更晚的时间点;并且当使用MW能量加热反应溶液时,产率高于使用金属加热块进行CONV加热时。推测极性溶质聚集体的选择性MW加热可以解释这些观察结果。