Arunkirirote Piyaporn, Suwalak Pornteera, Chaisan Nattawadee, Tummatorn Jumreang, Ruchirawat Somsak, Thongsornkleeb Charnsak
Laboratory of Medicinal Chemistry, Chulabhorn Research Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand.
Program on Chemical Sciences, Chulabhorn Graduate Institute, 54 Kamphaeng Phet 6, Laksi, Bangkok 10210, Thailand.
Org Lett. 2024 Nov 1;26(43):9173-9178. doi: 10.1021/acs.orglett.4c02708. Epub 2024 Aug 30.
A photochemical Machetti-De Sarlo reaction has been developed for preparing 5-substituted 3-acylisoxazoles from acylnitromethanes and terminal alkynes. This photochemical protocol utilizes an innovative electron donor-acceptor complex, generated from acylnitromethanes, catalytic LiOBu, and 1,1,1,3,3,3-hexafluoro-2-propanol, as a photosensitizer to promote rapid conversion with a broad substrate scope in up to 80% efficiency. A sigmoidal autoinductive kinetic profile is revealed, demonstrating the novel and unique dual catalysis in the first photochemical approach of this reaction.
已开发出一种光化学马凯蒂-德萨洛反应,用于从酰基硝基甲烷和末端炔烃制备5-取代的3-酰基异恶唑。这种光化学方法利用了一种创新的电子供体-受体络合物,该络合物由酰基硝基甲烷、催化量的丁基锂和1,1,1,3,3,3-六氟-2-丙醇生成,作为光敏剂,以高达80%的效率促进广泛底物范围的快速转化。揭示了一种S形自诱导动力学曲线,证明了该反应首次光化学方法中新颖独特的双催化作用。