Serviou Stamatis K, Gkizis Petros L, Sánchez Darío Puchán, Plassais Nathan, Gohier Frédéric, Cabanetos Clement, Kokotos Christoforos G
Laboratory of Organic Chemistry, Department of Chemistry, National and Kapodistrian University of Athens, Panepistimiopolis, 15771, Athens, Greece.
CNRS, MOLTECH-ANJOU, SFR-MATRIX, F-49000, Angers, France.
ChemSusChem. 2024 Dec 6;17(23):e202400903. doi: 10.1002/cssc.202400903. Epub 2024 Aug 12.
The sulfoxide moiety is one of the most commonly utilized groups in pharmaceutical and industrial chemistry. The need for sustainability and easy accessibility to sulfoxide moieties is deemed necessary, due to its ubiquity in natural products and potentially pharmaceutically active compounds. In this context, we report herein a sustainable, aerobic and environmentally friendly photochemical protocol based on the use of a benzothioxathene imide as the photocatalyst to selectively oxidize sulfides under mild irradiation (456 nm), in very low catalyst loading (0.01 mol %) and on water. In addition, to demonstrate the compatibility of our protocol with wide scope of substrates, the latter was successfully applied to the synthesis of the biologically-active Sulforaphane and Modafinil.
亚砜基团是药物化学和工业化学中最常用的基团之一。由于其在天然产物和潜在的药物活性化合物中普遍存在,因此对亚砜基团的可持续性和易于获取性的需求被认为是必要的。在此背景下,我们在此报告一种基于使用苯并噻吨酰亚胺作为光催化剂的可持续、有氧且环境友好的光化学方法,该方法在温和照射(456 nm)下、以非常低的催化剂负载量(0.01 mol%)且在水相中选择性氧化硫化物。此外,为了证明我们的方法与广泛的底物具有兼容性,该方法已成功应用于生物活性化合物萝卜硫素和莫达非尼的合成。