Sen Raju, Bhardwaj Srashti, Bar Krishnendu, Deshwal Shalu, Vaitla Janakiram
Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, 110016, India.
Chem Commun (Camb). 2023 Oct 17;59(83):12411-12422. doi: 10.1039/d3cc04137a.
Sulfoxonium ylides are important synthetic precursors in various organic transformations. Their synthetic potential was well explored in the synthesis of various bioactive natural products and pharmaceuticals. Vinyl sulfoxonium ylide is a stabilized sulfoxonium ylide containing an electron-deficient alkene at the ylidic carbon. Similar to α-keto sulfoxonium ylides, these reagents can generate vinyl carbenes in the presence of metals under suitable conditions. These vinyl carbenes can be used for various organic transformations such as X-H (X = C, N, O, S) insertions, annulations, and rearrangement reactions. Due to the dipole structure of the vinyl sulfoxonium ylide, it can undergo electrophilic addition with electrophiles at the α-position. These reagents are used as synthons for various aromatic and heteroaromatic compound syntheses. Moreover, their stability and convenient handling make them potential replacements for thermally less stable vinyl diazo compounds. Herein, we provide an overview of early efforts in this area, with particular emphasis on our own recent development of vinyl sulfoxonium ylide-mediated transformations in the presence and absence of metal catalysis, and also give personal perspectives on the challenges and future scope for improving the application of vinyl sulfoxonium ylides.
硫叶立德是各种有机转化中重要的合成前体。它们的合成潜力在各种生物活性天然产物和药物的合成中得到了充分探索。乙烯基硫叶立德是一种稳定的硫叶立德,在叶立德碳上含有一个缺电子烯烃。与α-酮硫叶立德类似,这些试剂在合适的条件下在金属存在下可以生成乙烯基卡宾。这些乙烯基卡宾可用于各种有机转化,如X-H(X = C、N、O、S)插入、环化和重排反应。由于乙烯基硫叶立德的偶极结构,它可以在α-位与亲电试剂发生亲电加成。这些试剂用作各种芳香族和杂芳香族化合物合成的合成子。此外,它们的稳定性和易于处理使其成为热稳定性较差的乙烯基重氮化合物的潜在替代品。在此,我们概述了该领域的早期努力,特别强调了我们自己最近在有金属催化和无金属催化情况下乙烯基硫叶立德介导的转化方面的进展,并对改善乙烯基硫叶立德应用的挑战和未来前景给出了个人观点。