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Synthesis and Functionalization of S-heterocycles via CDC Reactions

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Heterocycles via Cross Dehydrogenative Coupling

Abstract

Cross-dehydrogenative coupling has become a powerful tool in organic synthesis. The current developments in the assembly and functionalization of S-heterocycles using this strategy are highlighted in this chapter. The preparation of benzothiophenes, benzothiazoles and cyclic sultams and sulfoxides by intramolecular C(sp2)–H/S–H and C(sp2)–H/C(sp2)–H coupling is discussed. In addition, the coupling of S-heterocycles to arenes and aliphatic compounds is also presented.

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  1. Department of Chemistry, The University of the West Indies, Mona, Kingston 7, Jamaica

    Nadale K. Downer-Riley

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Correspondence to Nadale K. Downer-Riley .

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  1. National Institute of Pharmaceutical Education and Research, Guwahati, Assam, India

    Ananya Srivastava

  2. Indian Institute of Technology Guwahati, Guwahati, Assam, India

    Chandan K. Jana

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Downer-Riley, N.K. (2019). Synthesis and Functionalization of S-heterocycles via CDC Reactions. In: Srivastava, A., Jana, C. (eds) Heterocycles via Cross Dehydrogenative Coupling. Springer, Singapore. https://doi.org/10.1007/978-981-13-9144-6_8

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