1. Synthesis of spirocyclic scaffolds using hypervalent iodine reagents
- Author
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Samata E. Shetgaonkar, Fateh V. Singh, Saeesh R. Mangaonkar, and Priyanka B. Kole
- Subjects
natural products ,chemistry.chemical_element ,Review ,010402 general chemistry ,Iodine ,oxidative cyclization ,01 natural sciences ,iodoarenes ,Catalysis ,lcsh:QD241-441 ,chemistry.chemical_compound ,lcsh:Organic chemistry ,hypervalent iodine reagents ,lcsh:Science ,Natural product ,spirocyclic compounds ,010405 organic chemistry ,Chemistry ,Organic Chemistry ,Hypervalent molecule ,Heavy metals ,Combinatorial chemistry ,0104 chemical sciences ,Reagent ,lcsh:Q ,Organic synthesis ,Stereoselectivity - Abstract
Hypervalent iodine reagents have been developed as highly valuable reagents in synthetic organic chemistry during the past few decades. These reagents have been identified as key replacements of various toxic heavy metals in organic synthesis. Various synthetically and biologically important scaffolds have been developed using hypervalent iodine reagents either in stoichiometric or catalytic amounts. In addition, hypervalent iodine reagents have been employed for the synthesis of spirocyclic scaffolds via dearomatization processes. In this review, various approaches for the synthesis of spirocyclic scaffolds using hypervalent iodine reagents are covered including their stereoselective synthesis. Additionally, the applications of these reagents in natural product synthesis are also covered.
- Published
- 2018
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