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            An efficient iodine pentoxide-triggered iodocarbocyclizations for the synthesis of iodooxindoles in water

            An efficient iodocarbocyclization of alkenes for the synthesis of iodooxindoles has been developed. This reaction proceeds in a chemoselective manner and shows excellent tolerance of various functional groups, including a chemosensitive hydroxymethyl group. Nonmetal inorganic iodine pentoxide was used as bot Synthetic methodology in OBC

            Authors:   Ming-Zhong Zhang; Xin Wang; Ming-Ying Gong; Lin Chen; Wenbin Shi; Shu-Hua He; Yong Jiang; Tieqiao Chen
            Journal:   Organic & Biomolecular Chemistry
            DOI:   10.1039/C8OB01130C
            Facts, background information, dossiers
            • functional groups
            • alkenes
            More about RSC Publishing
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