Fullerenyl boronic esters have been prepared by a ferric perchlorate-promoted reaction of [60]fullerene with various arylboronic acids. The obtained fullerenyl boronic esters could undergo further functionalization with diols to afford C(60)-fused dioxane/dioxepane derivatives. A possible reaction mechanism for the formation of fullerenyl boronic esters has been proposed.
Organic letters. 2012 Apr 6;14(7):1800-3. doi: 10.1021/ol300398n Q15.02025
Fullerenyl boronic esters: ferric perchlorate-mediated synthesis and functionalization
富勒烯硼酸酯的合成及功能化研究 翻译改进
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DOI: 10.1021/ol300398n PMID: 22416858
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Keywords:fullerenyl boronic esters