催化作用
对映选择合成
模块化(生物学)
组合化学
化学
有机化学
纳米技术
材料科学
生物
遗传学
作者
Takuya Hashimoto,Yuto Shimazaki,Yamato Omatsu,Keiji Maruoka
标识
DOI:10.1002/anie.201803889
摘要
Rapid development in the last decade has rendered chiral organoiodine(I/III) catalysis a reliable methodology in asymmetric catalysis. However, due to the severely limited numbers of effective organoiodine catalysts, many reactions still give low to modest enantioselectivity. We report herein a solution to this issue through the introduction of a pivotal indanol scaffold to the catalyst design. Our catalyst architecture exhibits the advantage of high modularity and thereby expedites catalyst optimization. The catalyst was optimized for the challenging and highly sought-after hydrative dearomatization of 2-substituted phenols at the 4-position.
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