立体中心
催化作用
拓扑(电路)
基质(水族馆)
羟醛反应
化学
组合化学
立体化学
对映选择合成
有机化学
数学
组合数学
生物
生态学
作者
Dominik Lotter,Alessandro Castrogiovanni,Markus Neuburger,Christof Sparr
标识
DOI:10.1021/acscentsci.8b00204
摘要
Molecular scaffolds with multiple rotationally restricted bonds allow a precise spatial positioning of functional groups. However, their synthesis requires methods addressing the configuration of each stereogenic axis. We report here a catalyst-stereocontrolled synthesis of atropisomeric multiaxis systems enabling divergence from the prevailing stereochemical reaction path. By using ion-pairing catalysts in arene-forming aldol condensations, a strong substrate-induced stereopreference can be overcome to provide structurally well-defined helical oligo-1,2-naphthylenes. The configuration of up to four stereogenic axes was individually catalyst-controlled, affording quinquenaphthalenes with a unique topology.
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