对映选择合成
卡宾
催化作用
膨胀的
化学
基质(水族馆)
分子间力
组合化学
有机化学
材料科学
分子
抗压强度
海洋学
复合材料
地质学
作者
Chong‐Yang Shi,Guangyu Zhu,Yin Xu,Ming‐Yu Teng,Long‐Wu Ye
标识
DOI:10.1016/j.cclet.2023.108441
摘要
Büchner reaction, as a unique type of expansive dearomatization, has become a practical strategy for the straightforward assembly of valuable functionalized cycloheptatrienes from ubiquitous aromatic precursors. Although the asymmetric version has been investigated since the early 1990s, enantioselective Büchner reaction is still limited by the catalyst type and substrate scope. This review aims to propose the limitation and possible development direction of this field by summarizing the evolution of catalytic asymmetric Büchner reaction, which is organized on the basis of intra- and intermolecular reactions. Considering the different metal carbene precursors, the reactions are further classified by carbene sources.
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