立体中心
替代(逻辑)
磷
亲核取代
催化作用
中心(范畴论)
化学
立体化学
药物化学
结晶学
有机化学
对映选择合成
计算机科学
程序设计语言
作者
Bingbing Dong,Junmin Zhang,Xiang-Yu Ye,Xuan Huang,Yonggui Robin
标识
DOI:10.1016/j.cclet.2025.111052
摘要
P-stereogenic compounds play pivotal roles in natural products, pharmaceuticals, bioactive molecules, and catalysts/ligands, making their synthesis a highly researched area. Current studies have predominantly concentrated on fully carbon-substituted P-stereogenic species, despite the fact that many therapeutically relevant compounds feature P-O, P-N, or P-S bonds. The catalytic and stereoselective nucleophilic substitution at the P-center is acknowledged as a highly efficient and straightforward approach for constructing high-value P-stereogenic compounds, offering significant potential for further development. This review provides an overview of advancements in the construction of P-stereogenic centers based on P-centered nucleophilic substitution, highlighting key challenges, breakthroughs, and future opportunities in the field. High-value P-stereogenic compounds have become a focus of interest for researchers. The catalytic and stereoselective nucleophilic substitution at the P-center is acknowledged as a highly efficient and straightforward approach for constructing high-value P-stereogenic compounds, offering significant potential for further development. This review explores the progress in the construction of P-stereogenic centers based on P-centered nucleophilic substitution, highlighting key challenges, breakthroughs, and future opportunities in the field.
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