Catalytic construction of P-stereogenic center via phosphorus-centered nucleophilic substitution

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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Publication Details

Journal
Chinese Chemical Letters
Published
2025-03-07
DOI
https://doi.org/10.1016/j.cclet.2025.111052
Citations
5
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
2.69

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article

Catalytic construction of P-stereogenic center via phosphorus-centered nucleophilic substitution

Bingbing Dong, Yonggui Robin, Xuan Huang, Junmin Zhang et al.
5 citations
Chinese Chemical Letters
Asymmetric Hydrogenation and Catalysis
2.69
article

Catalytic construction of P-stereogenic center via phosphorus-centered nucleophilic substitution

Bingbing Dong, Yonggui Robin, Xuan Huang, Junmin Zhang, Xiang-Yu Ye
article en
5 citations

Abstract

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.

Chinese Chemical LettersVol. 36(9)
Nanyang Technological University (SG), Guizhou University (CN), Shenzhen University (CN)
Science and Technology Foundation of Shenzhen City, National Research Foundation Singapore, Ministry of Education - Singapore, Nanyang Technological University, National Natural Science Foundation of China, National Research Foundation of Korea, Department of Education of Guangdong Province, Department of Education of Guizhou Province
Openalex Percentile: Top 11%
Asymmetric Hydrogenation and Catalysis
2.69
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