TY - JOUR
T1 - Recent advances in ligand-enabled palladium-catalyzed divergent synthesis
AU - Wang, Yue
AU - Feng, Jinzan
AU - Li, Er Qing
AU - Jia, Zhenhua
AU - Loh, Teck Peng
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2023/11/27
Y1 - 2023/11/27
N2 - Developing efficient and straightforward strategies to rapidly construct structurally distinct and diverse organic molecules is one of the most fundamental tasks in organic synthesis, drug discovery and materials science. In recent years, divergent synthesis of organic functional molecules from the same starting materials has attracted significant attention and has been recognized as an efficient and powerful strategy. To achieve this objective, the proper adjustment of reaction conditions, such as catalysts, solvents, ligands, etc., is required. In this review, we summarized the recent efforts in chemo-, regio- and stereodivergent reactions involving acyclic and cyclic systems catalyzed by palladium complexes. Meanwhile, the reaction types, including carbonylative reactions, coupling reactions and cycloaddition reactions, as well as the probable mechanism have also been highlighted in detail.
AB - Developing efficient and straightforward strategies to rapidly construct structurally distinct and diverse organic molecules is one of the most fundamental tasks in organic synthesis, drug discovery and materials science. In recent years, divergent synthesis of organic functional molecules from the same starting materials has attracted significant attention and has been recognized as an efficient and powerful strategy. To achieve this objective, the proper adjustment of reaction conditions, such as catalysts, solvents, ligands, etc., is required. In this review, we summarized the recent efforts in chemo-, regio- and stereodivergent reactions involving acyclic and cyclic systems catalyzed by palladium complexes. Meanwhile, the reaction types, including carbonylative reactions, coupling reactions and cycloaddition reactions, as well as the probable mechanism have also been highlighted in detail.
UR - http://www.scopus.com/inward/record.url?scp=85179161293&partnerID=8YFLogxK
U2 - 10.1039/d3ob01679j
DO - 10.1039/d3ob01679j
M3 - 文献综述
C2 - 38050418
AN - SCOPUS:85179161293
SN - 1477-0520
VL - 22
SP - 37
EP - 54
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
IS - 1
ER -