TY - JOUR
T1 - Recent applications of axially chiral skeletons in asymmetric catalysis
AU - Jiang, Peng Ying
AU - Wu, San
AU - Xiang, Shao Hua
AU - Chen, Pengquan
AU - Wang, Jun (Joelle)
AU - Tan, Bin
N1 - We are grateful for financial support from the National Natural Science Foundation of China ( 22425011 , 22231004 , 22271135 , 22401135 , and 22501129 ); the National Key R&D Program of China ( 2022YFA1503700 ); the Research Grants Council of Hong Kong ( SRFS2526-2S02 ); the Hong Kong Scholars Program ( XJ2024-007 ); the Guangdong Basic and Applied Basic Research Foundation ( 2024B1515020055 ); the New Cornerstone Science Foundation through the Xplorer Prize; the Shenzhen Science and Technology Program ( KQTD20210811090112004 ); and High level of special funds ( G03050K003 ).
Publisher Copyright:
© 2026 Elsevier Inc.
PY - 2026/8/13
Y1 - 2026/8/13
N2 - Axially chiral skeletons provide a molecular foundation for constructing chiral environments in asymmetric catalysis by leveraging their rigid conformational architectures and tunable electronic properties. This perspective systematically elucidates the applications of such skeletons, from metal ligands to organocatalysts, through representative case studies. In metal catalysis, coordination with diverse metal centers enables efficient asymmetric induction. In organocatalysis, mechanisms such as hydrogen bonding and ion pairing allow direct substrate activation and stereochemical control. Notably, their applications in cooperative catalysis and photo-/electrocatalysis have led to breakthroughs in stereodiscrimination of highly reactive intermediates, expanding the frontiers of asymmetric synthesis. Future developments in this field will focus on function-oriented catalyst design, innovations in photo-/electrocatalytic systems, and industrial translation, thereby providing sustained driving force for the precise construction of complex chiral molecules.
AB - Axially chiral skeletons provide a molecular foundation for constructing chiral environments in asymmetric catalysis by leveraging their rigid conformational architectures and tunable electronic properties. This perspective systematically elucidates the applications of such skeletons, from metal ligands to organocatalysts, through representative case studies. In metal catalysis, coordination with diverse metal centers enables efficient asymmetric induction. In organocatalysis, mechanisms such as hydrogen bonding and ion pairing allow direct substrate activation and stereochemical control. Notably, their applications in cooperative catalysis and photo-/electrocatalysis have led to breakthroughs in stereodiscrimination of highly reactive intermediates, expanding the frontiers of asymmetric synthesis. Future developments in this field will focus on function-oriented catalyst design, innovations in photo-/electrocatalytic systems, and industrial translation, thereby providing sustained driving force for the precise construction of complex chiral molecules.
KW - asymmetric catalysis
KW - axially chiral skeletons
KW - catalyst
KW - ligand
UR - https://www.scopus.com/pages/publications/105046793546
UR - https://www.sciencedirect.com/science/article/abs/pii/S2451929426002536?via%3Dihub
U2 - 10.1016/j.chempr.2026.103187
DO - 10.1016/j.chempr.2026.103187
M3 - Journal article
AN - SCOPUS:105046793546
SN - 2451-9308
VL - 12
JO - Chem
JF - Chem
IS - 8
M1 - 103187
ER -