Chiral Dinucleating Salan-Type Phosphine Ligands for Asymmetric Allylic Alkylations with α-Cyano Ketones

While chiral dinuclear catalysts have emerged as a powerful strategy to overcome the inherent limitations of monometallic systems in terms of stereocontrol and reactivity, the development of chiral dinucleating phosphine ligands has been less explored. Guided by the principle of dinuclear cooperative activation, we developed a new class of chiral dinucleating phosphine ligands based on a salan-type scaffold. The catalytic utility of these ligands was demonstrated through their successful application in a Ni/Pd heterobimetallic system for asymmetric allylic alkylations with α-cyano ketones and esters. This methodology enables the efficient construction of nitrile compounds bearing quaternary stereocenters.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2026-04-01
DOI
https://doi.org/10.1021/acs.orglett.6c01052
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Chiral Dinucleating Salan-Type Phosphine Ligands for Asymmetric Allylic Alkylations with α-Cyano Ketones

Sai Fei Wang, P. N. Li, Yihao Zhang
Organic Letters
Asymmetric Synthesis and Catalysis
article

Chiral Dinucleating Salan-Type Phosphine Ligands for Asymmetric Allylic Alkylations with α-Cyano Ketones

Sai Fei Wang, P. N. Li, Yihao Zhang
article en

Abstract

While chiral dinuclear catalysts have emerged as a powerful strategy to overcome the inherent limitations of monometallic systems in terms of stereocontrol and reactivity, the development of chiral dinucleating phosphine ligands has been less explored. Guided by the principle of dinuclear cooperative activation, we developed a new class of chiral dinucleating phosphine ligands based on a salan-type scaffold. The catalytic utility of these ligands was demonstrated through their successful application in a Ni/Pd heterobimetallic system for asymmetric allylic alkylations with α-cyano ketones and esters. This methodology enables the efficient construction of nitrile compounds bearing quaternary stereocenters.

Organic LettersVol. 28(14)
Quaid-i-Azam University (PK), East China University of Science and Technology (CN)
Shanghai Jiao Tong University, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 28%
Asymmetric Synthesis and Catalysis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Chiral Dinucleating Salan-Type Phosphine Ligands for Asymmetric Allylic Alkylations with α-Cyano Ketones — Sai Fei Wang, P. N. Li, et al. · Organic Letters (2026) | TGRS Research Map | TGRS