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Nickel-Catalyzed Direct Alkylation of Terminal Alkynes at Room Temperature: A Hemilabile Pincer Ligand Enhances Catalytic Activity
被引:78
作者:
Garcia, Pablo M. Perez
[1
]
Ren, Peng
[1
]
Scopelliti, Rosario
[1
]
Hu, Xile
[1
]
机构:
[1] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, Lab Inorgan Synth & Catalysis, EPFL ISIC LSCI, CH-1015 Lausanne, Switzerland
基金:
瑞士国家科学基金会;
关键词:
nickel;
Sonogashira coupling alkynylation;
pincer complex;
kinetics;
alkylation;
BIMETALLIC OXIDATIVE ADDITION;
GRIGNARD-REAGENTS;
HALIDES;
COMPLEXES;
NI;
ARYL;
METHODOLOGY;
BROMIDES;
PD;
D O I:
10.1021/cs501502u
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Direct coupling of alkyl halides with terminal alkynes provides an efficient and streamlined access to alkyl-substituted alkynes, which are important synthetic intermediates, biologically active molecules, and organic materials. However, until now,there have been fewer than a handful of catalytic methods available for this reaction, and detailed mechanistic studies have not been reported. Herein, we describe the design and development a new nickel pincer complex that catalyzes the direct coupling of primary alkyl halides with terminal alkynes at room temperature. The catalysis has a good substrate scope and high functional group tolerance. Kinetic data suggest that the new pincer ligand is hemilabile, and the dissociation of a labile amine donor is the (t)urnover-determining step of the catalysis. An intermediate Ni-alkynyl species has been isolated and structurally characterized. The reactivity of this species gives insight into the nature of the active species for the activation of alkyl halide.
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页码:1164 / 1171
页数:8
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