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Metal-Free Hydrogenation Catalyzed by an Air-Stable Borane: Use of Solvent as a Frustrated Lewis Base
被引:95
|作者:
Scott, Daniel J.
[1
]
Fuchter, Matthew J.
[1
]
Ashley, Andrew E.
[1
]
机构:
[1] Univ London Imperial Coll Sci Technol & Med, Dept Chem, London SW7 2AZ, England
基金:
英国工程与自然科学研究理事会;
关键词:
boranes;
frustrated Lewis pairs;
heterocycles;
hydrogenation;
solvent effects;
SMALL-MOLECULE ACTIVATION;
B(C6F5)(3)-CATALYZED HYDROSILATION;
ALKENE POLYMERIZATION;
PAIRS;
DIHYDROGEN;
IMINES;
ETHERS;
THF;
TETRAHYDROFURAN;
REACTIVITY;
D O I:
10.1002/anie.201405531
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
In recent years 'frustrated Lewis pairs' (FLPs) have been shown to be effective metal-free catalysts for the hydrogenation of many unsaturated substrates. Even so, limited functional-group tolerance restricts the range of solvents in which FLP-mediated reactions can be performed, with all FLP-mediated hydrogenations reported to date carried out in non-donor hydrocarbon or chlorinated solvents. Herein we report that the bulky Lewis acids B(C6Cl5)(x)(C6F5)(3-x) (x= 0-3) are capable of heterolytic H-2 activation in the strong-donor solvent THF, in the absence of any additional Lewis base. This allows metal-free catalytic hydrogenations to be performed in donor solvent media under mild conditions; these systems are particularly effective for the hydrogenation of weakly basic substrates, including the first examples of metal-free catalytic hydrogenation of furan heterocycles. The air-stability of the most effective borane, B(C6Cl5)(C6F5)(2), makes this a practically simple reaction method.
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页码:10218 / 10222
页数:5
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