Synthesis of 3,4-Dihydro-2H-Pyrroles from Ketones, Aldehydes, and Nitro Alkanes via Hydrogenative Cyclization

被引:4
|
作者
Klausfelder, Barbara [1 ]
Blach, Patricia [2 ,3 ]
de Jonge, Niels [2 ,3 ]
Kempe, Rhett [1 ]
机构
[1] Univ Bayreuth, Sustainable Chem Ctr, Anorgan Chem 2, Catalyst Design, Univ Str 30, D-95440 Bayreuth, Germany
[2] INM Leibniz Inst New Mat, Campus D2 2, D-66123 Saarbrucken, Germany
[3] Saarland Univ, Dept Phys, Campus D2 2, D-66123 Saarbrucken, Germany
关键词
catalysis; hydrogenation; multicomponent reaction; N-heterocycles; nickel; FUNCTIONALIZED PYRIDINES; SELECTIVE HYDROGENATION; GENERAL-SYNTHESIS; PYRROLES; REDUCTION; NANOPARTICLES; CATALYSTS; ALCOHOLS;
D O I
10.1002/chem.202201307
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Syntheses of N-heterocyclic compounds that permit a flexible introduction of various substitution patterns by using inexpensive and diversely available starting materials are highly desirable. Easy to handle and reusable catalysts based on earth-abundant metals are especially attractive for these syntheses. We report here on the synthesis of 3,4-dihydro-2H-pyrroles via the hydrogenation and cyclization of nitro ketones. The latter are easily accessible from three components: a ketone, an aldehyde and a nitroalkane. Our reaction has a broad scope and 23 of the 33 products synthesized are compounds which have not yet been reported. The key to the general hydrogenation/cyclization reaction is a highly active, selective and reusable nickel catalyst, which was identified from a library of 24 earth-abundant metal catalysts.
引用
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页数:7
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