Ring-Opening Metathesis Polymerization-based Recyclable Magnetic Acylation Reagents

被引:14
|
作者
Kainz, Quirin M. [1 ]
Linhardt, Roland [1 ]
Maity, Pradip K. [2 ]
Hanson, Paul R. [2 ]
Reiser, Oliver [1 ]
机构
[1] Univ Regensburg, Inst Organ Chem, D-93053 Regensburg, Germany
[2] Univ Kansas, Dept Chem, Lawrence, KS 66045 USA
关键词
acylation; metathesis; magnetic nanobeads; polymerization; supported catalyst; CHEMICAL LIBRARY SYNTHESIS; PEPTIDE-SYNTHESIS; ACTIVE ESTERS; SOLID-PHASE; N-HYDROXYSUCCINIMIDE; FUNCTIONAL POLYMERS; PALLADIUM CATALYST; PARALLEL SYNTHESIS; COUPLING REAGENTS; ORGANIC-SYNTHESIS;
D O I
10.1002/cssc.201200453
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An operationally simple method for the acylation of amines utilizing carbon-coated metal nanoparticles as recyclable supports is reported. Highly magnetic carbon-coated cobalt (Co/C) and iron (Fe/C) nanobeads were functionalized with a norbornene tag (Nb-tag) through a click reaction followed by surface activation employing Grubbs-II catalyst and subsequent grafting of acylated N-hydroxysuccinimide ROMPgels (ROMP=ring-opening metathesis polymerization). The high loading (up to 2.6mmolg1) hybrid material was applied in the acylation of various primary and secondary amines. The products were isolated in high yields (8699%) and excellent purities (all >95% by NMR spectroscopy) after rapid magnetic decantation and simple evaporation of the solvents. The spent resins were successfully re-acylated by acid chlorides, anhydrides, and carboxylic acids and reused for up to five consecutive cycles without considerable loss of activity.
引用
收藏
页码:721 / 729
页数:9
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