Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5268696 | Tetrahedron Letters | 2015 | 4 Pages |
Abstract
A glucose-containing imidazolium salt β-1-imidazole-2,3,4,6-tetraacetyl-D-glucopyranosyl bromide was firstly used as efficient noncovalent organocatalyst to promote the solvent-free preparation of ortho-aminocarbonitriles via a four-component condensation of aromatic aldehyde, cyclohexanone, and 2 equiv of malononitrile at room temperature. Seven bonds were cleaved while four new bonds were formed and a six-membered ring was constructed in one-pot.
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