Matches in UGent Biblio for { <https://biblio.ugent.be/publication/2045513#aggregation> ?p ?o. }
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- aggregation classification "A1".
- aggregation creator B445328.
- aggregation creator B445329.
- aggregation creator B445330.
- aggregation creator B445331.
- aggregation creator B445332.
- aggregation creator B445333.
- aggregation creator person.
- aggregation date "2011".
- aggregation hasFormat 2045513.bibtex.
- aggregation hasFormat 2045513.csv.
- aggregation hasFormat 2045513.dc.
- aggregation hasFormat 2045513.didl.
- aggregation hasFormat 2045513.doc.
- aggregation hasFormat 2045513.json.
- aggregation hasFormat 2045513.mets.
- aggregation hasFormat 2045513.mods.
- aggregation hasFormat 2045513.rdf.
- aggregation hasFormat 2045513.ris.
- aggregation hasFormat 2045513.txt.
- aggregation hasFormat 2045513.xls.
- aggregation hasFormat 2045513.yaml.
- aggregation isPartOf urn:issn:0039-7881.
- aggregation language "eng".
- aggregation subject "Chemistry".
- aggregation title "Diversity-oriented silver(I)-mediated synthesis of spiro-2-aminoimidazoles".
- aggregation abstract "A diversity-oriented protocol giving access to a novel class of spiro-cyclic guanidine derivatives is described. The copper( I)-catalyzed, three-component coupling of a ketone, an alkyne and a primary amine (KA(2)-coupling) provides the required secondary propargylamines and assures the generation of diversity. The key step of the protocol, a silver(I)-mediated tandem guanylation of secondary propargylamines followed by an intramolecular heterocyclization, provides the target bis-Boc-protected-2-iminoimidazolines spiro-fused with a five-, six- or seven-membered (heterocyclic) ring, which could, in most cases, be further deprotected to the spiro-2-aminoimidazoles.".
- aggregation authorList BK777690.
- aggregation endPage "1594".
- aggregation issue "10".
- aggregation startPage "1587".
- aggregation isDescribedBy 2045513.
- aggregation similarTo s-0030-1260012.
- aggregation similarTo LU-2045513.