| Literature DB >> 19354277 |
Jan Kocí1, Nadĕzda Pudelová, Viktor Krchnák.
Abstract
Polymer-supported alpha-acylamino ketones were prepared from resin-bound amines, bromoketones, and carboxylic acids. Selective monoalkylation of amines by bromoketones was carried out via 4-nitrobenzenesulfonamides. There was a striking difference in the reaction outcome between 2-Nos and 4-Nos derivatives. Alpha-acylamino ketones were converted to imidazoles. The cyclization was performed on resin, allowing further polymer-supported elaboration of imidazoles including synthesis of bis-heterocyclic compounds. A small combinatorial array of imidazoles was synthesized. Target compounds were prepared under mild conditions using commercially available building blocks for the introduction of three points of diversity.Entities:
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Year: 2009 PMID: 19354277 PMCID: PMC2733363 DOI: 10.1021/cc800210q
Source DB: PubMed Journal: J Comb Chem ISSN: 1520-4766