| Literature DB >> 14748602 |
Olivier Renaudet1, Jean-Louis Reymond.
Abstract
[structure: see text] Hydroxyaromatic aldehydes and ketones were used as building blocks to prepare ether oligomers. An iterative two-step protocol involving Mitsunobu coupling and carbonyl reduction provided a protecting-group-free route with high yields. Activity screening of an 84-member library against proteases led to the discovery of micromolar inhibitors for trypsin, chymotrypsin, and subtilisin.Entities:
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Year: 2004 PMID: 14748602 DOI: 10.1021/ol036300d
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005