| Literature DB >> 21957886 |
Darci J Trader1, Erin E Carlson.
Abstract
Although the carboxylic acid moiety is prevalent in many biologically produced molecules, including natural products and proteins, methods to chemoselectively target this functional group have remained elusive. Generally, strategies that utilize carboxylate nucleophilicity also promote reactions with other nucleophiles such as amines and hydroxyls. A reagent was sought to facilitate the selective isolation of carboxylic acid containing compounds from complex mixtures. Here, the development of siloxyl ether functionalized solid supports is described.Entities:
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Year: 2011 PMID: 21957886 PMCID: PMC3215773 DOI: 10.1021/ol202376m
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005