Literature DB >> 14748602

Synthesis of ether oligomers.

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.

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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


  2 in total

1.  In Vivo Chemiluminescent Imaging Agents for Nitroreductase and Tissue Oxygenation.

Authors:  Jian Cao; James Campbell; Li Liu; Ralph P Mason; Alexander R Lippert
Journal:  Anal Chem       Date:  2016-04-15       Impact factor: 6.986

2.  A Rational Active-Site Redesign Converts a Decarboxylase into a C=C Hydratase: "Tethered Acetate" Supports Enantioselective Hydration of 4-Hydroxystyrenes.

Authors:  Stefan E Payer; Hannah Pollak; Silvia M Glueck; Kurt Faber
Journal:  ACS Catal       Date:  2018-02-07       Impact factor: 13.084

  2 in total

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