Literature DB >> 15278148

A Suzuki-Miyaura coupling mediated deprotection as key to the synthesis of a fully lipidated malarial GPI disaccharide.

Xinyu Liu1, Peter H Seeberger.   

Abstract

Ligandless palladium-catalyzed Suzuki-Miyaura coupling converted an inert p-bromobenzyl ether to a DDQ-labile p-(3,4-dimethoxyphenyl) benzyl ether in the presence of azide functionality and this strategy serves as a key step for the convergent synthesis of a fully lipidated malaria GPI disaccharide.

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Year:  2004        PMID: 15278148     DOI: 10.1039/b407324j

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  1 in total

1.  Convenient method for preparing benzyl ethers and esters using 2-benzyloxypyridine.

Authors:  Susana S Lopez; Gregory B Dudley
Journal:  Beilstein J Org Chem       Date:  2008-11-26       Impact factor: 2.883

  1 in total

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