Journal
CHEMICAL COMMUNICATIONS
Volume -, Issue 15, Pages 1708-1709Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/b407324j
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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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