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Toward the total synthesis of elisapterosin B: a Hg(OTf)2-promoted diastereoselective intramolecular Friedel–Crafts alkylation reaction

✍ Scribed by Weijiang Ying; Charles L. Barnes; Michael Harmata


Publisher
Elsevier Science
Year
2011
Tongue
French
Weight
488 KB
Volume
52
Category
Article
ISSN
0040-4039

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✦ Synopsis


As part of an approach to the synthesis of the antitubercular agent elisapterosin B, we prepared two different chiral, non-racemic olefinic substrates and examined their diastereoselective ring closure using mercury salts. The effort yielded potential precursors to elisapterosin B in good yield with good to excellent diastereocontrol.


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