Abstract
A formal synthesis of a hepatitis C virus (HCV) inhibitor is described. The synthesis features a benzyne-mediated one-pot indoline formation-methylation sequence and an In(OTf)3-mediated mild oxa-Pictet-Spengler reaction for the synthesis of substituted electron-rich pyranoindole.
Original language | English |
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Article number | ST-2013-U0562-L |
Pages (from-to) | 2143-2147 |
Number of pages | 5 |
Journal | Synlett |
Volume | 24 |
Issue number | 16 |
DOIs | |
Publication status | Published - 2013 Aug 28 |
Keywords
- benzyne
- magnesium
- one-pot
- tandem reaction
- total synthesis
ASJC Scopus subject areas
- Organic Chemistry