Abstract
A facile technique involving a novel Lewis-acid-catalyzed tandem selective ring-opening of oxirane and Friedel-Crafts alkylation of 1H-indol-1-yl derived oxiranes was developed. The developed protocol affords functionalized [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines in up to 95% yield. This journal is
| Original language | English |
|---|---|
| Pages (from-to) | 6869-6877 |
| Number of pages | 9 |
| Journal | Organic and Biomolecular Chemistry |
| Volume | 12 |
| Issue number | 35 |
| DOIs | |
| State | Published - 21 Sep 2014 |
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Dive into the research topics of 'Scandium-catalyzed tandem selective oxirane ring-opening/Friedel-Crafts alkylation: A facile access to [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines'. Together they form a unique fingerprint.Cite this
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