Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 9, Issue 21, Pages 7351-7357Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1ob05936j
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Funding
- National Science Foundation of China [20872079]
- Natural Science Foundation of Shandong Province [2009ZRB019YA]
- State Key Laboratory of Natural and Biomimetic Drugs of Peking University [K20090205]
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A transition metal-free process for the regioselective synthesis of pyrrolo[1,2-a]quinoxalines under mild conditions in one-pot is described. The reaction afforded a variety of products in good to excellent yields. Indolo[1,2-a] quinoxalines were also synthesized from indole-2-carboxamides under the same conditions.
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