期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 133, 期 4, 页码 740-743出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja110117g
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资金
- NIH [GM083428]
- American Chemical Society
- Barry M. Goldwater Foundation
A robust route to 2,4-disubstituted pyrrole heterocycles relying upon a cascade reaction is reported. The reaction benefits from operational simplicity: it is air and moisture tolerant and is performed at ambient temperature. Control over the reaction conditions provides ready access to isopyrroles, 2,3,4-trisubstituted pyrroles, and 3-substituted pyrollidin-2-ones.
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