Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5276007 | Tetrahedron Letters | 2012 | 4 Pages |
Abstract
The first concise total syntheses of pyrroloquinoline natural products, Marinoquinolines A-C, have been achieved in six linear steps from commercially available starting materials. The key steps were a reaction between (p-tolylsulfonyl)methylisocyanide (TosMIC) and α, β-unsaturated ester under basic condition to prepare the pyrrole moiety and Morgen-Walls reaction to construct quinoline ring.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Lijun Ni, Ziyuan Li, Fan Wu, Jinyi Xu, Xiaoming Wu, Lingyi Kong, Hequan Yao,