Article ID Journal Published Year Pages File Type
5276007 Tetrahedron Letters 2012 4 Pages PDF
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
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