Title of article
Concise total syntheses of Marinoquinolines A–C
Author/Authors
Ni، نويسنده , , Lijun and Li، نويسنده , , Ziyuan and Wu، نويسنده , , Fan and Xu، نويسنده , , Jinyi and Wu، نويسنده , , Xiaoming and Kong، نويسنده , , Lingyi and Yao، نويسنده , , Hequan، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2012
Pages
4
From page
1271
To page
1274
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.
Keywords
natural product , Marinoquinoline , antitumor , total synthesis , Pyrroloquinoline
Journal title
Tetrahedron Letters
Serial Year
2012
Journal title
Tetrahedron Letters
Record number
1880240
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