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
Link To Document :
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