Title of article
Total synthesis of (±)-martinelline
Author/Authors
Xia، نويسنده , , Chengfeng and Heng، نويسنده , , Linshen and Ma، نويسنده , , Dawei، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
5
From page
9405
To page
9409
Abstract
The squaric acid-catalyzed imino-Diels–Alder reaction of enamine 4 with the imine 5 provides the pyrroloquinolines 6 and 7, which were converted to the triamine 3 using regioselective reduction and a Wittig reaction as the key steps. Guanylation of 3 followed by coupling with the alcohol 19 furnished the total synthesis of (±)-martinelline.
Journal title
Tetrahedron Letters
Serial Year
2002
Journal title
Tetrahedron Letters
Record number
1659631
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