## Abstract magnified image 2,6‐Bis(1__H__‐indole‐6‐yl)‐4__H__‐pyran‐4‐one **4** was synthesized __via__ Leimgruber–Batcho methodology starting from 2,6‐bis(4‐methyl‐3‐nitrophenyl)‐4__H__‐pyran‐4‐one **2**. Enamine intermediate in this reaction, **3**, reacts with aroyl chlorides in the presence o
✦ LIBER ✦
The Syntheses of 3-Substituted 4-(Pyridin-2-ylthio)indoles via Leimgruber—Batcho Indole Synthesis.
✍ Scribed by Ekaruth Srisook; Dae Yoon Chi
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 25 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
For Abstract see ChemInform Abstract in Full Text.
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