✦ LIBER ✦

ChemInform Abstract: Sequential Sonogashira/Carbopalladative Cyclization/Suzuki Reactions Catalyzed by a Single Palladium Source by Using Protected Homopropargyl Alcohol.

✍ Scribed by Xin Wang; Lingyan Liu; Weixing Chang; Jing Li

Publisher: John Wiley and Sons
Year: 2011
Weight: 41 KB
Volume: 42
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201107125

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

Protected homopropargyl alcohol (I) is converted into indene derivatives by a new cascade sequence including Sonogashira coupling with aryl iodides (II) or aryl bromides (V), carbopalladative cyclization and Suzuki coupling with aryl boronic acids (III).

📜 SIMILAR VOLUMES

Sequential Sonogashira/Carbopalladative

Sequential Sonogashira/Carbopalladative Cyclization/Suzuki Reactions Catalyzed by a Single Palladium Source by Using Protected Homopropargyl Alcohol

✍ Xin Wang; Lingyan Liu; Weixing Chang; Jing Li 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 157 KB

## Abstract A novel cascade combination reaction catalyzed by a single palladium source for the synthesis of various indene derivatives is reported. The approach involved sequential Sonogashira/carbopalladative cyclization/Suzuki coupling reactions by using three readily available components, such