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Highly Enantioselective Michael Addition of Malononitrile to Vinylogous Imine Intermediates Generated in situ from Arylsulfonyl Indoles

✍ Scribed by Linhai Jing; Jiangtao Wei; Li Zhou; Zhiyong Huang; Zhengkai Li; Dr. Di Wu; Haifeng Xiang; Prof. Dr. Xiangge Zhou

Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
225 KB
Volume
16
Category
Article
ISSN
0947-6539

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ChemInform Abstract: Highly Enantioselec
ChemInform Abstract: Highly Enantioselective Michael Addition of Malononitrile to Vinylogous Imine Intermediates Generated in situ from Arylsulfonyl Indoles.
✍ Linhai Jing; Jiangtao Wei; Li Zhou; Zhiyong Huang; Zhengkai Li; Di Wu; Haifeng X 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 40 KB 👁 1 views

## Abstract The first highly enantioselective Michael addition of malononitrile to arylsulfonylindole‐derived vinylogous imine intermediates is presented.