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Highly Enantioselective Lewis Base Organocatalyzed Hydrosilylation of γ-Imino Esters

✍ Scribed by Zhou-Yang Xue; Li-Xin Liu; Yan Jiang; Wei-Cheng Yuan; Xiao-Mei Zhang

Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
419 KB
Volume
2012
Category
Article
ISSN
1434-193X

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Highly Enantioselective Synthesis of β-A
Highly Enantioselective Synthesis of β-Amino Acid Derivatives by the Lewis Base Catalyzed Hydrosilylation of β-Enamino Esters
✍ Hong-Jie Zheng; Wen-Bing Chen; Zhi-Jun Wu; Jin-Gen Deng; Wen-Qing Lin; Wei-Cheng 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 249 KB 👁 1 views

Optically active b-amino acids are very important chiral building blocks for the synthesis of b-peptides, b-lactams, natural products, and physiologically active substances. [1] Therefore, efficient methods for the synthesis of optically active b-amino acids would be of great value for drug discover