Asymmetric Michael-Type Additions of Lithium Amides to Aromatic Systems Leading to Novel. beta.-Amino Acids
M Shimano, AI Meyers
Index: Shimano, Masanao; Meyers Journal of the American Chemical Society, 1994 , vol. 116, # 14 p. 6437 - 6438
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Citation Number: 36
Abstract
There are numerous methods to introduce an amino group into an aromatic ring system that retain the aromaticity of the nucleus (path On the other hand, there appear to be no reported processes that directly introduce an amino group by interrupting the aromatic system, resulting in alicyclic amines (path B).
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