Thursday, 17 May 2007
3rd Floor Hall (Pfahler Hall)
366

Asymmetric synthesis of syn-(2R, 3S)-diaminopropanoates from sulfinimines (N-sulfinyl imines)

Franklin A. Davis, Yanfeng Zhang, Jianghe Deng, and Danyang Li. Temple University, Philadelphia, PA

a,b-Diamino acids are important structural fragments of biologically active compounds. syn-(2R,3S)-Diaminopropanoates were readily prepared by adding the prochiral lithium enolate of ethyl (dibenzylamino)acetate to various sulfinimines (N-sulfinyl imines). To demonstrate the efficiency of this new methodology, the formal synthsis of (+)-CP-99,994 and (+)-CP-122,721 will be presented.


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