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Synfacts 2011(6): 0589-0589
DOI: 10.1055/s-0030-1259887
DOI: 10.1055/s-0030-1259887
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of ABT-341
H. Ishikawa, M. Honma, Y. Hayashi*
Tokyo University of Science, Japan
Further Information
Publication History
Publication Date:
19 May 2011 (online)

Significance
ABT-346 inhibits dipeptidyl peptidase IV, a serine protease that deactivates glucose-regulating hormones. It is currently a lead for the treatment of type-2 diabetes. The key step in this remarkably short synthesis of ABT-346 is an asymmetric Michael addition of acetaldehyde to the nitroalkene A catalyzed by the (R)-diphenylprolinol derivative B. Owing to the high efficiency and chemoselectivity of the component reactions, the six-step synthesis could be performed in a single pot in 63% overall yield without isolation of any intermediates.