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Volume 4 |
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New N-protected Aminoaldehydes |
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The Squarix Newsletter provides you with information about our innovative building blocks, reactive intermediates and screening compounds from our Discovery Chemicals portfolio. |
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In this issue we present new N-protected Aminoaldehydes especially designed for stereocontrolled organic synthesis. |
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Featured Products |
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These compounds are derived from natural and unnatural amino acids and are not commercially available from other manufacturers. |
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See our website for the full line of building blocks or download the Discovery Chemicals catalogue. |
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Please find also some selected references from the literature describing interesting applications of N-protected aminoaldehydes. The (E)-alkene dipeptide isostere of Trp-Val was synthesized using the key building block AL044 (Noda et al.). Evans et al. reported an efficient syntheses of L-Statine using L-Leucinal (AL040) as starting material :
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References |
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M. Noda, T. Ibuka, H. Habashita, and N. Fuji, A Highly Stereoselective Synthesis of the Functionalized (E)-Alkene Dipeptide Isostere of Trp-Val via Organocyanocopper-Lewis Acid Mediated Reaction, Chem. Pharm. Bull 1997, 45, 1259-1264. |
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K.E. Rittle, C.F. Homnick, G.S. Ponticello and B.E. Evans, A Synthesis of Statine Utilizing an Oxidative Route to Chiral α-Amino Aldehydes1982, J. Org. Chem. 47, 3016-3018. |
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