Readily available α-amino aldehydes, incorporating a methylthiomethyl (MTM) protecting group on nitrogen, are shown to be efficient substrates in Rh-catalyzed alkyne hydroacylation reactions. The reactions are performed under mild conditions, employing a small-bite-angle bis-phosphine ligand, allowing for good functional group tolerance with high stereospecificity. Amino aldehydes derived from glycine, alanine, valine, leucine, phenylalanine, isoleucine, serine, tryptophan, methionine, and cysteine were successfully employed, as was an enantiomerically enriched α-OMTM-aldehyde derived from phenyllactic acid. The synthetic utility of the α-amino enone products is demonstrated in a short enantioselective synthesis of the natural product sphingosine.

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Kehrt, marsch! Ein von einer Aminosäure abgeleiteter Alkohol und ein Arylamid wurden zu einem Kehrenbaustein für Peptidkonformationen kombiniert. Cyclopropananaloga von Tetra‐ und Hexapeptiden bilden parallele Faltblattstrukturen, die durch CH⋅⋅⋅O‐Wasserstoffbrücken stabilisiert werden (siehe Schema). NMR‐spektroskopische Studien bestätigen das Vorliegen von Wasserstoffbrücken.