5 research outputs found

    Di- and tripeptide segments of zervamicin II-2: Z-Thr(OBn)-Aib-N(Me)Ph and Z-Val-Aib-Hyp(OBn)-OMe

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    The title compounds, O-benzyl-N-(benzyl­oxy­carbonyl)­threonyl-2,N-dimethyl­alanin­anilide, C30H35N3O5, and methyl (4R)-4-benzyl­oxy-N-(benzyl­oxy­carbonyl)­valyl-2-(methyl­alanyl)prolinate, C30H39N3O7, were obtained from the `azirine coupling' of the corresponding protected amino acids with 2,2,N-trimethyl-2H-azirin-3-amine and methyl (4R)-4-(benzyl­oxy)-N-(2,2-dimethyl-2H-azirin-2-yl)prolinate, respectively. The Aib unit in each mol­ecule has the greatest turn- or helix-inducing effect on the mol­ecular conformation. Inter­molecular N—H⋯O inter­actions link the mol­ecules of the tripeptide into sheets and those of the dipeptide into extended chains

    Ligand-Accelerated C−H Activation Reactions: Evidence for a Switch of Mechanism

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