Enantioselective Total Synthesis of (−)‐Lansai B and (+)‐Nocardioazines A and B

heterocycles Biological Products Cycloaddition Reaction Molecular Structure natural products Stereoisomerism 540 01 natural sciences 0104 chemical sciences 3. Good health macrocycles Acids, Heterocyclic total synthesis cycloaddition
DOI: 10.1002/ange.201402571 Publication Date: 2014-04-28T13:27:06Z
ABSTRACT
Abstract The concise total syntheses of the bis(pyrroloindolines) (−)‐lansai B and (+)‐ nocardioazines A are reported. key pyrroloindoline building blocks rapidly prepared by enantioselective formal [3+2] cycloaddition reactions. macrocycle (+)‐nocardioazine is constructed an unusual intramolecular diketopiperazine formation.
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