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
AUTHORS (2)
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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