| Autor: |
Jamison CR; Department of Chemistry, Princeton University, 192 Frick Laboratory, Princeton, New Jersey 08540, USA., Badillo JJ; Department of Chemistry, Princeton University, 192 Frick Laboratory, Princeton, New Jersey 08540, USA., Lipshultz JM; Department of Chemistry, Princeton University, 192 Frick Laboratory, Princeton, New Jersey 08540, USA., Comito RJ; Department of Chemistry, Princeton University, 192 Frick Laboratory, Princeton, New Jersey 08540, USA., MacMillan DWC; Department of Chemistry, Princeton University, 192 Frick Laboratory, Princeton, New Jersey 08540, USA. |
| Abstrakt: |
In nature, many organisms generate large families of natural product metabolites that have related molecular structures as a means to increase functional diversity and gain an evolutionary advantage against competing systems within the same environment. One pathway commonly employed by living systems to generate these large classes of structurally related families is oligomerization, wherein a series of enzymatically catalysed reactions is employed to generate secondary metabolites by iteratively appending monomers to a growing serial oligomer chain. The polypyrroloindolines are an interesting class of oligomeric natural products that consist of multiple cyclotryptamine subunits. Herein we describe an iterative application of asymmetric copper catalysis towards the synthesis of six distinct oligomeric polypyrroloindoline natural products: hodgkinsine, hodgkinsine B, idiospermuline, quadrigemine H and isopsychotridine B and C. Given the customizable nature of the small-molecule catalysts employed, we demonstrate that this strategy is further amenable to the construction of quadrigemine H-type alkaloids not isolated previously from natural sources. |
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