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Asymmetric synthesis of ageliferin.


ABSTRACT: We describe herein an asymmetric synthesis of ageliferin. A Mn(III)-mediated oxidative radical cyclization reaction was used as the key step to construct the core skeleton of this pyrrole-imidazole dimer. This approach resembles the biogenic [4 + 2] dimerization in an intramolecular fashion.

SUBMITTER: Wang X 

PROVIDER: S-EPMC3183238 | biostudies-literature | 2011 Oct

REPOSITORIES: biostudies-literature

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Asymmetric synthesis of ageliferin.

Wang Xiao X   Ma Zhiqiang Z   Lu Jianming J   Tan Xianghui X   Chen Chuo C  

Journal of the American Chemical Society 20110908 39


We describe herein an asymmetric synthesis of ageliferin. A Mn(III)-mediated oxidative radical cyclization reaction was used as the key step to construct the core skeleton of this pyrrole-imidazole dimer. This approach resembles the biogenic [4 + 2] dimerization in an intramolecular fashion. ...[more]

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