Literature DB >> 21919153

A synthetic study of atropurpuran: construction of a pentacyclic framework by an intramolecular reverse-electron-demand Diels-Alder reaction.

Takahiro Suzuki1, Aya Sasaki, Naoki Egashira, Susumu Kobayashi.   

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Year:  2011        PMID： 21919153     DOI： 10.1002/anie.201103950

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  4 in total

1.  A tandem 1,3-H-shift-6π-electrocyclization-cyclic 2-amido-diene intramolecular Diels-Alder cycloaddition approach to BCD-Ring of atropurpuran.

Authors:  Ryuji Hayashi; Zhi-Xiong Ma; Richard P Hsung
Journal:  Org Lett       Date:  2011-12-13       Impact factor: 6.005

Review 2.  Non-alkaloidal constituents from the genus Aconitum: a review.

Authors:  Tianpeng Yin; Hao Zhou; Le Cai; Zhongtao Ding
Journal:  RSC Adv       Date:  2019-04-02       Impact factor: 4.036

Review 3.  Retrosynthetic strategies and their impact on synthesis of arcutane natural products.

Authors:  Shelby V McCowen; Nicolle A Doering; Richmond Sarpong
Journal:  Chem Sci       Date:  2020-04-21       Impact factor: 9.825

4.  Total synthesis of atropurpuran.

Authors:  Jing Gong; Huan Chen; Xiao-Yu Liu; Zhi-Xiu Wang; Wei Nie; Yong Qin
Journal:  Nat Commun       Date:  2016-07-08       Impact factor: 14.919
  4 in total

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