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A Facile and Efficient Synthesis of Caeliferin a 16:0

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Chemistry of Natural Compounds Aims and scope

The simplest and efficient route to synthesis of caeliferin A 16:0 (1) has been developed via bromination of 16-hexadecanolide (2) and sulfonation of 2,16-dihydroxyhexadecanoic acid in two steps in an overall 82% yield.

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Acknowledgment

This work was supported financially by the Fundamental Research Funds for the Central Universities (Grant No. 31920130062).

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Authors and Affiliations

  1. Institute of Chemical Engineering, Northwest University for Nationalities, 730030, Lanzhou, P. R. China

    Cheng Peng

  2. School of Chemical Biology and Biotechnology, Peking University Shenzhen Graduate School, 518055, Shenzhen, P. R. China

    Dong-Peng He & Shuo Li

  3. School of Life Science and Engineering, Lanzhou University of Technology, 730050, Lanzhou, P. R. China

    Zhong-Duo Yang

Authors
  1. Cheng Peng
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  2. Dong-Peng He
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  3. Shuo Li
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  4. Zhong-Duo Yang
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Corresponding authors

Correspondence to Cheng Peng or Shuo Li.

Additional information

Published in Khimiya Prirodnykh Soedinenii, No. 2, March–April, 2016, pp. 175–176.

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Peng, C., He, DP., Li, S. et al. A Facile and Efficient Synthesis of Caeliferin a 16:0. Chem Nat Compd 52, 199–201 (2016). https://doi.org/10.1007/s10600-016-1593-8

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  • DOI: https://doi.org/10.1007/s10600-016-1593-8

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