Total synthesis and biological evaluation of Wewakazole

Bohua Long , Jingzhao Zhang , Xueyan Wang , Xudong Tang , Zhengzhi Wu

Chemical Research in Chinese Universities ›› 2017, Vol. 33 ›› Issue (6) : 890 -894.

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Chemical Research in Chinese Universities ›› 2017, Vol. 33 ›› Issue (6) : 890 -894. DOI: 10.1007/s40242-017-7129-3
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Total synthesis and biological evaluation of Wewakazole

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Abstract

The total synthesis of Wewakazole was achieved on a gram scale, unambiguously confirming its structure. Three different substituted oxazoles present in this natural product were prepared efficiently. Biological evaluation indicated that Wewakazole significantly inhibited cancer cell proliferation in a dose-dependent manner.

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Wewakazole / Total synthesis / Biological evaluation

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Bohua Long, Jingzhao Zhang, Xueyan Wang, Xudong Tang, Zhengzhi Wu. Total synthesis and biological evaluation of Wewakazole. Chemical Research in Chinese Universities, 2017, 33(6): 890-894 DOI:10.1007/s40242-017-7129-3

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References

[1]

Davidson B. S. Chem. Rev., 1993, 93: 1771.

[2]

Gribble G. W. Mar. Drugs, 2015, 13: 4044.

[3]

Wang B. G., Gloer J. B., Ji N. Y., Zhao J. C. Chem. Rev., 2013, 113: 3632.

[4]

Gribble G. W. Heterocycles, 2012, 84: 157.

[5]

Gribble G. W. Acc. Chem. Res., 1998, 31: 141.

[6]

Zhao C., Zhu T., Zhu W. Chin. J. Org. Chem., 2013, 33: 1195.

[7]

Hu G. P., Yuan J., Sun L., She Z. G., Wu J. H., Lan X. J., Zhu X., Lin Y. C., Chen S. P. Mar. Drugs, 2011, 9: 514.

[8]

Blunt J. W., Copp B. R., Hu W. P., Munro M. H. G., Northcote P. T., Prinsep M. R. Nat. Prod. Rep., 2009, 26: 170.

[9]

Blunt J. W., Copp B. R., Munro M. H., Northcote P. T., Prinsep M. R. Nat. Prod. Rep., 2010, 27: 165.

[10]

Blunt J. W., Copp B. R., Munro M. H., Northcote P. T., Prinsep M. R. Nat. Prod. Rep., 2011, 28: 196.

[11]

Nestor J. J. Jr Curr. Med. Chem., 2009, 16: 4399.

[12]

Newman D. J., Gragg G. M. J. Nat. Prod., 2007, 70: 461.

[13]

Nogle L. M., Marquez B. L., Gerwick W. H. Org. Lett., 2003, 5: 3.

[14]

Long B., Tang S., Chen L., Qu S., Chen B., Liu J., Maguire A. R., Wang Z., Liu Y., Zhang H., Xu Z., Ye T. Chem. Commun., 2013, 49: 2977.

[15]

Long B., Zhang J., Tang X., Wu Z. Org. Biomol. Chem., 2016, 14: 9712.

[16]

Valdomir G., Padrónb J. I., Padrónc J. M., Martínc V. S., Davyt D. Synthesis, 2014, 46: 2451.

[17]

Moni L., Banfi L., Basso A., Carcone L., Rasparini M., Riva R. J. Org. Chem., 2015, 80: 3411.

[18]

Davies J. R., Kane P. D., Moody C. J. J. Org. Chem., 2005, 70: 7305.

[19]

Bertram A., Maulucci N., New O. M., Nora S. M. M., Pattenden G. Org. Biomol. Chem., 2007, 5: 1541.

[20]

Ferreira P. M. T., Castanheira E. M. S., Monteiro L. S., Pereira G., Vilaça H. Tetrahedron, 2010, 66: 8672.

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