Concise and Efficient Total Syntheses of Virenamides A and D

Authors

  • Gan Haifeng College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing 211816
  • Chen Zhengbang College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing 211816
  • Fang Zheng School of Pharmaceutical Sciences, Nanjing University of Technology, Nanjing 211816
  • Guo Kai College of Biotechnology and Pharmaceutical Engineering, Nanjing University of Technology, Nanjing 211816

DOI:

https://doi.org/10.24297/jac.v4i3.945

Keywords:

Total syntheses, Virenamide, Ascidian Diplosoma virens, Thiazole

Abstract

Concise total syntheses of linear thiazole-containing peptides virenamides A (1) and D (4), isolated from Australian ascidian Diplosoma virens have been accomplished from Boc-L-valine (6) in 7 steps. A cyclization between thioamide and bromoacetaldehyde was applied to form thiazole ring as a key step.

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Published

2008-12-12

How to Cite

Haifeng, G., Zhengbang, C., Zheng, F., & Kai, G. (2008). Concise and Efficient Total Syntheses of Virenamides A and D. JOURNAL OF ADVANCES IN CHEMISTRY, 4(3), 488–493. https://doi.org/10.24297/jac.v4i3.945

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Section

Articles