Design, synthesis, and biological activity evaluation of (-)-6-O-desmethylantofine analogues as potent anti-cancer agents.

@article{Han2019DesignSA,
  title={Design, synthesis, and biological activity evaluation of (-)-6-O-desmethylantofine analogues as potent anti-cancer agents.},
  author={Guifang Han and Lihua Qing and Meng Wu and Yu-xiang Wang and Yuxiu Liu and Xue-ling Liu and Ziwen Wang and Jian Ding and Linghua Meng and Qingmin Wang},
  journal={Bioorganic \& medicinal chemistry},
  year={2019}
}
3 Citations
Total Synthesis of Indolizidine Alkaloids via Nickel-Catalyzed (4 + 2) Cyclization.
A Ni-catalyzed (4 + 2) cycloaddition of alkynes and azetidinones toward piperidinones was used as key reaction in the enantioselective synthesis of naturally occurring indolizidine alkaloids. The

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