Bioinspired total synthesis of katsumadain A by organocatalytic enantioselective 1,4-conjugate addition

Yongguang Wang, Ruiyang Bao, Shengdian Huang and Yefeng Tang
Beilstein J. Org. Chem. 2013, 9, 1601–1606. https://doi.org/10.3762/bjoc.9.182

Supporting Information

Supporting Information File 1: Experimental procedures and characterization data for synthetic 1, 3ac, 5ak and 9ak.
Format: PDF Size: 5.2 MB Download

Cite the Following Article

Bioinspired total synthesis of katsumadain A by organocatalytic enantioselective 1,4-conjugate addition
Yongguang Wang, Ruiyang Bao, Shengdian Huang and Yefeng Tang
Beilstein J. Org. Chem. 2013, 9, 1601–1606. https://doi.org/10.3762/bjoc.9.182

How to Cite

Wang, Y.; Bao, R.; Huang, S.; Tang, Y. Beilstein J. Org. Chem. 2013, 9, 1601–1606. doi:10.3762/bjoc.9.182

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • Sarker, A.; Gu, Z.; Mao, L.; Ge, Y.; Hou, D.; Fang, J.; Wei, Z.; Wang, Z. Influenza-existing drugs and treatment prospects. European journal of medicinal chemistry 2022, 232, 114189. doi:10.1016/j.ejmech.2022.114189
  • Wang, N.; Wu, Z.; Wang, J.; Ullah, N.; Lu, Y. Recent applications of asymmetric organocatalytic annulation reactions in natural product synthesis. Chemical Society reviews 2021, 50, 9766–9793. doi:10.1039/d0cs01124j
  • Wang, Z. Advances in the Asymmetric Total Synthesis of Natural Products Using Chiral Secondary Amine Catalyzed Reactions of α,β-Unsaturated Aldehydes. Molecules (Basel, Switzerland) 2019, 24, 3412. doi:10.3390/molecules24183412
  • Reyes-Rodríguez, G. J.; Rezayee, N. M.; Vidal-Albalat, A.; Jørgensen, K. A. Prevalence of Diarylprolinol Silyl Ethers as Catalysts in Total Synthesis and Patents. Chemical reviews 2019, 119, 4221–4260. doi:10.1021/acs.chemrev.8b00583
  • Obydennov, D. L.; El-Tantawy, A. I.; Sosnovskikh, V. Y. Triacetic acid lactone as a bioprivileged molecule in organic synthesis. Mendeleev Communications 2019, 29, 1–10. doi:10.1016/j.mencom.2019.01.001
  • Feng, J.; Lei, X.; Guo, Z.; Tang, Y. Total Synthesis of Homodimericin A. Angewandte Chemie (International ed. in English) 2017, 56, 7895–7899. doi:10.1002/anie.201702893
  • Feng, J.; Lei, X.; Guo, Z.; Tang, Y. Total Synthesis of Homodimericin A. Angewandte Chemie 2017, 129, 8003–8007. doi:10.1002/ange.201702893
  • Dibello, E.; Gamenara, D.; Seoane, G.
Other Beilstein-Institut Open Science Activities