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- Challenges and potential for improving the druggability of podophyllotoxin-derived drugs in cancer chemotherapy. Wei Zhao, Ying Cong, Hong-Mei Li, Shengying Li, Yuemao Shen, Qingsheng Qi, Youming Zhang, Yue-Zhong Li, Ya-Jie Tang
, Nat. Prod. Rep.
, 2021
, 38
, 470
- XV.—A chemical investigation of the constituents of Indian and American Podophyllum (Podophyllum emodi and Podophyllum peltatum). Wyndham R. Dunstan, T. A. Henry
, J. Chem. Soc., Trans.
, 1898
, 73
, 209
- Silenes in organic synthesis: a concise synthesis of (±)-epi-picropodophyllin. Robert D. C. Pullin, Jonathan D. Sellars, Patrick G. Steel
, Org. Biomol. Chem.
, 2007
, 5
, 3201
- Lignans and related phenols. Part XII. Application of nuclear magnetic double resonance to the aryltetrahydronaphthalene class. D. C. Ayres, J. A. Harris, P. N. Jenkins, L. Phillips
, J. Chem. Soc., Perkin Trans. 1
, 1972
, 1343
- Biosynthesis, total synthesis, and pharmacological activities of aryltetralin-type lignan podophyllotoxin and its derivatives. Siyu Shen, Yuru Tong, Yunfeng Luo, Luqi Huang, Wei Gao
, Nat. Prod. Rep.
, 2022
, 39
, 1856
- Recent strategies and tactics for the enantioselective total syntheses of cyclolignan natural products. Rebekah G. Reynolds, Huong Quynh Anh Nguyen, Jordan C. T. Reddel, Regan J. Thomson
, Nat. Prod. Rep.
, 2022
, 39
, 670
- 28. Podophyllotoxin. Alexander Robertson, Roy B. Waters
, J. Chem. Soc.
, 1933
, 83
- A concise stereocontrolled formal total synthesis of (±)-podophyllotoxin using sulfoxide chemistry. Mike Casey, Claire M. Keaveney
, Chem. Commun.
, 2004
, 184
- Applications of Friedel–Crafts reactions in total synthesis of natural products. Majid M. Heravi, Vahideh Zadsirjan, Pegah Saedi, Tayebeh Momeni
, RSC Adv.
, 2018
, 8
, 40061
- 973. Lignans. Part II. Reduction of lactones of the podophyllotoxin group with lithium aluminium hydride. D. C. Ayres, P. J. S. Pauwels
, J. Chem. Soc.
, 1962
, 5025