- 1) Wani, M. C., Taylor, H. L., Wall, M. E., Coggon, P., and Mcphail, A. T., Plant antitumor agents. IV. The isolation and structure of taxol, a novel antileukemic and antitumor agent from Taxus brevifolia. J. Am. Chem. Soc., 93, 2325-2327 (1971).
- . 1995. p. 31- 57.
- . 1993. p. 1- 206.
- 4) Appendino, G., The phytochemistry of the yew tree. Nat. Prod. Rep., 12, 349-360 (1995).
- 5) Sugiyama, T., Oritani, T., and Oritani, T., A novel taxane diterpenoid from Japanese yew, Taxus cuspidata. Biosci. Biotechnol. Biochem., 58, 1923-1924 (1994).
- 6) Shi, Q.-W., Oritani, T., Sugiyama, T., and Kiyota, H., Two new taxanes from Taxus chinensis var. mairei. Planta Medica, 64, 766-769 (1998).
- 7) Shi, Q.-W., Oritani, T., Horiguchi, T., Sugiyama, T., Murakami, R., and Yamada, T., Four novel taxane diterpenoids from the needles of Japanese yew, Taxus cuspidata. Biosci. Biotechnol. Biochem., 63, 924-929 (1999).
- 8) Shi, Q.-W., Oritani, T., Sugiyama, T., Murakami, R., and Wei, H.-Q., Six new taxane diterpenoids from the seeds of Taxus chinensis var. mairei and Taxus yunnanensis. J. Nat. Prod., 62, 1114-1118 (1999).
- 9) Murakami, R., Shi, Q.-W., Oritani, T., Horiguchi, T., and Oritani, T., A novel rearranged taxoid from the needles of Japanese yew, Taxus cuspidata Sieb. et Zucc. Biosci. Biotechnol. Biochem., 63, 1660-1663 (1999).
- 10) Shi, Q.-W., Oritani, T., Sugiyama, T., Horiguchi, T., and Kiyota, H., Three new rearranged taxane diterpenoids from the bark of Taxus chinensis var. mairei and the needles of Taxus cuspidata. Heterocycles, 51, 841-850 (1999).
- 11) Shi, Q.-W., Oritani, T., Sugiyama, and Cheng, Q., Three novel bicyclic taxoids from the needles of the Chinensis yew, Taxus chinensis var. mairei. Chin. Chem. Lett., 10, 481-484 (1999).
- 12) Shi, Q.-W., Oritani, T., Sugiyama, T., Horiguchi, T., Murakami, R., Zhao, D., and Oritani, T., Three new taxane diterpenoids from the seeds of Taxus yunnanensis Cheng et L. K. Fu and T. cuspidata Sieb et Zucc. Tetrahedron, 55, 8365-8376 (1999).
- 13) Cheng, Q., Oritani, T., and Horiguchi, T., (iPrO)3TiCl-induced reactions of α- and β-4(20)-epoxy-5-hydroxytriacetyltaxicin-I. Tetrahedron, 55, 12099-12108 (1999).
- 14) Cheng, Q., Oritani, T., and Horiguchi, T., Et2AlCl-mediated reaction of α-4(20)-epoxy-5-hydroxy Taxinine B. Chin. Chem. Lett., in press (1999).
- 15) Appendino, G., Lusso, P., Gariboldi, P., Bombardelli, E., and Gabetta, B., A 3,11-cyclotaxane from Taxus baccata. Phytochemistry, 31, 4259-4262 (1992).
- 16) Woods, M. C., Chiang, H.-C., Nakadaira, Y., and Nakanishi, K., The nuclear overhauser effect, a unique method of defining the relative stereochemistry and conformation of taxane derivatives. J. Am. Chem. Soc., 90, 522-523 (1968).
- 17) Yoshizaki, F., Madarame, M., Takahashi, C., and Hisamichi, S., Principal constituents of the seeds of Japanese yew (Taxus cuspidata). Shoyakugaku Zashi (in Japanese), 40, 429-433 (1986).
Full access
Two Novel Taxane Diterpenoids From the Needles of Japanese Yew, Taxus Cuspidata
Reprints and Corporate Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
To request a reprint or corporate permissions for this article, please click on the relevant link below:
Academic Permissions
Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?
Obtain permissions instantly via Rightslink by clicking on the button below:
If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.
Related research
People also read lists articles that other readers of this article have read.
Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.
Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.