Four neolignan ketones fromPiper capense
作者： Terrence P. Green , David F. Wiemer
DOI: 10.1016/0031-9422(91)80104-9
关键词:
摘要: Abstract Further studies of a chloroform extract ofPiper capense roots have resulted in the isolation and characterization four new neolignans. Three these compounds are unusual 2′-oxo-8.1′-neolignans, while fourth is more common 6′-oxo-8.3′-neolignan variety.
elsevier.com
sci-hub.se 参考文章(8)
Vassilios Roussis, Steph̀en A. Ampofo, David F. Wiemer, A prenylated benzoic acid derivative from the leaves of Piper taboganum Phytochemistry. ,vol. 29, pp. 1787- 1788 ,(1990) , 10.1016/0031-9422(90)85016-9
Ad Bax, Structure determination and spectral assignment by pulsed polarization transfer via long-range 1H13C couplings Journal of Magnetic Resonance (1969). ,vol. 57, pp. 314- 318 ,(1984) , 10.1016/0022-2364(84)90133-1
Gerald B. Hammond, Norman C. Baenziger, David F. Wiemer, Dammara-20,25-dien-3β,24α-diol: A natural repellent of Acromyrmex octospinosus Phytochemistry. ,vol. 29, pp. 783- 785 ,(1990) , 10.1016/0031-9422(90)80018-C
Stephen A. Ampofo, Vassilios Roussis, David F. Wiemer, New prenylated phenolics from Piper auritum Phytochemistry. ,vol. 26, pp. 2367- 2370 ,(1987) , 10.1016/S0031-9422(00)84721-4
Terrence P. Green, Deborah L. Galinis, David F. Wiemer, Three neolignans from the roots of Piper capense Phytochemistry. ,vol. 30, pp. 1649- 1652 ,(1991) , 10.1016/0031-9422(91)84226-I
Yoshikazu Shizuri, Kensuke Nakamura, Shosuke Yamamura, Shigeru Ohba, Hiroshi Yamashita, Yoshihiko Saito, Total syntheses of isodihydrofutoquinol a, futoquinol, and isofutoquinol A and B Tetrahedron Letters. ,vol. 27, pp. 727- 730 ,(1986) , 10.1016/S0040-4039(00)84085-X
D. A. Whiting, Ligans and neolignans Natural Product Reports. ,vol. 2, pp. 191- 211 ,(1985) , 10.1039/NP9850200191
Kuniaki Matsui, Katsura Munakata, Four new neolignans from piper futokadzura Tetrahedron Letters. ,vol. 17, pp. 4371- 4374 ,(1976) , 10.1016/0040-4039(76)80118-9