Zhao F, Wang S J, Lin S, et al. Natural and unnatural anthraquinones isolated from the ethanol extract of the roots of Knoxia valerianoides[J]. Acta Pharm Sin B, 2012,2(3):260.
[5]
Lin C N, Chung M I, Gan K H, et al. Xanthones from formosan Gentianaceous plants[J]. Phytochemistry,1987, 26(8): 2381.
[6]
Zhang Z, Koike K, Jia Z, et al. Triterpenoidal saponins acylated with two monoterpenic acids from Gleditsia sinensis[J]. Chem Pharm Bull,1999, 47(3): 388.
[7]
赵卫权,丁立生,王明奎.木莓根部化学成分研究[J].中草药,2001,32(10): 874.
[8]
Kakuno T, Yoshikawa K, Arihara S. Triterpene saponins from fruit of Ilex crenata[J]. Phytochemistry,1992, 31(8): 2809.
[9]
Zhao Q S, Tian J, Yue J M, et al. Diterpenoids from Isodon flavidus[J]. Phytochemistry,1998, 48(6): 1025.
[10]
Nakatani M, Miyazaki Y, Iwashita T, et al. Triterpenes from Ilex rotunda fruits[J]. Phytochemistry,1989, 28(5): 1479.
[11]
Numata A, Yang P, Takahashi C, et al. Cytotoxic triterpenes from a Chinese medicine, Goreishi[J]. Chem Pharm Bull,1989, 37(3): 648.
[12]
Sousa M P, Matos M E O, Mmachado I L, et al. Triterpenoids from Guettarda angelica[J]. Phytochemistry,1984, 23(11): 2589.
[13]
Nandy a K, Podder G, Sahu N P, et al. Triterpenoids and their glucosides from Terminalia bellerica.[J]. Phytochemistry,1989, 28(10): 2769.
[14]
Seto T, Tanaka T, Tagahara O, et al. β-glucoside esters of 19α-hydroxyursolic acid derivatives in leaves of Rubus species[J]. Phytochemistry,1984, 23(12): 2829.
[15]
Barrero a F, Sanchez J F, Alvarez-Manzaneda E J, et al. Terpenoids and sterols from the wood of Abies pinsapo [J]. Phytochemistry,1993, 32(5): 1261.
[16]
Onocha P A, Okorie D, Connolly J D, et al. Monoterpene diol, iridoid glucoside and dibenzo-α-pyrone from Anthocleista djalonensis[J]. Phytochemistry,1995, 40(4): 1183.
[17]
Jones S R, Selinsky B S. Efficient route to 7α-(benzoyloxy)-3-dioxolane cholestan-24-(R)-ol, a key intermediate in the synthesis of squalamine[J]. J Org Chem,1998, 63: 3786.
[18]
Pettit G R, Numata A, Cragg G M, et al. Isolation and structures of schleicherastatins 1-7 and schleicheols 1 and 2 from the teak forest medicinal tree Schleichera oleosa[J]. J Nat Prod,2000, 63(1): 72.
[19]
Miyazawa M, Kasahara H, Kameoka H. Biotransformation of lignans: a specific microbial oxidation of(+)-eudesmin and(+)-magnolin by Aspergillus niger[J]. Phytochemistry,1993, 34(6): 1501.
Zeither K, Rose C A. An efficient carbene-catalyzed access to 3,4-dihydrocoumarins[J]. J Org Chem,2009, 74(4): 1759.
[26]
Mo S Y, Wang S J, Yang Y C, et al. Phelligridins C-F: cytotoxic pyrano [2] benzopyran-1,6-dione and furo pyran-4-one derivatives from the fungus Phellinus igniarius[J]. J Nat Prod, 2004, 67(5): 823.
[27]
Yoon J S, Lee M K, Sung S H, et al. Neuroprotective 2-(2-phenylethyl) chromones of Imperata cylindrica[J]. J Nat Prod, 2006, 69(2): 290.
[28]
Gan M L, Zhang Y L, Lin S, et al. Glycosides from the root of Iodes cirrhosa[J]. J Nat Prod, 2008, 71(4): 647.
Sacco R E, Waters W R, Rudolph K M, et al. Comparative nitric oxide production by LPS-stimulated monocyte-derived macrophages from Ovis canadensis and Ovis aries[J]. Comp Immunol Microbiol Infect Dis, 2006, 29(1):1.