[1]
R. C. Cambie, R. A. Franich, D. Larsen, et al., Potential ambergris odorants from abietic acid, Australian Journal of Chemistry. 43(1990)21-46.
DOI: 10.1071/ch9900021
Google Scholar
[2]
M. C. Costa, S. P. Alves, M. E. Correia, et al., Synthesis of an ambergris-type ketal from abietic acid, Synthesis. 2006(2006)1171-1175.
DOI: 10.1055/s-2006-926392
Google Scholar
[3]
J. S. Yadav, G. Baishya, U. Dash, Synthesis of (+) -amberketal and its analog from l-abietic acid, Tetrahedron. 63(2007) 9896-9902.
DOI: 10.1016/j.tet.2007.06.063
Google Scholar
[4]
A. Presser, I. Pötschger, E. Haslinger, et al., Synthetic transformations of abietic acid Vа: Structure modification and ozonization, Monatshefte fur Chemie. 133(2002)231-239.
DOI: 10.1007/s007060200000
Google Scholar
[5]
B. Gigante, C. Santos, A. M. Silva, et al., Catechols from abietic acid: synthesis and evaluation as bioactive compounds, Bioorganic & Medicinal Chemistry. 11(2003) 1631-1638.
DOI: 10.1016/s0968-0896(03)00063-4
Google Scholar
[6]
M. A. González, J. Correa-Royero, L. Agudelo, et al., Synthesis and biological evaluation of abietic acid derivatives, European Journal of Medicinal Chemistry. 44(2009)2468-2472.
DOI: 10.1016/j.ejmech.2009.01.014
Google Scholar
[7]
C. H. Lin, H. S. Chuang, Use of abietic acid and derivatives thereof for inhibiting cancer, U. S. Patent 7, 015, 248B2. (2006).
Google Scholar
[8]
M. A. Fernández, M. P. Tornos, M. D. García, et al., Anti-inflammatory activity of abietic acid, a diterpene isolated from pimenta racemosa var. grissea, Journal of Pharmacy and Pharmacology. 53(2001)867-872.
DOI: 10.1211/0022357011776027
Google Scholar
[9]
T. Nobuyuki, K. Teruo, G. Tsuyoshi, et al., Abietic acid activates peroxisome proliferator-activated receptor-γ( PPARγ) in RAW264. 7 macrophages and 3T3-L1 adipocytes to regulate gene expression involved in inflammation and lipid metabolism, Federation of European Biochemical Societies Letters. 550(2003).
DOI: 10.1016/s0014-5793(03)00859-7
Google Scholar
[10]
E. Alvarez-Manzaneda, R. Chahboun, F. Bentaleb, et al., Regioselective routes towards 14-hydroxyabietane diterpenes. A formal synthesis of immunosuppressant (-)-triptolide from (+)-abietic acid, Tetrahedron. 63(2007)11204-11212.
DOI: 10.1016/j.tet.2007.07.088
Google Scholar
[11]
M. Hiroshi, O. Katsuya, E. Hiroshi, et al., Abietamide derivatives, their production and use, U. S. Patent 4, 210, 671(A). (1980).
Google Scholar
[12]
L. Y. Zheng, S. W. Zhang, L. Zheng, et al., Sulphonated dehydrogenated sylvate, the preparation and use, U. S. Patent 20, 040, 162, 341(A1). (2004).
Google Scholar
[13]
N. N. Ulusu, D. Ercil, M. Sakar, et al., Abietic acid inhibits lipoxygenase activity, Phytotherapy Research. 16(2002) 88-90.
DOI: 10.1002/ptr.983
Google Scholar
[14]
Y. Aya, E. Yoichiro, M. Kohtaro, et al., Supercritical fluid chromatography of free resin acids on an ODS-silica gel column, Journal of Chromatography A. 709(1995)345-349.
DOI: 10.1016/0021-9673(95)00442-p
Google Scholar
[15]
S. Sadhra, C. N. Gray, I. S. Foulds, High-performance liquid chromatography of unmodifed rosin and its applications in contact dermatology, Journal Of Chromatography B. 700(1997)101-110.
DOI: 10.1016/s0378-4347(97)00293-4
Google Scholar
[16]
A. Findeisen, V. Kolivoska, I. Kaml, et al., Analysis of diterpenoic compounds in natural resins applied as binders in museum objects by capillary electrophoresis, Journal of Chromatography A. 1157(2007)454-461.
DOI: 10.1016/j.chroma.2007.05.010
Google Scholar
[17]
J. K. He, Q. J. Li, Comprehensive Treatise on Torest Chemical Industry, Beijing, China Forestry Press, (2001).
Google Scholar
[18]
G. C. Harris, T. F. Sanderson, Resin acids. I. An improved method of isolation of resin acids; the isolation of a new abietic-type acid, neoabietic acid, Journal American Chemical Society. 70(1948)334-339.
DOI: 10.1021/ja01181a104
Google Scholar
[19]
Y. He, Y. M. Zhang, J. Lu, et al., Isolation and structural elucidation of abietic acid as the main adulterant in an herbal drug for the treatment of psoriasis, Journal of Pharmaceutical and Biomedical Analysis. 66(2012)345-348.
DOI: 10.1016/j.jpba.2012.03.007
Google Scholar