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21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2
214.16,182.02,144.45,128.06,62.54,60.46,54.05,48.19,43.91,43.35,42.78,40.41,39.30,38.81,37.61,28.39,24.24,18.86,18.17,15.43,14.82
ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ
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1 . ent-18-acetoxykaur-15-en-7-one
C22H32O3 ÏàËƶÈ:63.6%
Journal of Natural Products 1990 Vol 53 441
Microbial Transformation of Tetracyclic Diterpenes: Conversion of ent-Kaurenones by Curvularia and Rhizopus Strains
Andres Garcia-Granados, Antonio Martinez, Antonio Ortiz, Maria Esther Onorato, Jose Maria Arias
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
2 . ent-18-hydroxykaur-15-en-7-one
ÏàËƶÈ:61.9%
Journal of Natural Products 1990 Vol 53 441
Microbial Transformation of Tetracyclic Diterpenes: Conversion of ent-Kaurenones by Curvularia and Rhizopus Strains
Andres Garcia-Granados, Antonio Martinez, Antonio Ortiz, Maria Esther Onorato, Jose Maria Arias
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
3 . siderone
C20H28O3 ÏàËƶÈ:61.9%
Phytochemistry 1983 22 2537-2538
Siderone, a diterpene from Sideritis syriaca
Pietro Venturella, Aurora Bellino, Maria Luisa Marino
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
4 . 3¦Â-hydroxy-12-en-ursolic acid
ÏàËƶÈ:59.0%
Acta Bot. Boreal. -Occident. Sin. 2005 25 1234-1237
Lipid-soluble Chemical Constituents in Sonchus oleraceus
HU Pei-zhuo, ZOU Chuan-zong, ZHU Ying
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
5 . euphoranginol A 11-acetate
C22H34O3 ÏàËƶÈ:59.0%
Journal of Natural Products 1994 Vol 57 811
ent-Kaurane Diterpenoids from Euphorbia wangii
Zhong-Jian Jia, Jian-Gong Shi, Li Yang
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
6 . andrographic acid
C20H28O6 ÏàËƶÈ:57.1%
Chemical & Pharmaceutical Bulletin 2007 55(3) 455-458
Secondary Metabolites from Andrographis paniculata
Wenkui LI,Xudong XU,Hongjie ZHANG,Cuiying MA,Harry FONG,Richard VAN BREEMEN,and John FITZLOFF
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
7 . 15-normanoyloxide-14,18-dioic acid
C19H30O5 ÏàËƶÈ:57.1%
Phytochemistry 2008 69 1005-1012
Secondary metabolites from the aerial parts of Salvia palaestina Bentham
Giuseppina Cioffi, Ammar Bader, Anna Malafronte,Fabrizio Dal Piaz, Nunziatina De Tommasi
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
8 . 16-hydroxy-ent-kauranoic acid
ÏàËƶÈ:57.1%
Chinese Chemical Letters 1992 3 435-436
A NEW DITERPENE LACTONE FROM TRIPTERYGUUM WILFORDII
DO QUAN YU,FENG ZHI XIE,XIAO TIAN LIANG
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
9 . glaucocalyxin F
C20H32O4 ÏàËƶÈ:57.1%
Chinese Chemical Letters 2008 19 852-854
Two new diterpenoids from Rabdosia japonica var. glaucocalyx
Zhao Bao Xiang, Yi Xin Xu, Yang Shen, Li Jin, Hou Peng Wang, Hai Sheng Chen
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
10 . sideridiol
ÏàËƶÈ:57.1%
Journal of Natural Products 1990 Vol 53 441
Microbial Transformation of Tetracyclic Diterpenes: Conversion of ent-Kaurenones by Curvularia and Rhizopus Strains
Andres Garcia-Granados, Antonio Martinez, Antonio Ortiz, Maria Esther Onorato, Jose Maria Arias
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
11 . ent-18-hydroxykaur-15-ene-3,7-dione
ÏàËƶÈ:57.1%
Journal of Natural Products 1990 Vol 53 441
Microbial Transformation of Tetracyclic Diterpenes: Conversion of ent-Kaurenones by Curvularia and Rhizopus Strains
Andres Garcia-Granados, Antonio Martinez, Antonio Ortiz, Maria Esther Onorato, Jose Maria Arias
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
12 . compound 4
ÏàËƶÈ:57.1%
Journal of Natural Products 1992 Vol 55 660
Stevisalioside A, a Novel Bitter-Tasting ent-Atisene Glycoside from the Roots of Stevia salicifolia
Rachel Mata, Ver¨®nica Rodr¨ªguez, Rogelio Pereda-Miranda, Norito Kaneda, A. Douglas Kinghorn
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
13 . compound 6
ÏàËƶÈ:57.1%
Journal of Natural Products 1994 Vol 57 811
ent-Kaurane Diterpenoids from Euphorbia wangii
Zhong-Jian Jia, Jian-Gong Shi, Li Yang
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
14 . sideridiol
C20H32O2 ÏàËƶÈ:57.1%
Natural Product Research 2011 Vol. 25, No. 16 1512-1523
Antioxidant activity and chemical composition of Sideritis libanotica Labill. ssp. linearis (Bentham) Borm. (Lamiaceae)
Ibrahim Demirtas, Bulent Ayhan, Ayse Sahin, H¨¹seyin Aksit, Mahfuz Elmastas and Isa Telcib
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
15 . 16¦Á-hydroxy-ent-kauranoic acid
ÏàËƶÈ:57.1%
Phytochemistry 1985 24 2736-2738
15-Hydroxy-acetylerioflorin and other constituents from Viguiera linearis
Guillermo Delgado, Laura Alvarez, Alfonso Romo de Vivar
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
16 . pinusenoid
C20H32O6 ÏàËƶÈ:57.1%
Chemistry of Natural Compounds 2010 46 227-229
Diterpenoid acids from Pinus koraiensis
X. Yang, Y. C. Zhang, H. Zhang, A. J. Dong and H. T. Zhao, et al.
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
17 . ent-3¦Â-butanoyloxykaur-15-en-17-ol
C24H4N1O3 ÏàËƶÈ:57.1%
Bioscience, Biotechnology, and Biochemistry 2011 75 1386-1388
Neuroprotective Kaurane Diterpenes from Fritillaria ebeiensis
Jing XU, Ping GUO, Cuizhou LIU, Zhanping SUN, Liping GUI, Yuanqiang GUO, Tohru YAMAKUNI and Yasushi OHIZUMI
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
18 . compound 34
C21H32O2 ÏàËƶÈ:57.1%
Bioorganic & Medicinal Chemistry 2010 18 1724-1735
Synthesis and induction of apoptosis signaling pathway of ent-kaurane derivatives
Idaira Hueso-Falc¨®n, Natalia Gir¨®n, Pilar Velasco, Juan M. Amaro-Luis, Angel G. Ravelo, Beatriz de las Heras, Sonsoles Hortelano, Ana Estevez-Braun
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
19 . elisapterosin A
C20H28O5 ÏàËƶÈ:57.1%
The Journal of Organic Chemistry 2000 65 1390-1398
Novel Terpenoids from the West Indian Sea Whip Pseudopterogorgia elisabethae (Bayer). Elisapterosins A and B: Rearranged Diterpenes Possessing an Unprecedented Cagelike Framework1
Abimael D. Rodr¨ªguez, Catherine Ram¨ªrez, Ileana I. Rodr¨ªguez, and Charles L. Barnes
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
20 . (+)-(1S,3R,4R,4aS,8aS)-4-(3S)-3-hydroxy-3-methyl-4-pentenyl)-3,4a,8,8-tetramethyldecahydro-1,3-naphthalenediol
C20H34O2 ÏàËƶÈ:57.1%
Tetrahedron 2001 57 5663-5679
The synthesis of Ambrox®-like compounds starting from (+)-larixol
Marjon G Bolster, Ben J.M Jansen, Aede de Groot
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
21 . (+)-(1S,3R,4R,4aS,8aS)-4-((3S)-3-hydroxy-3-methyl-4-pentenyl)-3,4a,8,8-tetramethyldecahydro-1,3-naphthalenediol
ÏàËƶÈ:57.1%
Tetrahedron 2001 57 8369-8379
The synthesis of Ambrox®-like compounds starting from (+)-larixol. Part 2
Marjon G Bolster, B¨¦atrice M.F Lagnel, Ben J.M Jansen, Christophe Morin, Aede de Groot
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
22 . 16¦Á-hydroxy-ent-kauran-19-oic acid
ÏàËƶÈ:57.1%
Journal of the Chinese Chemical Society 2004 51 869-876
Chemical Constituents from Annona glabra
Tian-Jye Hsieh, Yang-Chang Wu, Su-Ching Chen,Ching-Shan Huang and Chung-Yi Chen*
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
23 . Ethyl (15¦Â,16¦Á)-16-(Nitrooxy)-15-[(nitrooxy)methyl]beyeran-18-oate
C23H36N2O8 ÏàËƶÈ:56.5%
Helvetica Chimica Acta 2010 93 2052-2069
Stereoselective Synthesis, Characterization, and Antibacterial Activities of Novel Isosteviol Derivatives with D-Ring Modification
Ya Wu, Cong-Jun Liu, Xu Liu, Gui-Fu Dai, Jin-Yu Du and Jing-Chao Tao
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
24 . 17-acetoxy-16¦Â-ent-kauran-19-oic acid
ÏàËƶÈ:54.5%
Journal of Natural Products 1996 59 635-637
Identification of ent-16¦Â, 17-Dihydroxykauran-19-oic Acid as an Anti-HIV Principle and Isolation of the New Diterpenoids Annosquamosins A and B from Annona squamosa
Yang-Chang Wu, Yu-Chun Hung, Fang-Rong Chang, Mark Cosentino, Hui-Kang Wang, and Kuo-Hsiung Lee
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
25 . ent-17¦Á-acetyl-16¦Â-hydroxyl-kauran-3-one
ÏàËƶÈ:54.5%
Natural Product Research 2008 22 1163-1168
Terpenoids from Chloranthus multistachys
Sheng-Ping Yang; Jian-Min Yue
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
26 . ent-18-acetoxykaur-15-ene-3,7-dioe
C22H30O4 ÏàËƶÈ:54.5%
Journal of Natural Products 1990 Vol 53 441
Microbial Transformation of Tetracyclic Diterpenes: Conversion of ent-Kaurenones by Curvularia and Rhizopus Strains
Andres Garcia-Granados, Antonio Martinez, Antonio Ortiz, Maria Esther Onorato, Jose Maria Arias
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
27 . 11¦Â-acetoxykaurensaure
C23H34O4 ÏàËƶÈ:54.5%
Phytochemistry 1978 17 1917-1922
Neue diterpene und sesquiterpene aus s¨¹dafrikanischen Helichrysum-arten
Ferdinand Bohlmann, Christa Zdero, Evelyn Hoffmann, Pradip Kumar Mahanta, Wolfgang Dorner
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
28 . compound 14b
C22H34O4 ÏàËƶÈ:54.5%
Bioorganic & Medicinal Chemistry 2009 17 1464-1473
Stereoselective synthesis of bioactive isosteviol derivatives as ¦Á-glucosidase inhibitors
Ya Wu, Jing-Hua Yang, Gui-Fu Dai, Cong-Jun Liu, Guo-Qiang Tian, Wen-Yan Ma, Jing-Chao Tao
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
29 . 17-acetoxy16¦Â-ent-kauran-19-oic acid
ÏàËƶÈ:54.5%
Journal of the Chinese Chemical Society 1997 44 313-319
The Constituents from the Stems of Annona cherimola
ê?ÖÐÒ»(Chung-Yi Chen);?ˆ·¼˜s(Pang-Rong Chang);…ÇÓÀ²ý(Yang-Chang Wu)
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
30 . 15,16-epoxy-2-hydroxy-kauran-1-en-3-one
C20H28O3 ÏàËƶÈ:52.3%
Phytochemistry 2004 65 1291-1298
Antibacterial diterpenes and their fatty acid conjugates from rice leaves
Yoshiki Kono, Aya Kojima, Rieko Nagai, Manabu Watanabe,Takahiro Kawashima, Tsugu Onizawa, Tohru Teraoka, Minoru Watanab,Hiroyuki Koshino, Jun Uzawa, Yoshikatsu Suzuki, Akira Sakurai
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
31 . 18-hydroxystemaran-19-oicac id
ÏàËƶÈ:52.3%
Phytochemistry 2002 59 57-62
Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142
Avril R.M. Chen, Paul B. Reese
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
32 . cussovantonin A
C20H32O5 ÏàËƶÈ:52.3%
Phytochemistry 2002 61 367-372
ent-Kaurane diterpenoid glycosides from a Malagasy endemic plant, Cussonia vantsilana
Liva Harinantenaina, Ryoji Kasai, Kazuo Yamasaki
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
33 . cussovantonin B
C20H32O5 ÏàËƶÈ:52.3%
Phytochemistry 2002 61 367-372
ent-Kaurane diterpenoid glycosides from a Malagasy endemic plant, Cussonia vantsilana
Liva Harinantenaina, Ryoji Kasai, Kazuo Yamasaki
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
34 . ent-7¦Â-hydroxy-15¦Â,16¦Â-epoxykauran-19-oic acid
C20H30O4 ÏàËƶÈ:52.3%
Journal of Natural Products 2004 67 614-621
Further Labdane and Kaurane Diterpenoids and Other Constituents from Plectranthus fruticosus
Cristina Gaspar-Marques, M. Ftima Simes, and Benjamn Rodrguez
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
35 . 9¦Â,18-dihydroxy-7¦Á,8¦Á-epoxy-13-epi-entpimara-15-ene
C20H32O3 ÏàËƶÈ:52.3%
Journal of Natural Products 2003 66 392-397
Microbial Transformation of 18-Hydroxy-9,13-epi-ent-pimara-7,15-diene by Gibberella fujikuroi
Braulio M. Fraga, Pedro Gonzlez, Melchor G. Hernndez, Mara C. Chamy, and Juan A. Garbarino
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
36 . ent-15¦Â,16¦Â-epoxykauran-19-oic acid
C20H30O3 ÏàËƶÈ:52.3%
Journal of Natural Products 2003 66 491-496
Labdane and Kaurane Diterpenoids from Plectranthus fruticosus
Cristina Gaspar-Marques, M. Ftima Simes, Aida Duarte, and Benjamn Rodrguez
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
37 . methyl ent-15¦Â,16¦Â-epoxykauran-19-oate
C21H32O3 ÏàËƶÈ:52.3%
Journal of Natural Products 2003 66 491-496
Labdane and Kaurane Diterpenoids from Plectranthus fruticosus
Cristina Gaspar-Marques, M. Ftima Simes, Aida Duarte, and Benjamn Rodrguez
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
38 . ethyl 17-Norabiet-13(15)-Z-en-8¦Â-ol-16-oate
C21H34O3 ÏàËƶÈ:52.3%
Journal of Natural Products 2007 70 1253-1258
Transformations of Manool. Tri- and Tetracyclic Norditerpenoids with in Vitro Activity against Plasmodium falciparum
Albert W. W. van Wyk,Kevin A. Lobb, Mino R. Caira, Heinrich C. Hoppe, and Michael T. Davies-Coleman
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
39 . methyl 7¦Â,15¦Á-dihydroxy-ent-kau¦Á-16-en-19-oate
C21H32O4 ÏàËƶÈ:52.3%
Journal of Natural Products 2001 64 222-225
Microbial Transformation of ent-Kaurenoic Acid and Its 15-Hydroxy Derivatives by the SG138 Mutant of Gibberella fujikuroi
Alejandro F. Barrero, J. Enrique Oltra, Enrique Cerd¨¢-Olmedo, Javier Ávalos, and Jos¨¦ Justicia
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
40 . 8-oxo-8,14-seco-abiet-12-en-14,19-dial
C20H30O3 ÏàËƶÈ:52.3%
Journal of Natural Products 2001 64 511-514
Diterpenoids from the Leaves of Juniperus chinensis var. kaizuka
Ching-Kuo Lee, and Yu-Shia Cheng
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
41 . 15-oxolabda-8(17),11(Z),13(Z)-trien-19-oic acid
C20H28O3 ÏàËƶÈ:52.3%
Journal of Natural Products 2000 63 1381-1383
Labdane-Type Diterpenes and a Nordrimane-Type Sesquiterpene from the Stem Bark of Thuja standishii
Manabu Iwamoto, Hironori Ohtsu, Shunyo Matsunaga, and Reiko Tanaka
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
42 . 16¦Á-methoxy-entkauran-19-oic acid
ÏàËƶÈ:52.3%
Journal of Natural Products 2000 63 1000-1003
ent-Kaurane Diterpenoids from Annona glabra
Chung-Yi Chen, Fang-Rong Chang, Chun-Ping Cho, and Yang-Chang Wu
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
43 . (4S,5¦Á,8S,9¦Á,10S,13R)-9,13-epoxy-14-labden-19-oic acid
C20H32O3 ÏàËƶÈ:52.3%
Journal of Natural Products 2000 63 226-229
Grindelane Diterpenoids from Stevia subpubescens
Luisa U. Rom¨¢n, Jairo I. Cambr¨®n, Rosa E. del R¨ªo, Juan D. Hern¨¢ndez, Carlos M. Cerda-Garc¨ªa-Rojas, and Pedro Joseph-Nathan
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
44 . ent-13-norisocopalen-15-al-18-oic acid
C19H28O3 ÏàËƶÈ:52.3%
Journal of Natural Products 2000 63 422-423
Two New Spongian Diterpenes from Coscinoderma mathewsi
Mitsumasa Hyosu and Junji Kimura
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
45 . ent-3¦Â,16¦Á,17-trihydroxyatis-13-en-11-one
C20H30O4 ÏàËƶÈ:52.3%
Journal of Natural Products 1997 60 86-92
Biotransformation of ent-Atisenes and ent-Beyerenes by Rhizopus nigricans and Fusarium moniliforme Cultures
Andr¨¦s Garc¨ªa-Granados, Andr¨¦s Parra, and Jos¨¦Mar¨ªa Arias
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
46 . syspirensin B
C20H36O5 ÏàËƶÈ:52.3%
Journal of Natural Products 1996 59 457-460
Neoclerodane Diterpenoids from Teucrium chamaedrys subsp. Syspirense
Ihsan Çalis and Erdal Bedir, Anthony D. Wright and Otto Sticher
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
47 . 17-hydroxy-16¦Â-ent-kauran-19-al
ÏàËƶÈ:52.3%
Journal of Natural Products 1996 59 635-637
Identification of ent-16¦Â, 17-Dihydroxykauran-19-oic Acid as an Anti-HIV Principle and Isolation of the New Diterpenoids Annosquamosins A and B from Annona squamosa
Yang-Chang Wu, Yu-Chun Hung, Fang-Rong Chang, Mark Cosentino, Hui-Kang Wang, and Kuo-Hsiung Lee
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
48 . 3¦Á,8¦Á, 15,16-tetrahydroxy-ent-pimarane
ÏàËƶÈ:52.3%
Planta Medica 1988 54 533-537
Unusual Norhomoditerpenes and Other Constituents from Kyrsteniopsis dibollii
J. Jakupovic, H. Klemeyert, F. Bohlmannt, and A. Whittemore
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
49 . ent-7¦Á,11¦Â-dihydroxy-kaur-16-en-19-oic acid
C20H30O4 ÏàËƶÈ:52.3%
Phytochemistry 2009 70 2017-2022
Hydroxylation of the diterpenes ent-kaur-16-en-19-oic and ent-beyer-15-en-19-oic acids by the fungus Aspergillus niger
Silvia Marquina, Jos¨¦ Luis Parra, Manas¨¦s Gonz¨¢lez, Alejandro Zamilpa, Jaime Escalante, Mar¨ªa R. Trejo-Hern¨¢ndez, Laura Álvarez
Structure 13C NMR ̼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------
50 . methyl-ent-7¦Á,11-dihydroxykaur-16-en-19-oate
C21H32O4 ÏàËƶÈ:52.3%
Phytochemistry 2009 70 2017-2022
Hydroxylation of the diterpenes ent-kaur-16-en-19-oic and ent-beyer-15-en-19-oic acids by the fungus Aspergillus niger
Silvia Marquina, Jos¨¦ Luis Parra, Manas¨¦s Gonz¨¢lez, Alejandro Zamilpa, Jaime Escalante, Mar¨ªa R. Trejo-Hern¨¢ndez, Laura Álvarez
Structure 13C NMR ̼Æ×Ä£Äâͼ |
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