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Gaoyumeng: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-10 15:44:18
1 .     3-heptadecyl-5-methoxy-phenol
C24H42O2     ÏàËÆ¶È:61.1%
Journal of Ethnopharmacology          2003          88          241-247
Bioactive alkyl phenols and embelin from Oxalis erythrorhiza
Gabriela Egly Feresin, Alejandro Tapia, Maximiliano Sortino, Susana Zacchino, Antonieta Rojas de Arias, Alba Inchausti, Gloria Yaluff, Jaime Rodriguez, Cristina Theoduloz, Guillermo Schmeda-Hirschmann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     eleocharinol A
    ÏàËÆ¶È:61.1%
Natural Product Research and Development          2013          25          1615-1620
Phenolic Constituents and Antioxidant Activity of Eleocharis tuberosa Peels
LI Xing-ren, LUO Yang-he*, HE Juan, PENG Li-yan, WU Xing-de, DU Ru-nan, ZHAO Qin-shi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     5-Pentyl-3-methoxy-N-butylaniline
    ÏàËÆ¶È:55.5%
Phytochemistry          2009          70          1233-1238
Anti-mosquito and antimicrobial nor-halimanoids, isocoumarins and an anilinoid from Tessmannia densiflora
Charles Kihampa, Mayunga H.H. Nkunya, Cosam C. Joseph, Stephen M. Magesa, Ahmed Hassanali, Matthias Heydenreich , Erich Kleinpeter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3,4-dihydro-6,8-dimethoxxy-3-(2-hydroxypentyl)isocoumarin
C16H22O5     ÏàËÆ¶È:55.5%
Journal of Natural Products          2010          73          75-78
An Antimycobacterial Cyclodepsipeptide from the Entomopathogenic Fungus Ophiocordyceps communis BCC 16475
Rachada Haritakun, Malipan Sappan, Rapheephat Suvannakad, Kanoksri Tasanathai and Masahiko Isaka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (+)-4-((1S,4S,4aS,8aR)-4-hydroxy-5,5,8a-trimethyl-2-methylenedecahydro-1-naphthalenyl)-2-butanone
C18H30O2     ÏàËÆ¶È:55.5%
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   Ì¼Æ×Ä£Äâͼ
6 .     (+)-4-((1S,4S,4aS,8aR)-4-hydroxy-5,5,8a-trimethyl-2-methylenedecahydro-1-naphthalenyl)-2-butanone
C18H28O     ÏàËÆ¶È:55.5%
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   Ì¼Æ×Ä£Äâͼ
7 .     compound 4c
    ÏàËÆ¶È:55.5%
Magnetic Resonance in Chemistry          1997          35          821-828
Configurational and conformational study of new esters derived from 2-methyl-2-azabicyclo[2.2.2]octan-5-syn(anti)-ols by NMR spectroscopy and x-ray crystallography¡ªI
M. J. Fern¨¢ndez, R. Huertas, M. S. Toledano, E. G¨¢lvez, J. Server and M. Mart¨ªnez-Ripoll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (10'R)-5-(10-hydroxytridecyl)-1-O-methylresorcinol
C20H34O3     ÏàËÆ¶È:55%
Phytochemistry          1994          36          189-194
Resorcinol derivatives and other components from Ononis viscosa subsp. breviflora
Alejandro.F. Barrero, Eduardo Cabrera, Ignacio Rodr¨ªguez, Eva M. Fern¨¢ndez-Gallego
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     compound 1
C27H38O11     ÏàËÆ¶È:55%
Journal of Shenyang Pharmaceutical University          2008          25          964-966
New diterpene from the seeds of Caesalpinia minax Hance
WU Zhao-hua, WANG Li-bo, GAO Hui-yuan, SUN Bo-hang, HUANG Jian, WU Li-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     11-hydroxytubotaiwine
C20H24N2O3     ÏàËÆ¶È:55%
Heterocycles          1994          38          2411-2414
Isolation of Two New Nitrogenous Metabolites from the Cultured Cells of Aspidosperma Quebracho-Blanco
Norio Aimi, Naoki Uchida, Naoko Oya, Shin-ichiro Sakai, Luis A. Mendonza, Peter Obitz, and Joachim Stöckigt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 27
    ÏàËÆ¶È:52.6%
Tetrahedron Letters          2000          41          6643-6647
An enantiospecific approach to thapsanes from R-carvone: synthesis of (−-thaps-8-en-5-ol
A. Srikrishna, K. Anebouselvy, T. Jagadeeshwar Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (1R,2R,6R,7R)-2-(tert-butyldimethylsilyloxy)-1,5,5,6,7-pentamethyl-8-methylenebicyclo[4.3.0]nonane
C21H40OSi     ÏàËÆ¶È:52.6%
Indian Journal of Chemistry Section B          2008          47B          449-459
Enantiospecific synthesis of thaps-8-en-5-ol via stereospecific
Srikrishna,A; Anebouselvy,K
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (1R*,3aS*,9bR*)-1-isopropyl-6-methoxy-3a,8-dimethyl-1,3,3a,4,5,9b-hexahydrocyclopenta[a]naphthalene-2-one
C19H26O2     ÏàËÆ¶È:52.6%
The Journal of Organic Chemistry          2004          69          2773-2784
Synthesis of ((+/-)-Hamigeran B, (-)-Hamigeran B, and ((+/-)-1-epi-Hamigeran B: Use of Bulky Silyl Groups to Protect a Benzylic Carbon-Oxygen Bond from Hydrogenolysis
Derrick L. J. Clive and Jian Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     isodonhenrin C
C21H30O7     ÏàËÆ¶È:52.3%
Chemical & Pharmaceutical Bulletin          2011          59          1562-1566
Cytotoxic ent-Kaurane Diterpenoids from Isodon henryi
Zhuo Hu, Rui Zhan, Xue Du, Jia Su, Xiao-Nian Li, Jian-Hong Yang, Hai-Bo Zhang, Yan Li, Han-Dong Sun, Gan-Peng Li and Jian-Xin Pu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     11-(3-hydroxy-5-pentylphenoxy)-N0,N0-dimethylundecanehydrazide
C24H42N2O3     ÏàËÆ¶È:52.1%
Bioorganic & Medicinal Chemistry          2014          22          4770-4783
Structure¨Caffinity relationships and pharmacological characterization of new alkyl-resorcinol cannabinoid receptor ligands: Identification of a dual cannabinoid receptor/TRPA1 channel agonistOriginal Research Article
Antonella Brizzi, Francesca Aiello, Pietro Marini, Maria Grazia Cascio, Federico Corelli, Vittorio Brizzi, Luciano De Petrocellis, Alessia Ligresti, Livio Luongo, Stefania Lamponi, Sabatino Maione, Roger G. Pertwee, Vincenzo Di Marzo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     stilbostemin N
C16H18O3     ÏàËÆ¶È:50%
Phytochemistry          2008          69          457-463
Antibacterial stilbenoids from the roots of Stemona tuberosa
Li-Gen Lin, Xin-Zhou Yang, Chun-Ping Tang, Chang-Qiang Ke, Ji-Bao Zhang, Yang Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     stereumin C
C16H22O4     ÏàËÆ¶È:50%
Phytochemistry          2008          69          1439-1445
Stereumin A¨CE, sesquiterpenoids from the fungus Stereum sp. CCTCC AF 207024
Guo-Hong Li, Meng Duan, Ze-Fen Yu, Lei Li, Jin-Yan Dong, Xing-Biao Wang,Jian-Wei Guo, Rong Huang, Min Wang, Ke-Qin Zhang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ravidin A
C20H24O5     ÏàËÆ¶È:50%
Phytochemistry          2004          65          2533-2537
Clerodane-type diterpenoids from Nannoglottis ravida
Hai-Lin Qin, Zhi-Hong Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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