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30.96,53,56.01,56.09,63.93,88.98,108.7,112.17,114.44,118.12,119.46,126.5,128.17,129.02,132.18,144.84,145.95,146.73,151.52,153.02,193.56
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1 .     balanophonin
    ÏàËÆ¶È:95.2%
Chemical & Pharmaceutical Bulletin          1982          30          1525-1527
BALANOPHONIN, A NEW NEO-LIGNAN FROM BALANOPHORA JAPONICA MAKINO
Mitsumasa Haruna,Tomoko Koube,Kazuo Ito and Hiroyuki Murata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     melianoninol
C20H20O6     ÏàËÆ¶È:95.2%
Journal of Chinese Pharmaceutical Sciences          1992          1          7-11
Studies on the Chemical Constituents of Melia azedarach
Ren-Sheng Xu; Wen-Han Lin; Jiu Han; Wen-Lu Wang; Shan-Huan Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     melianoninol
C20H20O6     ÏàËÆ¶È:95.2%
Acta Pharmaceutica Sinica          1991          26          426-429
STUDIES ON THE CHEMICAL CONSTITUENTS OF MELIA AZEDARACH L.
J Han; WH Lin; RS Xu; WL Wang and SH Zhao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     balanophonin
C20H20O6     ÏàËÆ¶È:95.2%
Phytochemistry          1999          50          781-785
Coniferaldehyde derivatives from tissue culture of Artemisia annua and Tanacetum parthenium
Lai-King Sy, Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 6
    ÏàËÆ¶È:95.2%
Chinese Pharmaceutical Journal          2002          37          14-17
Study on chemical constituents isolated from Glycosmis citrifolia
SHEN Xiao-Ling, ZENG Hui-Fang, CHEN Zhen, ZHONG Guang-Hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (E)-3-[(2S,3R)-2,3-dihydro-2-(4'-hydroxy-3'-methoxyphenyl)-3-hydroxymethyl-7-methoxy-1-benzofuran-5-yl]-2-propenal
C20H20O6     ÏàËÆ¶È:95.2%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (E)-3-[(2R,3S)-2,3-dihydro-2-(4'-hydroxy-3'-methoxyphenyl)-3-hydroxyemthyl-7-methoxy-1-benzofuran-5-yl]-2-propenal
C20H20O6     ÏàËÆ¶È:95.2%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Curcasinlignan A
C20H20O6     ÏàËÆ¶È:95.2%
Zeitschrift f¨¹r Naturforschung B          2012          67          176-180
New Lignans from Jatropha curcas Linn.
J. J. Xu and N. H. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     Balanophonin
C20H20O6     ÏàËÆ¶È:95.2%
Plant Diversity and Resources          2013          35          209-215
Antioxidant Constituents from Pinus massoniana (Pinaceae)
ZHANG Yu-Mei, GONG Qing-Fang, YANG Jia-Qian, ZENG Guang-Zhi, TAN Ning-Hua
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     balanophonin
    ÏàËÆ¶È:95.2%
Chinese Traditional and Herbal Drugs          2013          44          1717-1720
Chemical constituents from Xanthii Fructus
CHEN Jie, WANG Rui, SHI Yan-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     Balanophonin
C20H20O6     ÏàËÆ¶È:95.2%
Chinese Journal of Applied & Environmental Biology          2014          20          245-248
Chemical constituents of stir-fried Melia toosendanfruits
YANG Ming, LI Fu, WAN Li & WANG Mingkui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (9S*,10S*)-3-[7-(3,10-dihydroxy-9-hydroxymethyl-2,5-dimethoxy)-9,10-dihydrophenanthrenyl]propenal
C20H20O6     ÏàËÆ¶È:90.4%
Journal of Natural Products          2001          64          832-835
New Dihydrophenanthrene and Phenyldihydroisocoumarin Constituents of Trema orientalis
M.-Genevi¨¨ve Dijoux-Franca,Diderot Noungou¨¦ Tchamo, Bruno Cherel, Max Cussac, Etienne Tsamo, and Anne-M. Mariotte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (-)-balanophonin
C20H20O6     ÏàËÆ¶È:90.4%
Korean Journal of Pharmacognosy          2001          32(4)          302-306
Chemical Components from the Stem Barks of Kalopanax septemlobus
Hong, Sung-Su; Han, Doo-Il; Hwang, Bang-Yeon; Choi, Woo-Hoi; Kang, Ho-Sang; Lee, Myung-Koo; Lee, Don-Koo; Lee, Kyong-Soon; Ro, Jai-Seup
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     Balanophonin
    ÏàËÆ¶È:90.4%
Molecules          2010          15          4011-4016
Aquilarin A, a New Benzenoid Derivative from the Fresh Stem of Aquilaria sinensis
Qing-Huang Wang, Ke Peng, Le-He Tan and Hao-Fu Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Balanophonin
C20H20O6     ÏàËÆ¶È:90.4%
Molecules          2011          16          10157-10167
Antioxidant Phenolic Compounds of Cassava (Manihot esculenta) from Hainan
Bo Yi, Lifei Hu, Wenli Mei, Kaibing Zhou, Hui Wang, Ying Luo, Xiaoyi Wei and Haofu Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     9,10-threo-3-[7-(3,10-dihydroxy-9-hydroxymethyl-2,5-dimethoxy)-9,10-dihydrophenanthrenyl]propenal
C20H20O6     ÏàËÆ¶È:90.4%
Journal of Chemistry          2009          47          716-719
Isoflavones and dihydrophenanthrene from Dalbergia tonkinensis.
Trần Anh Tuấn, Nguyễn Tiến Đạt, Nguyễn Ho¨¤i Nam
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     balanophonin
    ÏàËÆ¶È:90.4%
Natural Product Research and Development          2010          22          945-948
Lignans from the Stem of Schima superba
XU Wen; ZHOU Guang-xiong; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     balanophonin
    ÏàËÆ¶È:90.4%
Chinese Journal of Natural Medicines          2011          9          112-114
Chemical Constituents from Dragon's Blood of Dracaena cambodiana
LUO Ying,, DAI Hao-Fu, WANG Hui, MEI Wen-Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     siraitiflavandiol
C20H20O6     ÏàËÆ¶È:80.9%
Journal of Asian Natural Products Research          2009          11          761-765
A new antibacterial compound from Luo Han Kuo fruit extract (Siraitia grosvenori)
Yan Zheng, Zhonglian Liu, Jeff Ebersole and Chifu Brad Huang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (E)-3-[(2S,3R)-2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(3',4'-dimethoxyphenyl)-1-benzofuran-5-yl]-2-propenal
C21H22O6     ÏàËÆ¶È:80.9%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (E)-3-[(2R,3S)-2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(3',4'-dimethoxyphenyl)-1-benzofuran-5-yl]-2-propenal
C21H22O6     ÏàËÆ¶È:80.9%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     cassyformin
C20H20O7     ÏàËÆ¶È:80.9%
Journal of the Chinese Chemical Society          2004          51          221-223
Neolignans from the Parasitic Plants. Part 2. Cassytha filiformis
Jiau-Ching Ho, Chiu-Ming Chen and Lie-Ching Row*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     xylobuxin
C21H22O7     ÏàËÆ¶È:76.1%
Journal of Natural Products          1995          Vol 58          786-789
Isolation and Structure Elucidation of Xylobuxin, a New Neolignan from Xylopia buxifolia
Anne Wahl, François Roblot, Andr¨¦ Cav¨¦
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     (E)-3-[(2R,3S)-2,3-dihydro-3-hydroxym;ethyl-7-methoxy-2-(3'-methoxy-4'-methoxymethoxyphenyl)-1-benzofuran-5-yl]-2-propenal
C22H24O7     ÏàËÆ¶È:76.1%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     methyl (E)-3-[(2S,3R)-2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(4'-hydroxy-3'-methoxyphenyl)-1-benzofuran-5-yl]-propenoate
C21H22O7     ÏàËÆ¶È:76.1%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     4-O-methylbalanophonin
C21H22O6     ÏàËÆ¶È:76.1%
Journal of the Chinese Chemical Society          2004          51          221-223
Neolignans from the Parasitic Plants. Part 2. Cassytha filiformis
Jiau-Ching Ho, Chiu-Ming Chen and Lie-Ching Row*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     compound 7
    ÏàËÆ¶È:76.1%
Chinese Journal of Natural Medicines          2012          10          358-362
A new 1, 10-secoguaianolide from the aerial parts of Artemisia anomala
Ke ZAN, Xiao-Qing CHEN, Peng-Fei TU
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     9-isovaleroxy balanophonin
C25H28O7     ÏàËÆ¶È:76%
Bioorganic & Medicinal Chemistry          2013          21          7074-7082
N-Alkyl dien- and trienamides from the roots of Otanthus maritimus with binding affinity for opioid and cannabinoid receptors
Stefania Ruiu, Nicola Anzani, Alessandro Orr¨´, Costantino Floris, Pierluigi Caboni, Elias Maccioni, Simona Distinto, Stefano Alcaro, Filippo Cottiglia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     3-acetoxymethyl-5-[(E)-2-formylethen-1-yl]-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dihydrobenzofuran
C22H22O7     ÏàËÆ¶È:72.7%
Journal of Natural Products          1998          61          771-775
Lignans from Chilean Propolis
Susanne Valcic, Gloria Montenegro, and Barbara N. Timmermann
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     (E)-3-[(2S,3R)-2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(3'-methoxy-4'-methoxymethoxyphenyl)-1-benzofuran-5-yl]-2-propenal
C22H24O7     ÏàËÆ¶È:72.7%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     erythro-guaiacylglycerol-¦Â-coniferyl aldehyde ether
C20H22O7     ÏàËÆ¶È:71.4%
Chemistry of Natural Compounds          2009          45          536-538
CHEMICAL CONSTITUENTS FROMTHE STEM BARK OF Trewia nudiflora
Shao-Hua Wu, Yue-Mao Shen, You-Wei Chen, Zhi-Ying Li, Li-Yuan Yang, and Shao-Lan Li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     balanophonin
    ÏàËÆ¶È:71.4%
China Journal of Chinese Materia Medica          2009          34          1687-1689
Chemical constituents from Xanthium mongolicum
ZHANGWenzhi, HAN Wei, LI Ying, ZHANG Shujun, ZHAO Defeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     balanophonin
C20H20O6     ÏàËÆ¶È:71.4%
Journal of Shenyang Pharmaceutical University          2006          23          209-211
Chemical constituents of Nux Prinsepiae Uniflorae
LI Hong-xuan, LI Xian, WANG Jin-hui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     balanophonin
    ÏàËÆ¶È:71.4%
Chinese Jouranl of Magnetic Resonance          1997          14          425-429
THE STUDIES ON THE NMR SPECTRA OF DIHYDROBENZOFURAN LIGNANS
Gao Feng, Li Xian, Wu Lijun and Li Wen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     pinnatifidanin C II
C20H22O8     ÏàËÆ¶È:71.4%
Fitoterapia          2013          91          217-223
Cytotoxic and antioxidant dihydrobenzofuran neolignans from the seeds of Crataegus pinnatifida
Xiao-Xiao Huang, Chen-Chen Zhou, Ling-Zhi Li, Ying Peng, Li-Li Lou, Sen Liu, Dian-Ming Li, Takshi Ikejima, Shao-Jiang Song
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     Curcasinlignan B
C18H18O6     ÏàËÆ¶È:71.4%
Zeitschrift f¨¹r Naturforschung B          2012          67          176-180
New Lignans from Jatropha curcas Linn.
J. J. Xu and N. H. Tan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     dihydrodehydrodiconifenyl alcohol
    ÏàËÆ¶È:66.6%
Journal of Asian Natural Products Research          2008          10          499-502
One new dihydrobenzofuran lignan from Vitex trifolia
Qiong Gu, Xue-Mei Zhang, Jun Zhou, Sheng-Xiang Qiu and Ji-Jun Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     hyoscyamal
C20H18O6     ÏàËÆ¶È:66.6%
Natural Product Research          2009          23          595-600
Hyoscyamal, a new tetrahydrofurano lignan from Hyoscyamus niger Linn.
A. Sajeli Begum; Shweta Verma; Mahendra Sahai; Kathrin Schneider; Roderich S¨¹ssmuth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     (-)-Balanophonin
    ÏàËÆ¶È:66.6%
Archives of Pharmacal Research          2007          30          402-407
Lignans from the fruits of cornus kousa burg. and their cytotoxic effects on human cancer cell lines
Dae-Young Lee, Myoung-Chong Song, Ki-Hyun Yoo, Myun-Ho Bang and In-Sik Chung, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     (7R,8S)-ficusal
    ÏàËÆ¶È:66.6%
Chinese Pharmaceutical Journal          2010          45          650-653
Study on Lignans from Catunaregam spinosa
GAO Guang-chun, TAO Shu-hong, ZHANG Si, LI Qing-xin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     (+)-dihdyrodehydrodiconiferyl alcohol
    ÏàËÆ¶È:66.6%
Natural Product Research and Development          2008          20          257-261
Chemical Constituents of Keteleeria evelyniana
FU Zhao-hui;ZHANG Yu-mei; TAN Ning-hua; CHU Hong-biao; JI Chang-jiu;
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     methyl (E)-3-[(2R,3S)-2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(3'-methoxy-4'-methoxy-methoxyphenyl)-1-benzofuran-5-yl]-propenoate
C23H26O8     ÏàËÆ¶È:66.6%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     (E)-3-[(2S,3R)-2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(4'-hydroxy-3'-methoxyphenyl)-1-benzofuran-5-yl]-2-propen-1-ol
    ÏàËÆ¶È:66.6%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     (E)-3-[(2R,3S)-2,3-dihydro-3-hydroxymethyl-7-methoxy-2-(4'-hydroxy-3'-methoxyphenyl)-1-benzofuran-5-yl]-2-propen-1-ol
    ÏàËÆ¶È:66.6%
Tetrahedron          1998          54          12429-12444
On the absolute structure of optically active neolignans containing a dihydrobenzofuran skeleton
Mabel S.M. Yuen, Feng Xue, Thomas C.W. Mak, Henry N.C. Wong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     È¥ÇâË«Ëɰش¼
    ÏàËÆ¶È:66.6%
Jiangxi Journal of Traditional Chinese Medicine          2013          44          54-54
´¨µ³²ÎÖеÄ1¸öÄ¾Ö¬ËØÀà³É·Ö
²ÜÀò, »Æ¶àÁÙ
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     compound 18
C22H21O8     ÏàËÆ¶È:63.6%
Journal of the American Chemical Society          2009          131          1745-1752
Explorations into Neolignan Biosynthesis: Concise Total Syntheses of Helicterin B, Helisorin, and Helisterculin A from a Common Intermediate
Scott A. Snyder and Ferenc Kontes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     Ethyl 3-[2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxylmethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl] propanoate
C22H26O7     ÏàËÆ¶È:63.6%
Natural Product Communications          2010          5          1627 - 1630
Two Pairs of Enantiomeric Neolignans fromLobelia chinensis
Jian-Xin Chen, Shen-Hui Huang, Lei Wanga, Wei-Li Han, Ying Wang, Dong-Mei Zhangand Wen-Cai Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     3-[2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxylmethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl acetate
C22H26O7     ÏàËÆ¶È:63.6%
Natural Product Communications          2010          5          1627 - 1630
Two Pairs of Enantiomeric Neolignans fromLobelia chinensis
Jian-Xin Chen, Shen-Hui Huang, Lei Wanga, Wei-Li Han, Ying Wang, Dong-Mei Zhangand Wen-Cai Ye
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     lawsonicin
C20H24O6     ÏàËÆ¶È:61.9%
Helvetica Chimica Acta          2003          Vol. 86          2164
Two New and a Known Compound from Lawsonia inermis
Bina S. Siddiqui, M. Nadeem Kardar, S. Tariq Ali, and Shazia Khan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     dihydrodehydrodiconiferyl alcohol
    ÏàËÆ¶È:61.9%
Phytochemistry          2000          55          597-601
nor-Lignans from the leaves of Styrax ferrugineus (Styracaceae) with antibacterial and antifungal activity
Patricia Mendonça Pauletti, Angela Regina Ara¨²joa, Maria Claudia Marx Young, Astr¨¦a M. Giesbrecht, Vanderlan da Silva Bolzani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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