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13C NMR (101 MHz, CDCl3) ¦Ä 17.7, 29.7, 49.5, 56.4, 105.6, 125.6, 126.8, 138.1, 147.4, 153.1, 193.4.

13C NMR (101 MHz, CDCl3) ¦Ä 13.7, 14.1, 19.2, 29.7, 30.6, 56.0, 65.6, 109.4, 114.9, 124.0, 126.5, 126.7, 128.8, 130.9, 132.3, 145.7, 146.9, 148.9, 153.0, 167.7, 193.6.

13C NMR (101 MHz, CDCl3) ¦Ä 11.6, 16.2, 18.2, 21.1, 26.0, 29.7, 31.9, 35.1, 36.3, 41.7, 49.3, 55.9, 67.0, 76.7, 77.0, 77.2, 77.3, 79.0, 107.8, 146.2.
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2
1 .     4-Phenyl-2-thienyl-4H-benzo[f]chromene-3-carbothioic acid O-butyl ester
C28H24O2S2     ÏàËÆ¶È:63.6%
Tetrahedron          2012          68          1247-1252
Highly convergent one-pot four-component regioselective synthesis of 4H-benzo[f]chromenes via annulation of ¦Â-oxodithioesters
Subhasis Samai, Ganesh Chandra Nandi, Maya Shankar Singh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     vitexdoin C
C19H16O5     ÏàËÆ¶È:61.9%
Journal of Natural Products          2009          72          1627-1630
Nitric Oxide Scavenging Lignans from Vitex negundo Seeds
Cheng-Jian Zheng, Bao-Kang Huang, Ting Han, Qiao-Yan Zhang,Hong Zhang, Khalid Rahman, and Lu-Ping Qin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     n-docosyl trans-ferulate
C32H54O4     ÏàËÆ¶È:61.9%
Chemistry of Natural Compounds          2009          45          234-236
MONO-AROMATIC CONSTITUENTSOF Dendrobium longicornu
Jiang-Tao Li, Ben-Lin Yin, Ying Liu, Li-Qin Wang, and Ye-Gao Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     (2E)-2-propenoic acid,3-(4-hydroxy-3-methoxyphenyl)-decosyl ester
    ÏàËÆ¶È:61.9%
China Journal of Chinese Materia Medica          2004          29          147-149
Chemical constituents from the rhizoma of Arundina graminifolia
LIU Meifeng, HAN Yun, XING Dongming, Wang Wei, XU Lizhen, DU Lijun, DING Yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     docosyl ferulate
C32H54O4     ÏàËÆ¶È:61.9%
Acta Pharmaceutica Sinica          1998          Vol 33          350-354
STUDIES ON CHEMICAL CONSTITUENTS OF TINOSPORA HAINANESIS
Guo Youying(Guo YY); Lin Lianbo(Lin LB) and Shen Jing(Shen J)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     4-(2-Chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid bis [3-(3-pyridyl)propyl] ester
C31H32ClN3O4     ÏàËÆ¶È:61.9%
Bioorganic & Medicinal Chemistry          1998          6          2219-2227
Newly synthesized dihydropyridine derivatives as modulators of P-Glycoprotein-mediated multidrug resistance
Hirokazu Tanabe, Shigeyuki Tasaka, Hiromasa Ohmori, Noriaki Gomi, Yoshiyuki Sasaki, Toshiki Machida, Mayumi Iino, Akira Kiue, Seiji Naito, Michihiko Kuwano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     hycandinic acid ester
    ÏàËÆ¶È:61.9%
Natural Product Research and Development          2009          21          593-599
Chemical Constituents of Osmanthus yunnanensis
MA Xiao-li;LIN Wen-bing; ZHANG Guo-lin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     2-(2,4-dichlorophenoxy)ethyl 3-methyl-2¦Î,4E-decadienoate
C19H24ClO3     ÏàËÆ¶È:61.9%
Russian Journal of Organic Chemistry          2001          37          246-255
Synthesis of Analogs of Juvenile Hormons Proceeding from Phenol Derivatives
E.T. Yamansarova, A.G. Kukovinets, O.S. Kukovinets, R.A. Zainullin and F.Z. Galin, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     2-(2,4-dichlorophenoxy)ethyl 3-methyl-2¦Î,4E-undecadienoate
C20H26Cl2O3     ÏàËÆ¶È:61.9%
Russian Journal of Organic Chemistry          2001          37          246-255
Synthesis of Analogs of Juvenile Hormons Proceeding from Phenol Derivatives
E.T. Yamansarova, A.G. Kukovinets, O.S. Kukovinets, R.A. Zainullin and F.Z. Galin, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     deoxypodophyllotoxin
    ÏàËÆ¶È:57.1%
Planta Medica          1997          63          365-366
Antimitotic and Cytotoxic Constituents of Myodocarpus gracilis
A. Montagnac,J. P. Provost, M. Litaudon, and M. Pa?s
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     hexacosylferulate
C36H62O4     ÏàËÆ¶È:57.1%
Natural Product Research          2006          20          775-781
Constituents of Salvia microphylla
Zeynep Aydo?mu?; Volkan Ye??lyurt; G¨¹la?ti Topcu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     pentacosanylferulates
C35H60O4     ÏàËÆ¶È:57.1%
China Journal of Chinese Materia Medica          2007          32          698-700
Studies on chemical constituents from roots of Caragana microphylla
JIN Guangzhu, PIAO Huishun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     octacosyl ferulate
    ÏàËÆ¶È:57.1%
China Journal of Chinese Materia Medica          2001          26          180-182
Studies on Chemical Constituents from Euphorbia fischeriana Steud.
LIU Wenzi, HE Fenglei, RUAN Ziyong, GU Xiongfei, WU Xiaoyun, QIN Guowei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     erythrinasinate
    ÏàËÆ¶È:57.1%
Journal of Natural Products          1989          Vol 52          320
Two New Flavonoids from Erythrina eriotriocha
Augustin E. Nkengfack, Dale R. Sanson, Michael S. Tempesta, Z. Tanee Fomum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     Incarvine C
    ÏàËÆ¶È:57.1%
Phytochemistry          1995          39          1485-1487
Two alkaloids from Incarvillea sinensis
Yu-Ming Chi, Fumio Hashimoto, Wen-Mei-Yan, Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     trans-docosanoylferulate
C32H54O4     ÏàËÆ¶È:57.1%
Phytochemistry          1994          37          1371-1375
Rearranged abietane diterpenes from Teucrium divaricatum subsp. Villosum
Ayhan Ulubelen, G¨¹la?ti Topcu, Sibel Ol?al
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3,4-Dihydro-2,2,7,8-tetramethyl-5-(5-(4-nitrophenyl)-isoxazol-3-yl)-2H-1-benzopyran-6-ol
C22H22N2O5     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry          2011          19          4841-4850
Isoxazole substituted chromans against oxidative stress-induced neuronal damage
Maria Koufaki, Alexandra Tsatsaroni, Xanthippi Alexi, Hel¨¨ne Guerrand, Sofia Zerva Michael N. Alexis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     Ethyl 2-[(4'-methoxy-2,3,6-trimethyl-5-nitro[1,1'-biphenyl]-4-yl)oxy]acetate
C20H23NO6     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry          2011          19          5061-5070
Regulation of the Escherichia coli AtoSC two component system by synthetic biologically active 5;7;8-trimethyl-1;4-benzoxazine analogues
Panagiota S. Filippou, Eftychia N. Koini, Theodora Calogeropoulou, Panagiota Kalliakmani, Christos A. Panagiotidis, Dimitrios A. Kyriakidis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     compound 8d
C23H28N2O4     ÏàËÆ¶È:57.1%
Journal of Heterocyclic Chemistry          2007          44          909-914
A facile synthesis of 1-alkyl-5-arylalkoxy-6-methoxy-3,4-dihydroisoquinolines
Heong-Seup Yim,Ho-Kyun Kim,Jeum-Jong Kim,Deok-Heon Kweon,Yong-Jin Yoon,Sang-Gyeong Lee and Jung-Ho Kim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 8c/2
C21H19Cl2N3O2     ÏàËÆ¶È:57.1%
Journal of Heterocyclic Chemistry          2004          41          915-929
Unexpected formation of 1,2-dihydro-2-azolyl-and azinylisoquinolines by the reduction of the corresponding isoquinolinium salts with sodium borohydride in methanol
Ibolya Prauda,M¨¢ria T¨®th-Lauritz and J¨®zsef Reiter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     compound 6f
    ÏàËÆ¶È:57.1%
Journal of Heterocyclic Chemistry          2010          47          85-90
Regioselective synthesis of pyrimido[5,4-c][2,1]benzothiazines by reactions of ¦Â-chloroaldehydes with n-c-n binucleophiles
Kirill Popov, Tatyana Volovnenko, Alexander Turov and Yulian Volovenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     Compound 7
    ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry Letters          2005          15          3782-3786
Synthesis of novel curcumin mimics with asymmetrical units and their anti-angiogenic activity
Ho Bum Woo, Woon-Seob Shin, Seokjoon Lee, Chan Mug Ahn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     Compound 1c
    ÏàËÆ¶È:57.1%
Magnetic Resonance in Chemistry          2006          44          637-640
1H and 13C spectral assignment of 4-aryl-1, 4, 5, 6, 7, 8-hexahydro-2, 7, 7, 5-oxo-quinolines 3-substituted derivatives (pages 637¨C640)
Esperanza Salfr¨¢n, Margarita Su¨¢rez, Dolores Molero, Roberto Mart¨ªnez-¨¢lvarez, Yamila Verdecia, Estael Ochoa, Amaury Alvarez, Carlos Seoane, Antonio Herrera and Nazario Mart¨ªn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     Octacosylferulate
    ÏàËÆ¶È:57.1%
Journal of China Pharmaceutical University          2003          34          377-379
Stuides on the Chemical Constituents of Euphorbia ebracteolata
FU Guang-Miao; YU Bo-Yang; ZHU Dan-Ni
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     N-{3-[3-(4-hydroxy-3-methoxy-phenyl)-acryloyl]-phenyl}butyramide
C20H21NO4     ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry          2008          16          3608-3615
Synthesis of curcumin mimics with multidrug resistance reversal activities
Yumi Um, Sungsik Cho, Ho Bum Woo, Yong Kee Kim, Hanna Kim, Jungyeob Ham, Su-Nam Kim, Chan Mug Ahn, Seokjoon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     ethyl 3-methyl-1-(4-nitrophenyl)-1H-benzo[f]-chromene-2-carboxylate
    ÏàËÆ¶È:57.1%
Indian Journal of Chemistry          2011          50B          1755-1761
Br§¶nsted acid catalyzed one-pot condensation of ¦Â-naphthol, aldehyde and active methylene substrate: Synthesis of naphthopyrans
Srihari, P; Ganganna, B; Rajendraprasad, K; Bhunia, Dinesh C; Yadav, J S
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     2-{(Z)-1-cyano-2-[4-nitrophenyl]etenyl]}-4-methyl-3-quinolinecarboxylic acid,ethyl ester
C22H17N3O4     ÏàËÆ¶È:57.1%
Journal of Heterocyclic Chemistry          2011          48          1149-1153
Synthesis of heterocyclic derivatives of alkyl 2-(cyanomethyl)-4-methyl-3-quinolinecarboxylates
Alexey S. Degtyarenko, Andrey A. Tolmachev and Yulian M. Volovenko
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     3-methyl-2¦Î,4E-decadienyl (2,3-dimethylphenoxy)acetate
C21H30O3     ÏàËÆ¶È:57.1%
Russian Journal of Organic Chemistry          2001          37          246-255
Synthesis of Analogs of Juvenile Hormons Proceeding from Phenol Derivatives
E.T. Yamansarova, A.G. Kukovinets, O.S. Kukovinets, R.A. Zainullin and F.Z. Galin, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     3-methyl-2¦Î,4E-decadienyl (2,4-dichlorophenoxy)acetate
C19H24Cl2O3     ÏàËÆ¶È:57.1%
Russian Journal of Organic Chemistry          2001          37          246-255
Synthesis of Analogs of Juvenile Hormons Proceeding from Phenol Derivatives
E.T. Yamansarova, A.G. Kukovinets, O.S. Kukovinets, R.A. Zainullin and F.Z. Galin, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     compound 12a
    ÏàËÆ¶È:57.1%
Bioorganic & Medicinal Chemistry Letters          2011          21          3573-3577
Synthesis of substituted triazolyl curcumin mimics that inhibit RANKL-induced osteoclastogenesis
Sang-Kyu Park, Sangtae Oh, Hye Kyoung Shin, Seong Hwan Kim, Jungyeob Ham, Jae-Seok Song, Seokjoon Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (2S,3S)-2,3-bis[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-1,4-butanediol 1,4-diferulate
C42H46O14     ÏàËÆ¶È:57.1%
Journal of Natural Medicines          2011          65          198-201
Chemical constituents of the stems and twigs of Lindera umbellata
Minpei Kuroda ,Koichiro Sakurai ,Yoshihiro Mimaki
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     hycandinic acid ester-1
C21H28O9     ÏàËÆ¶È:56.5%
Journal of Natural Products          1998          61          1187-1193
Antitubercular Natural Products: Berberine from the Roots of Commercial Hydrastis canadensis Powder. Isolation of Inactive 8-Oxotetrahydrothalifendine, Canadine, ¦Â-Hydrastine, and Two New Quinic Acid Esters, Hycandinic Acid Esters-1 and -2
Elmer J. Gentry, Hanuman B. Jampani, Ali Keshavarz-Shokri, Martha D. Morton, David Vander Velde, Hanumaiah Telikepalli, and Lester A. Mitscher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     hycandinic acid ester-2
C21H28O9     ÏàËÆ¶È:56.5%
Journal of Natural Products          1998          61          1187-1193
Antitubercular Natural Products: Berberine from the Roots of Commercial Hydrastis canadensis Powder. Isolation of Inactive 8-Oxotetrahydrothalifendine, Canadine, ¦Â-Hydrastine, and Two New Quinic Acid Esters, Hycandinic Acid Esters-1 and -2
Elmer J. Gentry, Hanuman B. Jampani, Ali Keshavarz-Shokri, Martha D. Morton, David Vander Velde, Hanumaiah Telikepalli, and Lester A. Mitscher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     6-butoxycarbonyl-2'-hydroxy-6'-hydroxymethyl-2,3,3',4,4'-pentamethoxy-1,1'-biphenyl
C23H30O9     ÏàËÆ¶È:56.5%
Heterocycles          2009          77          1409-1416
Preparation of 5H,7H-Dibenz[c,e]oxepin-5-one Derivative through Reconstruction of the Lactone Ring
Hitoshi Abe, Masatsugu Arai, Yasuo Takeuchi, and Takashi Harayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     isoindoloisoquinoline
C26H23NO4     ÏàËÆ¶È:56.5%
Tetrahedron Letters          2004          45          1253-1256
Tandem Parham cyclisation--¦Á-amidoalkylation reaction in the synthesis of the isoindolo[1,2-a]isoquinoline skeleton of nuevamine-type alkaloids
I?aki Osante, Esther Lete, Nuria Sotomayor
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     compound 10d
C24H24N2O5     ÏàËÆ¶È:56.5%
Tetrahedron          2012          68          2864-2875
Synthesis of benzoindoloquinolizines via a Cu(I)-mediated C¨CN bond formation
Rattana Worayuthakarn, Prattya Nealmongkol, Somsak Ruchirawat, Nopporn Thasana
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     E-ferulic acid hexacosyl ester
    ÏàËÆ¶È:54.5%
China Journal of Chinese Materia Medica          2003          28          946-948
Phenolic Compounds Isolated from Rhizoma of Aster tataricus
WNAG Guoyan, WU Tao, LIN Pingchuan, CHOU Guixin, WANG Zhentao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     10-(4-methoxyphenylamino)-2,4-dimethyl-1,5-diazabenzo-fluoren-11-one
C24H19N3O2     ÏàËÆ¶È:54.5%
Journal of Heterocyclic Chemistry          2000          37          241-244
Synthesis of azaindenoquinoline analogs of amsacrine
R. Barret, S. Ortillon, M. Mulamba, J. Y. Laronze, J. L¨¦vy and C. Trentesaux
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     compound 4b
C58H81N3O6     ÏàËÆ¶È:54.5%
Tetrahedron Letters          2002          43          6249-6253
New type chiral calix[4](aza)crowns: synthesis and chiral recognition
Yongbing He, Yuanjing Xiao, Lingzhi Meng, Zhenya Zeng, Xiaojun Wu, Cheng-Tai Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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1
1 .     sinapaldehyde
    ÏàËÆ¶È:72.7%
China Journal of Chinese Materia Medica          2008          33          1453-1461
Studies on Chemical Constituents of Daphne holosericea (Diels) Hamaya
CHEN Yuqi, SU Juan, SHEN Yunheng, ZHANG Wei, HU Xiaojia, XU Wenzheng, ZHANG Weidong, KONG Lingyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     sinapapldehyde
C11H12O4     ÏàËÆ¶È:72.7%
Acta Pharmaceutica Sinica          1999          Vol 34          203-206
CHEMICAL CONSTITUENTS FROM MICHELIA SPHAERANTHA C.Y.WU
Lin Jia (Lin J); Hao Xiaojiang (Hao XJ) and Liang Guangyi (Liang GY)
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     sinapaldehyde
    ÏàËÆ¶È:72.7%
China Journal of Chinese Materia Medica          2011          Vol 36,Issue 8          1019-1023
Study on chem ical constituents from ethyl acetate extract ofMyricaria bracteata
ZHANG Ying, YUAN Yi, CUI Baosong, LI Shuai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     sinapaldehyde
C11H12O4     ÏàËÆ¶È:72.7%
Chinese Journal of Natural Medicines          2005          3          228-230
Constituents of the Barks of Fraxinus chinensis Roxb.
WEI Xiu-Li; YANG Chun-Hua; LIANG Jing-Yuª¬
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     sinapaldehyde
    ÏàËÆ¶È:72.7%
Chinese Pharmaceutical Journal          2008          43          1453-1456
Studies on Chemical Constituents of Daphne holosericea (Diels) Hamaya
CHEN Yu-qi, SU Juan, SHEN Yun-heng, ZHANG Wei, HU Xiao-jia, XU Wen-zheng, ZHANG Wei-dong, KONG Ling-yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     sinapaldehyde
    ÏàËÆ¶È:63.6%
China Journal of Chinese Materia Medica          2010          35          3161-3164
Chemical constituents of Swertia macrosperma
WANG Hongling; GENG Chang¡äan; ZHANG Xuemei; MA Yunbao; JIANG Zhiyong; CHEN Jijun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ferulyl aldehyde
    ÏàËÆ¶È:54.5%
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
8 .     coniferaldehyde
C10H10O3     ÏàËÆ¶È:54.5%
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
9 .     3-(4-Hydroxy-3-methoxyphenyl)-propenal
    ÏàËÆ¶È:54.5%
Chemistry of Natural Compounds          2012          48          168-169
CHEMICAL CONSTITUENTS OF Eria spicata
Liqin Wang,Mingmei Wu,Jian Huang,Jihua Wang,Yegao Chen,and Benlin Yin1
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     coniferyl aldehyde
C10H10O3     ÏàËÆ¶È:54.5%
Chinese Traditional and Herbal Drugs          2006          37          652-655
Phenolic components from Dendrobium nobile
ZHANG Xue; GAO Hao; WANG Nai-li; YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     coniferyl aldehyde
    ÏàËÆ¶È:54.5%
Chinese Journal of Natural Medicines          2007          5          193-196
Chemical Constituents from Inula cappa
XIE Hong-Gang; ZHANG Hong-Wu; ZHANG Jiang; XU Li-Zhen; ZOU Zhong-Mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     Coniferaldehyde
    ÏàËÆ¶È:54.5%
Chinese Journal of Natural Medicines          2008          6          116-119
Chemical Constituents of Clematis montana
SONG Cheng-Zhi; WANG Yue-Hu; HUA Yan; WU Zhang-Kang; DU Zhi-Zhi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     3'-Methoxy-4'-hydroxy-trans-cinnamaldehyde
    ÏàËÆ¶È:54.5%
Archives of Pharmacal Research          2001          24          194-197
Phytochemical constituents of Artemisia japonica ssp. Littoricola
Hak Cheol Kwon and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     3'-Methoxy-4'-hydroxy-trans-cinnamaldehyde
C10H10O3     ÏàËÆ¶È:54.5%
Archives of Pharmacal Research          2001          24          312-315
Phytochemical constituents of Artemisia stolonifera
Hak Cheol Kwon, Sang Un Choi and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3-¼×Ñõ»ù-4ôÇ»ù-¹ðƤȩ
C10H10O3     ÏàËÆ¶È:54.5%
Chinese Journal of Medicinal Chemistry          2005          15          103-107
Studies on the chemical constituents of Bulbophyllum odoratissimum Lindl.
LIU Dai-lin, PANG Fa-gen, ZHANG Jia-xin, WANG Nai-li, YAO Xin-sheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Coniferaldehyde
C10H10O3     ÏàËÆ¶È:54.5%
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
17 .     1-benzyl-5-tert-butyl-3-methylpyrazole
    ÏàËÆ¶È:54.5%
Heterocycles          2001          55          331-352
Scope and Limitations in the Regioselective Synthesis of 1,3,5-Trisubstituted Pyrazoles from ¦Â-Amino Enones and Hydrazine Derivatives. 13C-Chemical Shift Prediction Rules for 1,3,5-Trisubstituted Pyrazoles
Angel Alberola, Luis Calvo Bleye, Alfonso Gonz¨¢lez-Ortega,* M. Luisa S¨¢daba, and M. Carmen Sa?udo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     1-tert-butyl-5-methyl-3-phenylpyrazole
C14H18N2     ÏàËÆ¶È:54.5%
Heterocycles          2001          55          331-352
Scope and Limitations in the Regioselective Synthesis of 1,3,5-Trisubstituted Pyrazoles from ¦Â-Amino Enones and Hydrazine Derivatives. 13C-Chemical Shift Prediction Rules for 1,3,5-Trisubstituted Pyrazoles
Angel Alberola, Luis Calvo Bleye, Alfonso Gonz¨¢lez-Ortega,* M. Luisa S¨¢daba, and M. Carmen Sa?udo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     tert-butyl 3-amino-4-methylphenylcarbamate
    ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry          2010          18          292-304
Application of a novel [3+2] cycloaddition reaction to prepare substituted imidazoles and their use in the design of potent DFG-out allosteric B-Raf inhibitors
Justin Dietrich, Vijay Gokhale, Xiadong Wang, Laurence H. Hurley, Gary A. Flynn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     ferulaldehyde
C10H10O3     ÏàËÆ¶È:54.5%
Natural Product Research and Development          2009          21          733-736
Chemical Constituents from the Aerial Parts of Daphne bholua
CHEN Hu-hai;ZHANG Wei-dong;SU Juan; CHEN Yu-qi; SHEN Yun-heng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     coniferaldehyde
    ÏàËÆ¶È:54.5%
Chinese Traditional and Herbal Drugs          2011          42          244-246
Chemical constituents in fruit of Melia azedarach (II)
CHONG Xiao-tao, SHI Yan-peng, CHENG Zhan-li, YAO Qing-qiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     2-(Bromomethyl)-1,4-dimethoxynaphthalene
C13H13BrO2     ÏàËÆ¶È:53.8%
Chemical & Pharmaceutical Bulletin          2011          59(3)          302-314
Preparations of Anthraquinone and Naphthoquinone Derivatives and Their Cytotoxic Effects
Xing-Ri CUI,Ryota SAITO, Takatsugu KUBO, Daijiro KON,Yuich HIRANO,and Setsuo SAITO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     SF2738D
C13H11N3OS     ÏàËÆ¶È:53.8%
The Journal of Antibiotics          1994          47          1385-1394
NOVEL ANTIBIOTICS SF2738A, B AND C, AND THEIR ANALOGS PRODUCED BY Streptomyces sp.
SHUICHI GOMI, SHOICHI AMANO, ERIKO SATO, SHINJI MIYADOH, YOSHIO KODAMA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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3
1 .     ent-4(15)-eudesmene-1¦Â,6¦Á-diol
C15H26O2     ÏàËÆ¶È:75%
Phytochemistry          2005          66          1662-1670
ent-Verticillane-type diterpenoids from the Japanese liverwort Jackiella javanica
Fumihiro Nagashima , Katsuhiro Kishi, Yuko Hamada,Shigeru Takaoka, Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     4(15)-eudesmene-1¦Â,6¦Á-diol
C15H24O     ÏàËÆ¶È:75%
Phytochemistry          2003          64          303-323
Terpenoids from the seeds of Artemisia annua
Geoffrey D. Brown, Guang-Yi Liang, Lai-King Sy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     4(15)-eudesmene-1¦Â,6¦Á-diol
C15H26O2     ÏàËÆ¶È:75%
Phytochemistry          2002          59          811-815
Sesquiterpenoids of Torilis japonica fruit
Junichi Kitajima, Nobuyuki Suzuki, Mituru Satoh, Mitsuo Watanabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     4(15)-eudesmene-1¦Â,6¦Á-diol
C15H26O2     ÏàËÆ¶È:75%
Journal of Natural Products          2004          67          1975-1979
Four New Eudesmanes from Caragana intermedia and Their Biological Activities
Zhihua Sun, Bo Chen, Su Zhang, and Changqi Hu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     eudesm-4(15)-ene-1¦Â,6Rdiol
C15H26O2     ÏàËÆ¶È:75%
Journal of Natural Products          2003          66          609-615
New Sesquiterpenes from Litsea verticillata
Hong-Jie Zhang, Ghee Teng Tan, Bernard D. Santarsiero, Andrew D. Mesecar, Nguyen Van Hung, Nguyen Manh Cuong, D. Doel Soejarto, John M. Pezzuto, and Harry H. S. Fong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     voleneol
    ÏàËÆ¶È:75%
Acta Botanica Yunnanica          2001          23(4)          521-526
Chemical Constituents of Calophyllum polyanthum
CHEN Ji-Jun,XU Min,LUO Shi- De,WANG Hui-Ying,XU Jian- Chu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     1¦Â,6¦Á-dihydroxyeudesm-4(15)-ene
C15H26O2     ÏàËÆ¶È:75%
Chemical & Pharmaceutical Bulletin          1987          35          2272-2279
Studies on the Sesquiterpenes from Ambrosia elatior LINN¨¦
TAICHI OHMOTO,KEIJI IKEDA,SACHIYO NOMURA,MASARU SHIMIZU and SACHI SAITO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     polydactin B
C15H26O2     ÏàËÆ¶È:75%
Journal of Asian Natural Products Research          2008          10          277-280
Two new sesquiterpenoids from the soft coral Sinularia polydactyla (Ehreberg)
Cui-Xian Zhang, Chen-Chen Zhu, Su-Jun Yan, Jun Li, Jing-Yu Su, Yong-Ju Liang, Xiao-Ping Yang,Kang-Cheng Zheng and Long-Mei Zeng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     eudesm-4(15)-ene-1¦Â,6¦Á-diol
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          2009          34          1101-1103
Chemical constituents from air-dried Piper longum
LIU Wenfeng, JIANG Zhiyong, CHEN Jijun, ZHANG Xuemei, MA Yunbao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     4(15)-eudesmene-1¦Â,6¦Á-diol
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          2009          34          2758-2760
Chemical constituents from Aeschynanthus longicaullis
CHEN Lin, KANG Wenyi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     1¦Â,6¦Á-dihydroxyeudesmane-4(14)-ene
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          2005          30          1595-1597
Study on the chemical constituents in herb of Hypericum attenuatum
DONG Jianyong, JIA Zhongjian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     1¦Â,6¦Á-dihydroxy-4(14)-eudesmene
    ÏàËÆ¶È:75%
China Journal of Chinese Materia Medica          2002          27          40-42
Lipid Compounds from Echinacea purpurea
Lii Jiren, GAO Xiufen AI Tie min ZHAO Yuying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     1¦Â,6¦Á-dihydroxy-4(14)-eudesmene
    ÏàËÆ¶È:75%
Phytochemistry          1996          43          815-817
Eudesmane sesquiterpenes from Artemisia eriopoda
Jin-Feng Hu, Su-Ping Bai, Zhong-Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     1¦Á-hydroxyeudesmane
    ÏàËÆ¶È:75%
Journal of Natural Products          1995          Vol 58          428-431
7-epi-Eudesmanes from Teucrium polium
Alaa Kamel
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     4(15)-Eudesmene-1¦Â,6¦Á-diol
    ÏàËÆ¶È:75%
Phytochemistry          1995          39          603-607
Sesquiterpenes from leaves of Cryptomeria japonica
Wen-Chiung Su, Jim-Min Fang, Yu-Shia Cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     Eudesma-4(14)-ene-1¦Â,6¦Á-diol
C15H26O2     ÏàËÆ¶È:75%
Phytochemistry          1994          36          119-127
Terpenoids of Alisma orientale rhizome and the crude drug alismatis rhizoma
Yoshijiro Nakajima, Yohko Satoh, Masumi Katsumata (nee Ohtsuka), Kazuko Tsujiyama (nee Mikoshiba), Yoshiteru Ida, Junzo Shoji
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     1¦Â,6¦Á-¶þôÇ»ùèñÍé-4(15)-Ï© [1¦Â,6¦Á-dihydroxyeudesm-4(15)-ene]
C15H24O2     ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2011          42(4)          664-667
Chemical constituents of Dracocephalum heterophyllum and antibacterial activity
REN Ai-mei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     1¦Â,6¦Á-dihydroxy-4(15)-eudesmene
    ÏàËÆ¶È:75%
Phytochemistry          1988          27          2225-2228
Guaianolides and other constituents of Helianthus microcephalus
Alicia B. Gutierrez,Werner Herz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     1¦Â,6¦Á-dihydroxyeudesm-4(15)-ene
    ÏàËÆ¶È:75%
Phytochemistry          1988          27          3664-3667
Components from Santolina rosmarinifolia,subspecies rosmarinifolia and canescens
M.P. Maqua,A.C.G. Vines,E. Caballero,M.C. Grande,M. Medarde,I.S. Bellido
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     1¦Â,6¦Á-dihydroxyeudesm-4(15)-ene
C15H26O2     ÏàËÆ¶È:75%
Chinese Traditional and Herbal Drugs          2010          41          1608-1612
Chemical constituents in Senecio vulgaris
LIU Yong-heng; ZHANG Zi-ping; WANG Yong-li
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     1¦Â,6¦Á-Dihydroxy-4(15)-eudesmene
    ÏàËÆ¶È:75%
Archives of Pharmacal Research          2001          24          194-197
Phytochemical constituents of Artemisia japonica ssp. Littoricola
Hak Cheol Kwon and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     1¦Â,6¦Á-Dihydroxy-4(15)-eudesmene
    ÏàËÆ¶È:75%
Archives of Pharmacal Research          2004          27          1016-1019
A new sesquiterpene lactone from Artemisia rubripes nakai
Kyu Ha Lee, Yong Deuk Min, Sang Zin Choi, Hak Cheol Kwon and Ock Ryun Cho, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     4(15)-Eudesmene-1¦Â,6¦Á-diol
    ÏàËÆ¶È:75%
Archives of Pharmacal Research          2007          30          1067-1074
Lignan and terpene constituents from the aerial parts of saussurea pulchella
Sang Un Choi, Min Cheol Yang, Kyu Ha Lee, Ki Hyun Kim and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     1¦Â,6¦Á-dihydroxy-4(15)-eudesmene
    ÏàËÆ¶È:75%
Journal of Chemical Research          2010          34          425-427
A new sesquiterpenoid eremophilenolactone from Senecio nemorensis
Zhao, Ruijian; Xie, Weidong; Liu, Yuxue; Meng, Fanjun; Zhao, Hong; Lai, Pengxiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     1¦Â,6¦Á-Dihydroxy-4(14)-eudesmene
    ÏàËÆ¶È:75%
Fitoterapia          2011          82          225-229
A new natural spiro heterocyclic compound and the cytotoxic activity of the secondary metabolites from Juniperus brevifolia leaves
Laila M. Moujir, Ana M.L. Seca, Liliana Araujo, Artur M.S. Silva, M. Carmo Barreto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     ent-4(15)-eudesmene-1¦Â,6¦Á-diol
    ÏàËÆ¶È:75%
Chinese Journal of Natural Medicines          2012          10          36-39
Chemical constituents of Allophylus longipes
Xiang-Yun ZHANG, Xiang-Hai CAI, Xiao-Dong LUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     1¦Â-O-¦Â-D-glucopyranosy-6¦Á-hydroxyeudesman-4(15)-ene
C21H36O7     ÏàËÆ¶È:71.4%
Planta Medica          2005          71          268-272
New Sesquiterpenes from Erigeron annus
Li, Xin; Yang, Min; Han, Yi-Feng; Gao, Kun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     1¦Â,6¦Á-Dihydroxyeudesm-4(15)-ene
C15H26O2,     ÏàËÆ¶È:70%
Phytochemistry          1995          39          1127-1131
Sesquiterpene lactones and other constituents from Hymenoxys richardsonii and H. subintegra
Ahmed A. Ahmed, O. Spring, Mohamed H. Abd El-Razek, Nadia S. Hussein, Tom J. Mabry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     4(15)-eudesmene-1¦Â,6¦Á-diol
    ÏàËÆ¶È:70%
Journal of the Chinese Chemical Society          2005          52          369-374
Terpenoids from the Flower of Cacalia tangutica
Xia Liu, Quan-Xiang Wu and Yan-Ping Shi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     Leptocladolin A
C17H28O3     ÏàËÆ¶È:65%
Bulletin of the Chemical Society of Japan          2010          83          678-682
Oppositane-Type Sesquiterpenoids from the Formosan Soft Coral Sinularia leptoclados
Chiung-Yao Huang, Jui-Hsin Su, Yung-Chun Liu, Zhi-Hong Wen, Chi-Hsin Hsu, Michael Y. Chiang, Jyh-Horng Sheu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     (7R*)-opposit-4(15)-ene-7-acetoxy-1¦Â-ol
C17H28O3     ÏàËÆ¶È:65%
Chemistry & Biodiversity          2011          8          643-650
Antiproliferative Compounds of Cyphostemma greveana from a Madagascar Dry Forest
Shugeng Cao, Yanpeng Hou, Peggy Brodie, James S. Miller, Richard Randrianaivo, Etienne Rakotobe, Vincent E. Rasamison and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     compound 2a
    ÏàËÆ¶È:60%
Chemical & Pharmaceutical Bulletin          1987          35          2272-2279
Studies on the Sesquiterpenes from Ambrosia elatior LINN¨¦
TAICHI OHMOTO,KEIJI IKEDA,SACHIYO NOMURA,MASARU SHIMIZU and SACHI SAITO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     ammolactone-A
    ÏàËÆ¶È:60%
Phytochemistry          1997          44          907-910
Ammolactone, a guaianolide from a medicinal plant, Ammodaucus leucotrichus
Bernard Muckensturm, Fouzia Diyani, Didier Le Nou?n, Souad Fkih-Tetouani, Jean-Pierre Reduron
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     1¦Á-acetoxyl ent-junenol
C17H28O3     ÏàËÆ¶È:60%
Chinese Traditional and Herbal Drugs          2003          34          487-489
A new ent-eudesmane-type sesquiterpene from leaves of Polyalthia cheliensis
ZHU Wei-ming; NING Xian-jiang; KANG Wen-yi; HAO Xiao-jiang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     7¦Ä-Methoxy-4(14)-oppositen-1¦Â-ol
    ÏàËÆ¶È:60%
Archives of Pharmacal Research          2007          30          1067-1074
Lignan and terpene constituents from the aerial parts of saussurea pulchella
Sang Un Choi, Min Cheol Yang, Kyu Ha Lee, Ki Hyun Kim and Kang Ro Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     (1R*,2R*,4aS*,5S*,8aR*)-Decahydro-5-hydroxy-4a-methyl-2-(1-methylethyl)-8-methylidenenaphthalen-1-yl Acetate
C17H29O3     ÏàËÆ¶È:60%
Chemistry & Biodiversity          2011          8          643-650
Antiproliferative Compounds of Cyphostemma greveana from a Madagascar Dry Forest
Shugeng Cao, Yanpeng Hou, Peggy Brodie, James S. Miller, Richard Randrianaivo, Etienne Rakotobe, Vincent E. Rasamison and David G. I. Kingston
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     3-oxo-9¦Â-hydroxy-deoxyandrographolide
C20H28O5     ÏàËÆ¶È:60%
Natural Product Communications          2011          6          781-784
Microbial Transformation of Deoxyandrographolide by Alternaria alternata AS 3.4578
Xiu-Lan Xin, Sha Deng, Bao-Jing Zhang, Shan-shan Huang, Yan Tian, Xiao-Chi Ma, *, Lei An, Xiao-hong Shu, Ji-Hong Yao and Xun Cui*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     24-propyl-5¦Á-cholesta-3¦Â,5,6¦Â,8,15¦Á,28,29-heptaol
C30H54O7     ÏàËÆ¶È:56%
Russian Chemical Bulletin          1994          43          1726-1730
Polyhydroxysteroids from the Far-Eastern starfishCtenodiscus crispatus
A. A. Kicha, A. I. Kalinovskii, N. I. Ivanchina, Yu. N. El'kin and V. A. Stonik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     3¦Á,4¦Á-dihydroxyclerodan-15-oic acid
C20H36O4     ÏàËÆ¶È:55%
Helvetica Chimica Acta          2003          Vol. 86          3187
Dinorditerpene, Diterpenes, Alkaloids, and Coumarins from Clausena dunniana
Hong-Ping He, Yue-Mao Shen, Guo-Ying Zuo, Xiao-Sheng Yang, and Xiao-Jiang Hao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     elongatol C
C15H24O3     ÏàËÆ¶È:55%
Chemical & Pharmaceutical Bulletin          2007          55(5)          762-765
Nardosinane Sesquiterpenoids from the Formosan Soft Coral Nephthea elongata
Shang-Kwei WANGa and Chang-Yih DUH
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     ent-1¦Á-18-dihydroxy-6-oxo-13-epi-manoyl oxide
C20H32O4     ÏàËÆ¶È:55%
Phytochemistry          2006          67          2294-2302
Biotransformations of ent-18-acetoxy-6-ketomanoyl oxides epimers at C-13 with filamentous fungi
Hanae Ghoumari, Mohamed-Hassan Benajiba, Andr¨¦s Garc¨ªa-Granados,Antonia Fern¨¢ndez, Antonio Mart¨ªnez, Francisco Rivas, Jos¨¦ M. Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     15-bromoparguer-9(11)-ene-16-ol
C20H31BrO     ÏàËÆ¶È:55%
Phytochemistry          2004          65          2527-2532
Halogenated diterpenoids from the red alga Laurencia nipponica
Ekaterina G. Lyakhova, Anatoly I. Kalinovsky, Sophia A. Kolesnikova,Victor E. Vaskovsky, Valentin A. Stonik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     4¦Á-eudesmene-1¦Â,6¦Á-diol
C15H26O3     ÏàËÆ¶È:55%
Phytochemistry          2002          59          811-815
Sesquiterpenoids of Torilis japonica fruit
Junichi Kitajima, Nobuyuki Suzuki, Mituru Satoh, Mitsuo Watanabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     1¦Â,6¦Á-Dihydroxy-4¦Â(15)-epoxyeudesmane
C15H26O3     ÏàËÆ¶È:55%
Planta Medica          2005          71          268-272
New Sesquiterpenes from Erigeron annus
Li, Xin; Yang, Min; Han, Yi-Feng; Gao, Kun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     vitetrifolin A
C20H32O3     ÏàËÆ¶È:55%
Phytochemistry          2000          55          873-877
Diterpenoids from the fruits of Vitex trifolia
Masateru Ono, Hiromi Sawamura, Yasuyuki Ito, Koichi Mizuki , Toshihiro Nohara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     compound 2b
    ÏàËÆ¶È:55%
Chemical & Pharmaceutical Bulletin          1987          35          2272-2279
Studies on the Sesquiterpenes from Ambrosia elatior LINN¨¦
TAICHI OHMOTO,KEIJI IKEDA,SACHIYO NOMURA,MASARU SHIMIZU and SACHI SAITO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     delatisine
C20H25NO3     ÏàËÆ¶È:55%
Chemistry of Natural Compounds          2000          36          419-477
HETISANE-TYPE DITERPENOID ALKALOIDS
I. A. Bessonova and Sh. A. Saidkhodzhaeva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     15-bromoparguer-9(11)-en-16-ol
    ÏàËÆ¶È:55%
Molecules          2008          13          2894-2899
Halogenated Terpenes and a C15-Acetogenin from the Marine Red Alga Laurencia saitoi
Nai-Yun Ji, Xiao-Ming Li and Bin-Gui Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     7¦Á-dihydroxy-24-nor-5¦Â-cholane-23-phosphonicacid
    ÏàËÆ¶È:55%
Steroids          2005          70          681-689
Synthesis and in vitro cholesterol dissolution by 23- and 24-phosphonobile acids
Ponnusamy Babu, Uday Maitra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     (-)-3¦Á,4¦Â-dihydroxykolavelool
    ÏàËÆ¶È:55%
Phytochemistry          1999          50          455-461
Rearranged (4¡ú2)-abeo-clerodane and clerodane diterpenes from Aristolochia chamissonis
Mauro D. Bomm, J. Zukerman-Schpector , Lucia M. X. Lopes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     3¦Á,4¦Â-Dihydroxy-15,16-epoxy-12-oxo-cleroda-13(16),14-diene
    ÏàËÆ¶È:55%
Phytochemistry          1996          41          561-563
Clerodane diterpenes and other constituents of Croton hovarum
Hans C. Krebs, Harisolo Ramiarantsoa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     Clerod-14-ene-3¦Á,4¦Â,13¦Î-triol
    ÏàËÆ¶È:55%
Phytochemistry          1996          41          499-502
Terpenoid constituents of Viguiera tucumanensis
Karina M. Meragelman, Luis Ariza Espinar, Virginia E. Sosa, Mar¨ªa L. Uriburu, Juana R. de la Fuente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     12¦Á-hydroxy-13-epi-manoyloxide
C24H34O2     ÏàËÆ¶È:55%
Phytochemistry          1995          40          1201-1207
Diterpenoids from Grindelia tarapacana
Lin Zhou, Eduardo R. Fuentes, Joseph J. Hoffmann, Barbara N. Timmerman
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