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1 .     tetrahydrohelenalin
    ÏàËÆ¶È:66.6%
Magnetic Resonance in Chemistry          1987          25          201-202
Carbon-13 NMR spectra of some pseudoguaianolides
Guillermo Delgado, Laura Alvarez, Eduardo Huerta, Alfonso Romo de Vivar and Rachel Mata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     3¦Á,4¦Á-epoxy-5¦ÁH,7¦ÁH,6¦ÂH,11¦ÂH-eudesman-6,12-olide
    ÏàËÆ¶È:60%
Journal of Natural Products          1993          Vol 56          1723
A Short Synthesis of (+)-Colartin and (+)-Arbusculin A from (-)-Santonin
Gonzalo Blay, Luz Cardona, Begoña Garcia, Jose R. Pedro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     3¦Â,8¦Á-dihydroxy-4¦Â,5¦Á,11¦Â-H-eudesman-6¦Á,12-olide
C15H24O4     ÏàËÆ¶È:60%
Journal of Natural Products          1995          Vol 58          1498-1507
Microbial Transformations of 6¦Á- and 6 ¦Â-Eudesmanolides by Rhizopus nigricans Cultures
Yolanda Garc¨ªa, Andr¨¦s Garc¨ªa-Granados, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     3¦Â,9¦Á-diacetoxycedran-8¦Á-ol
C19H30O5     ÏàËÆ¶È:60%
Phytochemistry          1995          39          1081-1084
The biotransformation of 8-epicedrol and some relatives by Cephalosporium aphidicola
Estelle Gand, James R. Hanson, Habib Nasir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     Jasonone
C12H20O2     ÏàËÆ¶È:60%
Zeitschrift f¨¹r Naturforschung B          2007          62b          125-128
Jasonone, a Nor-sesquiterepene from Jasonia montana
Abou El-Hamd H. Mohamed
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     11,12-Dihydroxydrimene-15-oic acid
C15H24O4     ÏàËÆ¶È:60%
Journal of Asian Natural Products Research          2013          15          305-309
Two new sesquiterpenes from cultures of the basidiomycete Agaricus arvensis
Jiang-Yuan Zhao, Jian-Hai Ding, Zheng-Hui Li, Ze-Jun Dong, Tao Feng, Hong-Bin Zhang & Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     1-tert-Butyl 3-methyl (3S,5R)-5-[(1,1-dimethyl-2-oxoethyl) amino]piperidine-1,3-dicarboxylate
C16H28N2O5     ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2013          21          5907-5922
Synthesis and optimization of novel (3S,5R)-5-(2,2-dimethyl-5-oxo-4-phenylpiperazin-1-yl)piperidine-3-carboxamides as orally active renin inhibitors
Yutaka Mori, Yasuyuki Ogawa, Akiyoshi Mochizuki, Yuji Nakamura, Teppei Fujimoto, Chie Sugita, Shojiro Miyazaki, Kazuhiko Tamaki, Takahiro Nagayama, Yoko Nagai, Shin-ichi Inoue, Katsuyoshi Chiba, Takahide Nishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     methyl longipin-9-en-15-oate
C16H24O3     ÏàËÆ¶È:56.2%
Journal of Natural Products          1994          Vol 57          873
¦Á-Longipinene Derivatives from Santolina viscosa. A Conformational Analysis of the Cycloheptane Ring
A. F. Barrero, M. M. Herrador, J. Molina Molina, J. F. Qu¨ªlez, M. Quir¨®s
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     methyl 12-hydroxylongipin-9-en-15-oate
    ÏàËÆ¶È:56.2%
Journal of Natural Products          1994          Vol 57          873
¦Á-Longipinene Derivatives from Santolina viscosa. A Conformational Analysis of the Cycloheptane Ring
A. F. Barrero, M. M. Herrador, J. Molina Molina, J. F. Qu¨ªlez, M. Quir¨®s
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     compound 6
    ÏàËÆ¶È:56.2%
Journal of Natural Products          1994          Vol 57          873
¦Á-Longipinene Derivatives from Santolina viscosa. A Conformational Analysis of the Cycloheptane Ring
A. F. Barrero, M. M. Herrador, J. Molina Molina, J. F. Qu¨ªlez, M. Quir¨®s
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 10
    ÏàËÆ¶È:56.2%
Tetrahedron          2011          67          8348-8352
The total synthesis of (-)-connatusin A, a hirsutane-type sesquiterpene isolated from the fungus Lentinus connatus BCC8996
David J.-Y. D. Bon, Martin G. Banwell , Ian A. Cade, Anthony C. Willis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     compound 7a
    ÏàËÆ¶È:56.2%
Indian Journal of Chemistry Section B          1985          24B          1208-1214
Proton & Carbon-13 NMR Studies of trans-Clerodane Diterpenoids & Congeners:Stereochemical Implications & Certain Correlations with cis-Clerodanes
A S SARMA & A K GAYEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 4c
C18H23NO2     ÏàËÆ¶È:56.2%
Chinese Journal of Organic Chemistry          2013          33          2196-2204
Synthesis and Antibacterial Activity of New Pinanyl Nitrogen-Containing Heterocycles
Wei Baisong, Gu Wen, Xu Xu, Yang Yiqin, Wang Shifa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ent-16,17,19-trihydroxygibberell-20-oic acid 20,19-lactone
C20H30O4     ÏàËÆ¶È:55%
Phytochemistry          1993          34          693-696
Bio-transformation of gibberellin 20,19-lactones by Rhizopus stolonifer
Braulio M. Fraga, J.Clemente Diaz Gomez, M.Shaiq Ali, James R. Hanson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     dendronobilin I
C15H24O3     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2007          Vol. 90          2386
Nine New Sesquiterpenes from Dendrobium nobile
Xue Zhanga)b)c), Hong-Wei Liud), Hao Gaoa)b)c), Hui-Ying Hane), Nai-Li Wangb)e), Hou-Ming Wuf), Xin-Sheng Yaoe), and Zhao Wang
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 25
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2003          66          344-349
Chemical Transformations on Botryane Skeleton. Effect on the Cytotoxic Activity
Jos L. Reino, Rosa Durn-Patrn, Inmaculada Segura, Rosario Hernndez-Galn, Hans H. Riese, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     3,4-epoxy-11¦Á,13-dihydroelemen-12, 8-olide
C15H22O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          2001          64          466-471
Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla
Bao-Ning Su,Yoshihisa Takaishi, Tetsuya Yabuuchi, Takenori Kusumi, Motoo Tori,Shigeru Takaoka,Gisho Honda, Michiho Ito, Yoshio Takeda, Olimjon K. Kodzhimatov, and Ozodbek Ashurmetov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     8-bromo-3-isopropyl-6-methyltricyclo-[4.4.0.02,8]dec-3-ene-7-one
    ÏàËÆ¶È:53.3%
Journal of Natural Products          2001          64          406-410
A Formal Total Synthesis of Racemic Sesquiterpenoid Sativene
Sasan Karimi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     compound 12
C15H18O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          22-30
Guaianolides as Immunomodulators. Synthesis and Biological Activities of Dehydrocostus Lactone, Mokko Lactone, Eremanthin, and Their Derivatives
Saori Yuuya, Hisahiro Hagiwara, Toshio Suzuki, Masayoshi Ando, Atsushi Yamada, Kouji Suda, Takao Kataoka, and Kazuo Nagai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (4R,5R,8R)-4,5-epoxycaryophyllan-8-ol
C14H23O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          41-44
Biotransformation of Caryophyllene Oxide by Botrytis cinerea
Rosa Duran, Elena Corrales, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     epidihydropseudoivalin
C15H22O3     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          920-922
Oxidative Transformations of Guaia-1(10)-en-12, 8-olides into Xanthanolides
Mariano Mart¨ªnez-V¨¢zquez, Jorge C¨¢rdenas, Lucas Godoy, Martha Mart¨ªnez-Bahena, Ren¨¦ Miranda, and Manuel Salm¨®n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     1¦Â-hydroxy-4¦Á,11¦ÁH-eudesma-5-en-12,8¦Â-olide
C15H22O3     ÏàËÆ¶È:53.3%
Planta Medica          2003          69          662-666
Sesquiterpenes and Other Constituents from the Aerial Parts of Inula japonica
Chao Yang,Chun-Ming Wang,Zhong-Jian Jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     ¦Â-cyclocostunolide
C15H20O2     ÏàËÆ¶È:53.3%
Acta Botanica Yunnanica          1997          19(1)          85-91
STUDY ON CHEMICAL CONSTITUENTS OF SAUSSUREA LAPPA
Yang Hui,¡¡Xie Jinlun, ¡¡Sun Handong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
24 .     sulfoorientalol b
C15H26O5S     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          1994          42          2430-2435
Crude Drugs from Aquatic Plants. V. On the Constituents of Alismatis Rhizoma. (3). Stereostructures of Water-Soluble Bioactive Sesquiterpenes, Sulfoorientalols a, b, c, and d, from Chinese Alismatis Rhizoma
Masayuki YOSHIKAWA,Shoko YAMAGUCHI,Hisashi MATSUDA,Nobumitsu TANAKA,Johji YAMAHARA and Nobutoshi MURAKAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     sulfoorientalol b
C15H26O5S     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          1993          41          1194-1196
SULFOORIENTALOLS a, b, c, AND d, FOUR NEW BIOLOGICALLY ACTIVE SESQUITERPENES, FROM ALISMATIS RHIZOMA
Masayuki YOSHIKAWA,Youich FUKUDA,Shoko HATAKEYAMA,Nobumitsu TANAKA,Hisashi MATSUDA,Johji YAMAHARA and Nobutoshi MURAKAMI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     1,5,5,9-Tetramethylspir0[3.5]nonan-l-ol
C13H24O     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          1980          63          154-190
Photochemische Reaktionen. 106. Mitteilung. Zur Photochemie tetraalkylsubstituierter ¦Ã-Keto-olefine
Jacob Berger, Michikazu Yoshioka, Markus P. Zink, Hans R. Wolf, Oskar Jeger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
27 .     (1S,2S,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-yl-ethanal
    ÏàËÆ¶È:53.3%
Molecules          2009          14          2780-2800
Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol®
Laura Chapado, Pablo J. Linares-Palomino, Concepci¨®n Bad¨ªa, Sof¨ªa Salido, Manuel Nogueras, Adolfo S¨¢nchez and Joaqu¨ªn Altarejos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
28 .     Kobusone
C14H22O2     ÏàËÆ¶È:53.3%
Biochemical Systematics and Ecology          2007          35          470-471
Kobusone: Occurrence of a norsesquiterpenoid in the gorgonian coral Rumphella antipathies (Gorgoniidae)
Li-Fan Chuang, Tung-Yung Fan, Jan-Jung Li, Ping-Jyun Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
29 .     3¦Á,11¦Â-dihydroxy-1,2,4¦Â,5¦Á,6¦Â-H-eudesman-6,12-olide
C15H24O4     ÏàËÆ¶È:53.3%
Natural Product Research          2008          22          499-506
Biotransformation of tetrahydro-¦Á-santonins by Absidia coerulea
Lin Yang; Jungui Dai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
30 .     diversifolide
C13H20O3     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          1999          47          428-429
A New Dinorxanthane and Chromone from the Root of Tithonia diversifolia
Yueh-Hsiung KUO and Ben-Yan LIN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
31 .     1¦Á-hydroxycolartin or 1¦Á,4¦Á-dihydroxyeudesman-5¦Á,6¦Â,7¦Á,11bH-12,6-olide
C15H24O4     ÏàËÆ¶È:53.3%
Phytochemistry          1999          51          995-997
Minor eudesmanolides from Artemisia canariensis
Horacio Mansilla, J. Antonio Palenzuela
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
32 .     5¦Â-hydroxy-4,9-oxidogermacr-11¦Á-H,13-6,12-olide
C15H24O4     ÏàËÆ¶È:53.3%
Phytochemistry          1994          37          1211-1212
A germacranolide from Cyathocline lutea
S.R. Rojatkar, M. Banerjee, D.D. Sawaikar, B.A. Nagasampagi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
33 .     5,5,9-Èý¼×»ù-1-ôǼ׻ùÂÝ[5.5]-8-ʮһϩ-3-ͪ(b)
    ÏàËÆ¶È:53.3%
Chemical Journal of Chinese Universities          2003          24          1820-1824
Total Synthesis of (¡À)-¦Á-Chamigrene-3-one
WANG Jin-Jun, YIN Jun-Gang, WU Xu-Ran, ZHAO Yan,TAKESHITA Histoshi, MORIA kira, HATSUI Toshihide
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
34 .     compound 49
C14H20O     ÏàËÆ¶È:53.3%
Canadian Journal of Chemistry          2006          84          1456-1469
Intramolecular [4 + 3] cycloadditions -Stereochemical issues in the cycloaddition reactions of cyclopentenyl cations - A synthesis of (+)-dactylol1
Michael Harmata, Paitoon Rashatasakhon, and Charles L. Barnes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
35 .     hydroxyenone
    ÏàËÆ¶È:53.3%
Organic Letters          2003          Vol. 5, No. 13          2295-2298
Enantiospecific First Total Synthesis and Assignment of Absolute Configuration of the Sesquiterpene (-)-Cucumin H
A. Srikrishna and Dattatraya H. Dethe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
36 .     1-Methyl-2-{[(1R,2R,5R)-6,6-dimethylbicyclo[3.1.1]heptyl-2]methylsulfonyl}-1H-imidazole
C14H22N2O2S     ÏàËÆ¶È:53.3%
Chemistry of Natural Compounds          2012          48          38-42
SYNTHESIS OF NEW MONOTERPENE SULFONYLIMIDAZOLES
M. Ya. Demakova,D. V. Sudarikov,S. A. Rubtsova,L. L. Frolova,and A. V. Kuchin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
37 .     3-keto-drimenol
C15H24O2     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2009          57          433-435
Sesquiterpenes from Cultures of the Basidiomycete Clitocybe conglobata and Their 11¦Â-Hydroxysteroid Dehydrogenase Inhibitory Activity
Di Xu, Yu Sheng, Zhong-Yu Zhou, Rong Liu, Ying Leng and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
38 .     3-keto-drimenol
C15H24N2     ÏàËÆ¶È:53.3%
Chemical & Pharmaceutical Bulletin          2009          57          433-435
Sesquiterpenes from Cultures of the Basidiomycete Clitocybe conglobata and Their 11¦Â-Hydroxysteroid Dehydrogenase Inhibitory Activity
Di Xu, Yu Sheng, Zhong-Yu Zhou, Rong Liu, Ying Leng and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
39 .     neopulchellin
    ÏàËÆ¶È:53.3%
Phytochemistry          1988          27          2887-2891
Sesquiterpene lactones from Gaillardia pulchella
Sanggong Yu,Nianbai Fang,Tom J. Mabry,Khalil A. Abboud,Stanley H. Simonsen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
40 .     compound 7
    ÏàËÆ¶È:53.3%
Phytochemistry          1990          29          977-979
Oplopanes from the leaves of Senecio mexicanus
Pedro Joseph-Nathan,J.Roberto Villag¨®mez,Luisa U. Rom¨¢n,Juan D. Hern¨¢ndez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
41 .     11¦Â,13-dihydrosantamarin 3,4¦Á-epoxyde
C15H22O4     ÏàËÆ¶È:53.3%
Phytochemistry          1990          29          2913-2917
Sesquiterpene lactones from Artemisia caerulescens Subsp. gargantae
Juan F. Sanzand,J.Alberto Marco
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
42 .     tannunolide C
    ÏàËÆ¶È:53.3%
Phytochemistry          1990          29          3575-3580
Guaianolides from Tanacetum annuum
Alejandro F. Barrero,Juan F. S¨¢nchez,Jos¨¦ Molina,Antonio Barr¨®n,M del Mar Salas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
43 .     Cosmosoic Acid
C15H22O3     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2010          93          753-756
Two Novel 15(10¡ú1)Abeomuurolane Sesquiterpenes from Cosmos sulphureus
Jyh-Horng Wu, Yi-Fu Chang, Yu-Tang Tung, Minoru Tsuzuki, Akira Izuka, Sheng-Yang Wang and Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
44 .     Cosmosaldehyde
C15H22O2     ÏàËÆ¶È:53.3%
Helvetica Chimica Acta          2010          93          753-756
Two Novel 15(10¡ú1)Abeomuurolane Sesquiterpenes from Cosmos sulphureus
Jyh-Horng Wu, Yi-Fu Chang, Yu-Tang Tung, Minoru Tsuzuki, Akira Izuka, Sheng-Yang Wang and Yueh-Hsiung Kuo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
45 .     2¦Â-hydroxy-( + )-prezizane
    ÏàËÆ¶È:53.3%
Phytochemistry          1981          20          1597-1599
Jinkohol, a prezizane sesquiterpene alcohol from agarwood
Tsutomu Nakanishi, Etsuko Yamagata, Kaisuke Yoneda, Iwao Miura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
46 .     eremoligularin
C15H22O4     ÏàËÆ¶È:53.3%
Tetrahedron Letters          2004          45          8855-8858
Bieremoligularolide and eremoligularin, two novel sesquiterpenoids from Ligularia muliensis
Qiu-Hong Wu, Chun-Ming Wang, Sheng-Gao Cheng, Kun Gao
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
47 .     (1R,6R,7R,10S)-6-Hydroxy-7-(1-methylethyl)-10-methylbicyclo[4.4.0]decan-4-one
C14H24O2     ÏàËÆ¶È:53.3%
Journal of the Chemical Society, Perkin Transactions 1          2000                   189-194
Synthesis of sesquiterpene allylic alcohols and sesquiterpene dienes from Cupressus bakeri and Chamaecyparis obtusa
Koon-Sin Ngo and Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
48 .     jinkohol
    ÏàËÆ¶È:53.3%
Journal of the Chemical Society, Perkin Transactions 1          1983                   601-604
Jinkoh-eremol and jinkohol II, two new sesquiterpene alcohols from agarwood
Tsutomu Nakanishi, Etsuko Yamagata, Kaisuke Yoneda, Iwao Miura and Hideo Mori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
49 .     10¦ÂH,11¦ÁH-7¦Á-Hydroxy-8-oxoeremophilan-12,6-olide
C15H22O4     ÏàËÆ¶È:53.3%
Tetrahedron          2008          64          9136-9142
Isolation of new eremophilane-type sesquiterpenoids, subspicatins A¨CD and subspicatolide from Ligularia subspicata, and chemical and genetic diversity of the species
Motoo Tori, Yasuko Okamoto, Kana Tachikawa, Kanako Mihara, Aki Watanabe, Misato Sakaoku, Shigeru Takaoka, Masami Tanaka, Xun Gong, Chiaki Kuroda, Masato Hattori, Ryo Hanai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
50 .     compound 25
C15H20O5I     ÏàËÆ¶È:53.3%
The Journal of Organic Chemistry          2002          67          5461-5469
Synthesis of (+)-8-Deoxyvernolepin and Its 11,13-Dihydroderivative. A Novel Reaction Initiated by Sulfene Elimination Leads to the 2-Oxa-cis-decalin Skeleton
Alejandro F. Barrero, J. Enrique Oltra, M¨ªriam ¨¢lvarez, and Antonio Rosales
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
51 .     (1R,7S,8S)-7-hydroxy-1,4,4,8-tetramethyltricyclo[6.3.0.02,6]undec-2(6)-en-3-one,
C15H22O2     ÏàËÆ¶È:53.3%
Indian Journal of Chemistry Section B          2011          50B          1092-1106
Enantiospecific first total synthesis of cucumin-H
Srikrishna, A; Dethe, Dattatraya H
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
52 .     (2aR,4aR,5R,7aR,7bS)-5-hydroxy-2,2,4a-tri-methyldecahydrocyclobuta[e]indene-7a-carbaldehyde
C15H24O2     ÏàËÆ¶È:53.3%
Russian Journal of Organic Chemistry          2004          40          1441-1449
Transformations of caryophyllene diepoxides in various acidic media
O. V. Salomatina, D. V. Korchagina, Yu. V. Gatilov, M. P. Polovinka and V. A. Barkhash
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
53 .     agripilolactone
C15H24O3     ÏàËÆ¶È:53.3%
Journal of Chemical Research          2011          35          116-118
A new sesquiterpenoid from a Fusarium spp. an endophytic fungus in Agriminia pilosa
Wang, Jian-Wei; Li, Cheng-Ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
54 .     (3aS,5aR,6R,7R,8R,9S,9aS,9bS)-6,7,8,9-diepoxy-5a,9-dimethyl-3-methylidene-5. 3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-2-one
C15H18O4     ÏàËÆ¶È:53.3%
Phytochemistry          2012          80          70-76
Sesquiterpenes from the leaves of Laurus nobilis L.
Elin Julianti, Kyoung Hwa Jang, Sooryun Lee, Dongha Lee, Woongchon Mar, Ki-Bong Oh, Jongheon Shin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
55 .     (-)-(3R)-3-hydroxy-isolongifolol
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Oleo Science          2010          59          243-246
Microbial Transformation of (-)-Isolongifolol by Plant Pathogenic Fungus Glomerella cingulata
Mitsuo Miyazawa, Kazuki Sakata, Masashi Ueda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
56 .     ¦Â-cyclocostunolide
    ÏàËÆ¶È:53.3%
Phytochemistry          2013          95          19-93
Sesquiterpenoids in subtribe Centaureinae (Cass.) Dumort (tribe Cardueae, Asteraceae): Distribution, 13C NMR spectral data and biological properties Review Article
Maurizio Bruno, Svetlana Bancheva, Sergio Rosselli, Antonella Maggio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
57 .     gomerolactone D
C15H21ClO3     ÏàËÆ¶È:53.3%
European Journal of Organic Chemistry          2009          2009          1407-1411
Novel Lactone Chamigrene-Derived Metabolites from Laurencia majuscula
Ana R. D¨ªaz-Marrero, Inmaculada Brito, Jos¨¦ M. de la Rosa, Luis D'Croz, Oscar Fabelo, Catalina Ruiz-P¨¦rez, Jos¨¦ Darias and Mercedes Cueto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
58 .     1,7-dimethyltricyclo[6.2.2.0(4,9)]dodec-6-en-3-one
C14H20O     ÏàËÆ¶È:53.3%
European Journal of Organic Chemistry          2006          2006          3181-3192
Towards the Total Synthesis of Vibsanin E, 15-O-Methylcyclovibsanin B,3-Hydroxyvibsanin E, Furanovibsanin A, and 3-O-Methylfuranovibsanin A
Brett D. Schwartz, David P. Tilly, Ralf Heim, Stefan Wiedemann, Craig M. Williams and Paul V. Bernhardt
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
59 .     jinkohol
    ÏàËÆ¶È:53.3%
Flavour and Fragrance Journal          2000          15          61-83
1,7-Cyclogermacra-1(10),4-dien-15-al, a sesquiterpene with a novel skeleton, and other sesquiterpenes from Haitian vetiver oil
Peter Weyerstahl, Helga Marschall, Ute Splittgerber and Dietmar Wolf
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
60 .     (-)-10-oxo-isodauc-3-en-15-oic acid
C15H22O3     ÏàËÆ¶È:53.3%
Journal of Natural Medicines          2012          66          453-458
Pyrenes and pyrendiones from Uvaria lucida
Masataka Moriyasu, Sousuke Takeuchi, Momoyo Ichimaru, Noriyshi Nakatani and Yumi Nishiyama, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
61 .     eremoligularin
    ÏàËÆ¶È:53.3%
Chinese Traditional and Herbal Drugs          2012          43          1270-1272
Chemical constituents of Ligularia intermedia from Henan Province
YUAN Yong-liang; YE Dan-dan; LIANG Hui-juan; LIU Wei; BAI Su-ping
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
62 .     ¦Â-cyclocostunolide
    ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2012          37          1232-1236
Chemical constituents from a portion of ethanolicextract of Saussurea lappa roots
ZHANG Ting; MA Lin; WU Feng; CHEN Ruoyun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
63 .     ¦Â-cyclocostunolide
    ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2012          37          1249-1253
Chemical constituents of Dolomiaea souliei
WEI Hua; HE Chunnian; PENG Yong; MA Guoxu; XIAO Peigen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
64 .     kobusone
    ÏàËÆ¶È:53.3%
China Journal of Chinese Materia Medica          2012          37          1973-1976
Sesquiterpenes and monoterpene from Aquilaria sinensis
YANG Lin; QIAO Lirui; XIE Dan; DAI Jungui; GUO Shunxing
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
65 .     compound 4a
C17H21NO2     ÏàËÆ¶È:53.3%
Chinese Journal of Organic Chemistry          2013          33          2196-2204
Synthesis and Antibacterial Activity of New Pinanyl Nitrogen-Containing Heterocycles
Wei Baisong, Gu Wen, Xu Xu, Yang Yiqin, Wang Shifa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
66 .     compound 4b
C17H20NO2Cl     ÏàËÆ¶È:53.3%
Chinese Journal of Organic Chemistry          2013          33          2196-2204
Synthesis and Antibacterial Activity of New Pinanyl Nitrogen-Containing Heterocycles
Wei Baisong, Gu Wen, Xu Xu, Yang Yiqin, Wang Shifa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
67 .     compound 25
    ÏàËÆ¶È:53.3%
Magnetic Resonance in Chemistry          1987          25          619-627
Structural studies in the cedrane series by 13C NMR
P. Brun, J. Casanova, Muppala S. Raju, B. Waegell, Ernest Wenkert and J. P. Zahra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
68 .     compound 26
    ÏàËÆ¶È:53.3%
Magnetic Resonance in Chemistry          1987          25          619-627
Structural studies in the cedrane series by 13C NMR
P. Brun, J. Casanova, Muppala S. Raju, B. Waegell, Ernest Wenkert and J. P. Zahra
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
69 .     lycopodatine A
C17H28NO2     ÏàËÆ¶È:52.9%
Journal of Natural Products          2005          68          1809-1812
Lycopodatines A−C, C16N Alkaloids from Lycopodium inundatum
Hiroshi Morita, Yusuke Hirasawa, and Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
70 .     11¦Á,13-dihgdrochamissonolide
    ÏàËÆ¶È:52.9%
Planta Medica          1995          61          544-550
Sesquiterpene Lactones and Inositol Esters from Arnica angustfolial
Thomas J. Schmidt, G¨¹nter Willuhn. Alois Steigel, andDetlefWendisch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
71 .     11¦Á,13-dihydro-6-deoxychamissonolide
    ÏàËÆ¶È:52.9%
Planta Medica          1995          61          544-550
Sesquiterpene Lactones and Inositol Esters from Arnica angustfolial
Thomas J. Schmidt, G¨¹nter Willuhn. Alois Steigel, andDetlefWendisch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
72 .     turberostemoninol
C22H29NO6     ÏàËÆ¶È:52.9%
Chinese Chemical Letters          1993          4          1067-1070
TWO MINOR ALKLOIDS FROM THE ROOTS OF STEMONA TUBEROSA
WEN HAN LIN,LEI WANG LIANG QIAO,MENG SHEN CAI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
73 .     10-epi-Dihydrobotrydial
C17H28O5     ÏàËÆ¶È:52.9%
Phytochemistry          1996          41          513-517
Biologically active sesquiterpenoid metabolites from the fungus Botrytis cinerea
Isidro G. Collado, Rosario Hern¨¢ndez-Gal¨¢n, Victoria Prieto, James R. Hanson, Laureana G. Rebordinos
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
74 .     stcmominoamide
C17H23NO4     ÏàËÆ¶È:52.9%
Phytochemistry          1994          36          1333-1335
Two minor alkaloids from roots of Stemona tuberosa
Wen Han Lin, Li Ma, Meng Shen Cai, Roderick A. Barnes
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
75 .     4-O-acetyl-11¦ÁH,13-dihydrorudmollin
C17H26O5     ÏàËÆ¶È:52.9%
Phytochemistry          1992          31          2051-2054
Sesquiterpene lactones and other constituents from Rudbeckia mollis
Marta Vasquez, Leovigildo Quijano, Lowell E. Urbatsch, Nikolaus H. Fischer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
76 .     lycopodatines A
C17H27NO2     ÏàËÆ¶È:52.9%
Heterocycles          2009          77          679-729
The Lycopodium Alkaloids
Yusuke Hirasawa, Jun'ichi Kobayashi, and Hiroshi Morita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
77 .     2¦Á-Acetoxy-11¦Á,l3-dihydroconfertin
C15H22O4     ÏàËÆ¶È:52.9%
Phytochemistry          1985          24          1017-1019
Pseudoguaianolides related to confertin from Stevia isomeca
Ferdinand Bohlmann, Kazuyasu Umemoto, Jasmin Jakupovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
78 .     lycoflexine
    ÏàËÆ¶È:52.9%
Tetrahedron Letters          2002          43          8307-8311
Seven new Lycopodium alkaloids, lycoposerramines-C, -D, -E, -P, -Q, -S, and -U, from Lycopodium serratum Thunb.
Hiromitsu Takayama, Kazuaki Katakawa, Mariko Kitajima, Kentaro Yamaguchi, Norio Aimi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
79 .     (1S,8R,9S)-9-isopropyl-8-(methoxymethoxy)-1-methylbicyclo[6.3.0]undec-5-en-3-ol
C17H30O3     ÏàËÆ¶È:52.9%
Indian Journal of Chemistry Section B          2011          50B          73-76
Enantiospecific approach to AB-ring system of the diterpenes fusicoccanes
Srikrishna, A; Nagaraju, Gopalasetty
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
80 .     compound 13
    ÏàËÆ¶È:52.6%
Steroids          1992          57          306-312
Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17¦Á-methyl steroids: synthesis and rearrangement
Honggang Bi, Robert Mass¨¦, George Just
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
81 .     oxandrolone
    ÏàËÆ¶È:52.6%
Steroids          1992          57          537-550
17-Epimerization of 17¦Á-methyl anabolic steroids in humans: metabolism and synthesis of 17¦Á-hydroxy-17¦Â-methyl steroids
Willi Schänzer, Georg Opfermann, Manfred Donike
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
82 .     decarboxywedeligenin
    ÏàËÆ¶È:52.6%
Organic Magnetic Resonance          1982          18          138-142
13C NMR spectra of wedeloside and related kaurenoid derivatives
I. A. S. Lewis and J. K. MacLeod
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
83 .     ( R,1- S,3¦ÁR,4S,8¦ÁS,9S)- Decahydro- ,4,8,8-tetramethyl-1,4-methanoazulene-9-methanol
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          2003          Vol. 86          106
The Ozonolysis of Longifolene: A Tool for the Preparation of Useful Chiral Compounds. Configuration Determination of New StereogenicCenters by NMR Spectroscopy and X-Ray Crystallography
Vladimir Dimitrov, Gudrun Hopp Rentsch, Anthony Linden, and Manfred Hesse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
84 .     (S,1S,3¦ÁR,4S,8¦ÁS,9S)-Decahydro- ,4,8,8-tetramethyl-1,4-methanoazulene-9-methanol
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          2003          Vol. 86          106
The Ozonolysis of Longifolene: A Tool for the Preparation of Useful Chiral Compounds. Configuration Determination of New StereogenicCenters by NMR Spectroscopy and X-Ray Crystallography
Vladimir Dimitrov, Gudrun Hopp Rentsch, Anthony Linden, and Manfred Hesse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
85 .     1¦Á,3¦Â-dihydroxyambrox
C16H28O3     ÏàËÆ¶È:50%
Journal of Natural Products          2006          69(6)          957-959
Biotransformation of (−-Ambrox by Cell Suspension Cultures of Actinidia deliciosa
Asma Nasib, Syed Ghulam Musharraf, Sajjad Hussain, Saifullah Khan,Shazia Anjum, Shamsher Ali, Atta-ur-Rahman, and M. Iqbal Choudhary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
86 .     compound 2a
C18H34O4     ÏàËÆ¶È:50%
Journal of Natural Products          2007          70          575-583
Megastigmanes and Their Glucosides from the Whole Plant of Sedum sarmentosum
Masayuki Yoshikawa,Toshio Morikawa, Yi Zhang,Seikou Nakamura, Osamu Muraoka, and Hisashi Matsuda
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
87 .     serratine
C16H25NO3     ÏàËÆ¶È:50%
Journal of Natural Products          2007          70          1024-1028
Fawcettimine-Related Alkaloids from Lycopodium serratum
Kazuaki Katakawa,Akiko Nozoe,Noriyuki Kogure, Mariko Kitajima,Masakiyo Hosokawa, and Hiromitsu Takayama
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
88 .     4¦Á-acetyl-guaia-1(10)-en-13¦Á-methyl-12,8¦Â-olide
C17H24O4     ÏàËÆ¶È:50%
Journal of Natural Products          1999          62          920-922
Oxidative Transformations of Guaia-1(10)-en-12, 8-olides into Xanthanolides
Mariano Mart¨ªnez-V¨¢zquez, Jorge C¨¢rdenas, Lucas Godoy, Martha Mart¨ªnez-Bahena, Ren¨¦ Miranda, and Manuel Salm¨®n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
89 .     2¦Â-hydroxy-8,15(R)-oxydo-ent-pimaran
C20H34O3     ÏàËÆ¶È:50%
Chemical & Pharmaceutical Bulletin          1983          31          4409-4416
Chemische und Chemotaxonomische Untersuchungen der Pterophyten. XLIV. Chemische Untersuchungen der Inhaltsstoffe von Microlepia marginata (PANZER) C. CHR. (2)
TADAYUKI KURAISHI,TAKAO TANIGUCHI,KAZUYUKI HORI,TAKAO MURAKAMI,NOBUTOSHI TANAKA,YASUHISA SAIKI and CHIUMING CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
90 .     abbeokutone
    ÏàËÆ¶È:50%
China Journal of Chinese Materia Medica          2008          33          1566-1568
Studies on chemical constituents from stem bark of Trwia nudiflora
WU Shaohua, SHENG Yuemao, CHEN Youwei, YANG Liyuan, LI Shaolan, LI Zhiying
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
91 .     ¦Á-hydroxy-10¦Á-methoxyguaian-12,6-olide
C16H26O4     ÏàËÆ¶È:50%
Phytochemistry          1998          49          559-564
Antimycobacterial evaluation of germacranolides in honour of professor G.H. Neil Towers 75th birthday
Nikolaus H. Fischer, Tiansheng Lu, Charles L. Cantrell, Jos¨¦ Castañeda-Acost¦Á, Leovigildo Quijano, Scott G. Franzblau
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
92 .     compound 13
    ÏàËÆ¶È:50%
Journal of Natural Products          1984          Vol 47          592-599
Cmr Spectroscopy of Labdanic Diterpenes and Related Substances
Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
93 .     methyl 4-(2-hydroxy-1,5-dimethyl-3-oxohexyl)-1-cyclo-hexene-1-carboxylate
C16H26O4     ÏàËÆ¶È:50%
Phytochemistry          1993          32          1163-1165
Juvabione analogues from two Abies sachalinensis trees
Kenzo Kawai, Chika Takahashi, Tamie Takada, Atsushi Numata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
94 .     4¦Â,10¦Â-dihydroxy-1¦Á-methoxy-5¦Á,11¦ÁH-guaia-2-en-12,6¦Á-olide
C16H24O5     ÏàËÆ¶È:50%
Phytochemistry          1992          31          863-880
Sesquiterpene lactones and other constituents from Ursinia species
J. Jakupovic, U. Ganzer, P. Pritschow, L. Lehmann, F. Bohlmann, R.M. King
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
95 .     compound 4
    ÏàËÆ¶È:50%
Phytochemistry          1991          30          4177-4179
A triterpenoid glucoside from Barringtonia acutangula
Bikas C. Pal, Basudeb Achari, Keith R. Price
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
96 .     methyl 4-[2,3,3-trimethyl-6,9-dithiaspiro[4.4]-non-2-yl]-4-pentenoate
C16H26O2S2     ÏàËÆ¶È:50%
Indian Journal of Chemistry Section B          2007          46B          805-817
Total synthesis of (¡À)-¦Â-microbiotene,(¡À)-microbiotol,(¡À)-cyclocuparanol and (¡À)-¦Â-cuparenones
Srikrishna,A; Ramachary,D B
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
97 .     Longibornyl acetate
    ÏàËÆ¶È:50%
Phytochemistry          1985          24          2893-2898
Foliage sesquiterpenes of Dacrydium cupressinum: identification, variation and biosynthesis
Katherine M. Berry, Nigel B. Perry, Rex T. Weavers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
98 .     compound Ia
    ÏàËÆ¶È:50%
Steroids          1983          41          493-500
Metabolism of 17¦Á-methyl-5¦Â-dihydrotestosterone in the rabbit
John F. Templeton, Chung-Ja Choi Jackson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
99 .     compound VIIa
    ÏàËÆ¶È:50%
Steroids          1983          41          493-500
Metabolism of 17¦Á-methyl-5¦Â-dihydrotestosterone in the rabbit
John F. Templeton, Chung-Ja Choi Jackson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
100 .     compound 14
    ÏàËÆ¶È:50%
Tetrahedron Letters          2001          42          5617-5620
Free radical reactions for heterocycle synthesis. Part 5: Formation of novel bridged spirolactones by double cyclizations
Wei Zhang, Georgia Pugh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
101 .     compound 24a
C16H24O4     ÏàËÆ¶È:50%
Tetrahedron Letters          2004          45          383-386
Carbanion cyclisation of esters. Part 2: Enantiospecific construction of the tricyclic framework of the marine sesquiterpenes, spirodysins
A. Srikrishna, P. Ravi Kumar, S.S.V. Ramasastry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
102 .     Isopimara-7,15-dien-1¦Â,19-diol
C20H32O2     ÏàËÆ¶È:50%
Tetrahedron          2012          68          819-829
Potential anti-inflammatory diterpenes from Premna obtusifolia
Abdul-Wahab Salae, Apinya Rodjun, Chatchanok Karalai, Chanita Ponglimanont, Suchada Chantrapromma, Akkharawit Kanjana-Opas, Supinya Tewtrakul, Hoong-Kun Fun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
103 .     (R)-ethyl-5-((1R,3aR,7aR)-7a-methyl-4-oxo-octahydro-1H-inden-1-yl)hexanoate
    ÏàËÆ¶È:50%
Bioorganic & Medicinal Chemistry          2010          18          4119-4137
Vitamin D receptor agonist/histone deacetylase inhibitor molecular hybrids
Marc Lamblin, Basel Dabbas, Russell Spingarn, Rodrigo Mendoza-Sanchez, Tian-Tian Wang, Beum-Soo An, Dao Chao Huang, Richard Kremer, John H. White, James L. Gleason
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
104 .     Cermizine D
C16H30N2     ÏàËÆ¶È:50%
Tetrahedron          2004          60          7015-7023
New phlegmarane-type, cernuane-type, and quinolizidine alkaloids from two species of Lycopodium
Hiroshi Morita, Yusuke Hirasawa, Takakazu Shinzato, Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
105 .     3¦Á,17-dihydroxyspongia-13(16),14-dien-2-one
C20H28O4     ÏàËÆ¶È:50%
Tetrahedron          1994          50          9893-9908
Scalemic 12-hydroxyambliofuran and 12-acetoxy-ambliofuran, five tetracyclic furanoditerpenes and a furanosesterterpene from Spongia sp.
Philip A. Searle, Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
106 .     (1S,5R,8S,10S,11R)-10-(methoxymethoxy)-8,10,11-trimethyltricyclo[6.3.0.01,5]undecan-4-one
C16H26O3     ÏàËÆ¶È:50%
Tetrahedron          2012          68          2650-2656
Enantiospecific first total synthesis of (6S,7R)-silphiperfolan-6-ol
A. Srikrishna, Gopalasetty Nagaraju, Vishal M. Sheth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
107 .     O-methyldihydrobotrydial
C18H30O5     ÏàËÆ¶È:50%
Agricultural and Biological Chemistry          1988          52          1845-1847
Isolation and Structures of O-Methyldihydrobotrydial and Deacetyl-O-methyldihydrobotrydialone Produced by Botrytis squamosa
Yasuo KIMURA, Hiroaki FUJIOKA, Hiromitsu NAKAJIMA, Takashi HAMASAKI, Akira ISOGAI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
108 .     (1S*,2S*,3R*,6R*,7S*,9R*)-(-)-2-thiocyanatoneopupukeanane
C16H25NS     ÏàËÆ¶È:50%
Australian Journal of Chemistry          1997          50          1123-1127
Terpene Metabolites from the Tropical Marine Sponge Axinyssa sp. nov.
Jamie S. Simpson,, Mary J. Garson,, John N. A. Hooper,, Edith I. Cline and Cindy K. Angerhofer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
109 .     (8a¦Â,12a¦Â,13a¦Á)-5,8,8a,9,10,11,12,12a,13,13a-decahydro-8-oxo-6H-isoquino[2,1-g][1,6]naphthyridine
C16H20N2O     ÏàËÆ¶È:50%
Journal of Medicinal Chemistry          1991          34          705-717
Structure-affinity relationships of 12-sulfonyl derivatives of 5,8,8a,9,10,11,12,12a,13,13a-decahydro-6H-isoquino[2,1-g][1,6]naphthyridines at .alpha.-adrenoceptors
Robin D. Clark, David B. Repke, Jacob Berger, Janis T. Nelson, Andrew T. Kilpatrick, Christine M. Brown, Alison C. MacKinnon, Ruth U. Clague, Michael Spedding
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
110 .     compound 12
C16H24O3     ÏàËÆ¶È:50%
Tetrahedron          2013          69          1363-1368
From toluene to triquinanes: formal total syntheses of the sesquiterpenoid natural products (−-hypnophilin and (−-coriolin
David J.-Y.D. Bon, Martin G. Banwell, Jas S. Ward, Anthony C. Willis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
111 .     compound 8
C18H32O4     ÏàËÆ¶È:50%
European Journal of Organic Chemistry          2005          2005          5077-5083
Antimalarial Polyketide Cycloperoxides from the Marine SpongePlakortis simplex
Claudio Campagnuolo, Ernesto Fattorusso, Adriana Romano, Orazio Taglialatela-Scafati, Nicoletta Basilico, Silvia Parapini and Donatella Taramelli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
112 .     compound 35
    ÏàËÆ¶È:50%
Canadian Journal of Chemistry          1979          57          1550-1556
13C nuclear magnetic resonance studies. 85. 13C spectra of several ring-contracted and -expanded steroids
Vinod Dave, J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
113 .     compound 38
    ÏàËÆ¶È:50%
Canadian Journal of Chemistry          1979          57          1550-1556
13C nuclear magnetic resonance studies. 85. 13C spectra of several ring-contracted and -expanded steroids
Vinod Dave, J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
114 .     compound 48
    ÏàËÆ¶È:50%
Canadian Journal of Chemistry          1979          57          1550-1556
13C nuclear magnetic resonance studies. 85. 13C spectra of several ring-contracted and -expanded steroids
Vinod Dave, J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
115 .     compound 49a
    ÏàËÆ¶È:50%
Canadian Journal of Chemistry          1979          57          1550-1556
13C nuclear magnetic resonance studies. 85. 13C spectra of several ring-contracted and -expanded steroids
Vinod Dave, J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
116 .     compound 10b
    ÏàËÆ¶È:50%
Chemistry-A European Journal          2006          12          6572-6584
Asymmetric Total Syntheses of Marine Cyclic Depsipeptide Halipeptins A¨CD
Shouyun Yu, Xianhua Pan and Dawei Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
117 .     (+)-2-[(1S,2R,4aS,8aS)-decahydro-2,5,5,8a-tetramethylnaphthalen-1-yl]oxirane
    ÏàËÆ¶È:50%
Helvetica Chimica Acta          2014          97          197-214
Enantioselective Access to (−-Ambrox® Starting from ¦Â-Farnesene
Christian Chapuis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
118 .     compound 6-Me
C16H24O3     ÏàËÆ¶È:50%
Journal of Natural Medicines          2012          66          453-458
Pyrenes and pyrendiones from Uvaria lucida
Masataka Moriyasu, Sousuke Takeuchi, Momoyo Ichimaru, Noriyshi Nakatani and Yumi Nishiyama, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
119 .     rhodomollein F
C20H32O6     ÏàËÆ¶È:50%
Journal of Asian Natural Products Research          2012          14          764-768
Two new grayanane diterpenoids from the flowers of Rhododendron molle
Zhi-Run Zhang, Jin-Dong Zhong, Hong-Mei Li, Hai-Zhou Li, Rong-Tao Li & Xu-Liang Deng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
120 .     (16R)-16,17-Dihydroxy-ent-kaur-2-one
C20H32O3     ÏàËÆ¶È:50%
Chemistry of Natural Compounds          2013          48          999-1001
A new ent-kaurane diterpenoid from Rubus corchorifolius
Yang-Wen Ou, Xue-Xiang Chen, Min Zhang, Xiao-Juan Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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