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lztadxu

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lztadxu: ½ð±Ò+10, 3q 2012-07-04 08:20:50
leecius: ½ð±Ò+1, лл²ÎÓ룡 2012-07-04 09:10:48
1 .     11¦Á-angeloyloxy-1¦Á-hydroxy-3-oxo-6¦ÁH,7¦ÁH,10¦ÁMe-eudesm-4-en-6,12-olide
C20H26O6     ÏàËÆ¶È:61.1%
Phytochemistry          1997          45          1645-1651
Sesquiterpenolides from Melanoselinum decipiens
Guillermo M. Massanet, Francisco M. Guerra, Zacar¨ªas D. Jorge, Carmen Astorga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     11¦Á,13-dihydroalantolactone
C15H22O2     ÏàËÆ¶È:60%
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
3 .     7-drimen-9¦Á,11,12-triol
C15H26O3     ÏàËÆ¶È:60%
Journal of Natural Products          1999          62          1488-1491
Synthesis of 11, 12-Epoxydrim-8, 12-en-11-ol, 11, 12-Diacetoxydrimane, and Warburganal from (-)-Sclareol
A. F. Barrero, M. Cort¨¦s, E. A. Manzaneda, E. Cabrera, R. Chahboun, M. Lara, and A. R. Rivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     compound 10
C15H20O4     ÏàËÆ¶È:60%
Journal of Asian Natural Products Research          2006          8          317-330
Biotransformation of a- and 10b-santonin by fungus and plant cell cultures
L. YANG, J. DAI, J.-I. SAKAI and M. ANDO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 6
C15H24O4     ÏàËÆ¶È:60%
Acta Pharmaceutica Sinica          2005          Vol 40          834-837
Biotransformation of 6¦Â-santonin by Phytolacca acinosa cell suspension cultures
YANG Lin; DAI Jun-gui
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     (3R,3¦ÁR,4¦ÁS,7¦ÁS,8S,9¦ÁS)-3,4¦Á,8-trimethyldecahydroazuleno[6,5-¦Â]furan-2,5-dione
C15H22O3     ÏàËÆ¶È:60%
Natural Product Research and Development          2010          22          736-739
Sesquiterpenoids from Tibetan Folk Drug Pulicaria insignis
HUANG Sheng-zhuo;JIANG Si-ping; ZHU Hua-jie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     9¦Â-hydroxy-3-oxo-6,7¦ÁH,11¦ÂH-eudesm-4-en-6,12-olide
    ÏàËÆ¶È:60%
Tetrahedron          1995          51          5609-5616
Synthesis of 9-oxyfunctionalized eudesmanes from artemisin
Victoria Bargues, Gonzalo Blay, Bego?a Garc¨ªa, Cristina L. Garc¨ªa, Jos¨¦R. Pedro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     compound 7a
    ÏàËÆ¶È:56.2%
Tetrahedron          1995          51          5609-5616
Synthesis of 9-oxyfunctionalized eudesmanes from artemisin
Victoria Bargues, Gonzalo Blay, Bego?a Garc¨ªa, Cristina L. Garc¨ªa, Jos¨¦R. Pedro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (5¦Â ,6¦Á )-6,11-dihydroxyeudesmane
C15H28O2     ÏàËÆ¶È:53.3%
Chemistry & Biodiversity          2006          Vol. 3          337
New Chemical Constituents from the Endophyte Streptomyces Species LR4614 Cultivated on Maytenus hookeri
Pei-Ji Zhao, Guo-Hong Li, and Yue-Mao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     5-epidilatanolide
    ÏàËÆ¶È:53.3%
Phytochemistry          2002          59          205-213
Eremophilanolides and other constituents from the Argentine liverwort Frullania brasiliensis
Alicia Bard¨®n, Graciela Bovi Mitre, Norma Kamiya, Masao Toyota,Yoshinori Asakawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     2R,11-dihydroxy-1(10)-tremulen-5,12-olide
C15H22O4     ÏàËÆ¶È:53.3%
Journal of Natural Products          2008          71(8)          1423-1426
Sesquiterpenes and Aliphatic Diketones from Cultures of the Basidiomycete Conocybe siliginea
Zhong-Yu Zhou, Jian-Guo Tang, Fei Wang, Ze-Jun Dong, and Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     7-drimen-9¦Á,11-diol
C15H26O2     ÏàËÆ¶È:53.3%
Journal of Natural Products          1999          62          1488-1491
Synthesis of 11, 12-Epoxydrim-8, 12-en-11-ol, 11, 12-Diacetoxydrimane, and Warburganal from (-)-Sclareol
A. F. Barrero, M. Cort¨¦s, E. A. Manzaneda, E. Cabrera, R. Chahboun, M. Lara, and A. R. Rivas
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     compound 15
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1997          60          1026-1030
Sesquiterpene Glycosides and Phenylpropanoid Esters from Phonus arborescens (Carthamus arborescens)
Alejandro F. Barrero, Pilar Arteaga, Jos¨¦F. Qu¨ªlez, Ignacio Rodr¨ªguez, and M. Mar Herrador
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     6-hydroperoxy-5,6-dihydro-4,5-dehydro-epi-antheindurolide A
C15H18O6     ÏàËÆ¶È:53.3%
Natural Product Research          2008          22          907-914
Irregular linear sesquiterpene dilactones from Anthemis auriculata Boiss.
Milka Todorova; Jordanka Staneva; Pavleta Denkova; Ljuba Evstatieva
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     compound 3
    ÏàËÆ¶È:53.3%
Phytochemistry          1993          32          460-462
Sesquiterpene lactones from Artemisia species
J. Alberto Marco, Juan F. Sanz, F. Sancenon, A. Rustaiyan, M. Saberi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     seiricardine B
C15H26O2     ÏàËÆ¶È:53.3%
Phytochemistry          1993          33          69-78
Seiricardines B and C, phytotoxic sesquiterpenes from three species of Seiridium pathogenic for cypress
Antonio Evidente, Andrea Motta, Lorenzo Sparapano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     eremophila-9,11-dien-8¦Á-ol
C15H24O     ÏàËÆ¶È:53.3%
Phytochemistry          1992          31          4027-4028
(+)-(4S*,5R*,7S*,8R*)-eremophila-9,11-dien-8¦Á-ol from the liverwort Marsupella emarginata
Leslie J. Harrison, Hans Becker, Joseph D. Connolly, David S. Rycroft
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     armexifolin
    ÏàËÆ¶È:53.3%
Phytochemistry          1984          23          1665-1668
Sesquiterpene lactones of Artemisia mexicana var. Angustifolia
Rachel Mata, Guillermo Delgado, Alfonso Romo de Vivar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     1(R)-hydroxypolygodial
    ÏàËÆ¶È:53.3%
Tetrahedron Letters          2005          46          4061-4063
Enantioselective synthesis of 1(R)-hydroxypolygodial
Carmela Della Monica, Giorgio Della Sala, Deborah D¡¯Urso, Irene Izzo, Aldo Spinella
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     (3aR,5aS,7R,9aR,9bR)-3a,5a,6,7,8,9,9a,9b-octahydro-7,9b-dimethylnuphtho[1,2-c]-furan-1(3H)-one
C14H20O2     ÏàËÆ¶È:53.3%
Journal of the Chemical Society, Perkin Transactions 1          1985                   861-863
Metabolic products of Phomopsis oblonga. Part 1. 3a,5a,6,7,8,9,9a,9b-Octahydro-7,9b-dimethylnaphtho[1,2-c]furan-1(3H)-one (oblongolide)
Michael J. Begley and John Frederick Grove
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     3¦Â,14¦Â,10¦Á-trihydroxy-1¦Â,6¦Á,7¦Â(H)-cadinane
C15H28O3     ÏàËÆ¶È:53.3%
Tetrahedron          2000          56         
Corrigendum to ¡°Jasonol, a Rare Tricyclic Eudesmane Sesquiterpene and Six other New Sesquiterpenoids from Jasonia candicans¡±
Ahmed A Ahmed, Ahmed A Mahmoud
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (5R)-5-isopropyloct-7-en-2-ol
C11H22O     ÏàËÆ¶È:53.3%
Russian Journal of Organic Chemistry          2011          47          1142-1145
Unusual behavior of methylidentriphenylphosphorane in reactions with seven-membered lactols
G. Yu. Ishmuratov, V. A. Vydrina, M. P. Yakovleva, E. F. Valeeva and R. R. Muslukhov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
23 .     1¦Â-acetoxy-3¦Á-hydroxy-4¦Â,,5¦Á,11¦Â-H-eudesman-6¦Á,12-olide
C17H26O5     ÏàËÆ¶È:52.9%
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
24 .     methyl-1¦Â, 10¦Â-epoxy-6¦Á-hydroxy-7(10)-en-8-oxoeremophil-12-oate
C16H22O5     ÏàËÆ¶È:50%
Planta Medica          1997          63          335-338
New Sesquiterpenes from Two Ligularia Species
Hai-Ruo Peng,Yan-Ping Shi, and Zhong-Jian jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
25 .     methyl-1¦Â,10¦Â-epoxy-7(11)-en-6¦Á-hydroxy-8-oxo-ermophil-12-oate
    ÏàËÆ¶È:50%
Chinese Chemical Letters          1995          6          875-876
NEW SESQUITERPENNE FROM LIGULARIA SAGITTA
LI YANG,HAI RUO PENG,ZHONG JIANG JIA
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
26 .     compound 4
C16H26O3     ÏàËÆ¶È:50%
Tetrahedron Letters          2002          43          9019-9022
Stereoselective synthesis of the fully functionalized core fragment of terpentecin
Taotao Ling, Fatima Rivas, Emmanuel A. Theodorakis
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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