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1 .     (6R,9R) 9-hydroxy-4-megastigmen-3-one
C13H22O2     ÏàËÆ¶È:86.6%
Phytochemistry          2004          65          497-505
Structure elucidation and phytotoxicity of C13 nor-isoprenoids from Cestrum parqui
Brigida D¡¯Abrosca, Marina DellaGreca, Antonio Fiorentino, Pietro Monaco,Palma Oriano, Fabio Temussi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     blumenol C
    ÏàËÆ¶È:86.6%
Acta Botanica Yunnanica          2003          25(4)          503-506
An Ionone Derivative from Isodon leucophyllus
ZHAO Ai-Hua,PENGLi-Yan,WANG Zong-Yu,SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 6a
    ÏàËÆ¶È:86.6%
Chemical & Pharmaceutical Bulletin          1988          36          2475-2484
Studies on the Glycosides of Epimedium grandiflorum MORR. var. thunbergianum (MIQ.) NAKAI. III
TOSHIO MIYASE,AKIRA UENO,NOBUO TAKIZAWA,HIROMI KOBAYASHI and HIROKO OGUCHI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     9-hydroxymegastigm-4-en-3-one
    ÏàËÆ¶È:86.6%
Australian Journal of Chemistry          1989          42          2071-2084
Norisoprenoids in Vitis vinifera White Wine Grapes and the Identification of a Precursor of Damascenone in These Fruits
MA Sefton, GK Skouroumounis, RA Massywestropp and PJ Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     compound 1'
    ÏàËÆ¶È:86.6%
Chinese Traditional and Herbal Drugs          2012          43          1688-1690
Chemical constituents from Opuntia dillenii
WANG Zheng; QIU Ying-kun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     4-(3'(R)-hydroxybutyl)-3,5,5,trimethyl-cyclohex-2-en-1-one
C13H22O2     ÏàËÆ¶È:80%
Natural Product Research          2003          17          355-360
Isolation and Structure Determination of a Benzofuran and a Bis-Nor-Isoprenoid from Aspergillus Niger Grown on the Water Soluble Fraction of Morinda Citrifolia Linn. Leaves
Bina S. Siddiqui; Fouzia A. Sattar Ismail; Tahsin Gulzar; Sabira Begum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     ZP-amide B
C16H25NO4     ÏàËÆ¶È:66.6%
Phytochemistry          2004          65          2599-2604
Aliphatic acid amides of the fruits of Zanthoxylum piperitum
Tsutomu Hatano, Kazutoshi Inada, Tomo-omi Ogawa, Hideyuki Ito, Takashi Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     chinensiol
C30H50O3     ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1994          42          2187-2189
CHINENSIOL, A NEW DIMERIC HIMACHALANE-TYPE SESQUITERPENE FROM THE ROOT OF JUNIPERUS CHINENSIS LINN.
Yueh-Hsiung KUO and Wen-Ching CHEN
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     chinensiol
    ÏàËÆ¶È:66.6%
Chemical & Pharmaceutical Bulletin          1999          47          557-560
Five New cis-Himachalane-Type Sesquiterpenes from the Heartwood of Juniperus chinensis var. tsukusiensis
Lung-Lin SHIU,Wen-Ching CHEN and Yueh-Hsiung KUO
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     6R*-9,10-dihydroxy-4-megastigmen-3-one
C13H22O3     ÏàËÆ¶È:66.6%
Chinese Traditional and Herbal Drugs          2012          43          1688-1690
Chemical constituents from Opuntia dillenii
WANG Zheng; QIU Ying-kun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     compound 18
    ÏàËÆ¶È:62.5%
Journal of the Brazilian Chemical Society          2001          12          391-402
Synthesis of Rearranged Unsaturated Drimane Derivatives.
Domingos S. de Miranda, Gelson J. A. da Conceição, Julio Zukerman-Schpector, M¨¢rio C. Guerrero, Ulf Schuchardt, Angelo C. Pinto, Claudia M. Rezende and Anita J. Marsaioli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     9(S)-4-oxo-7,8-dihydro-¦Â-ionol
    ÏàËÆ¶È:60%
Phytochemistry          2008          69          2708-2715
Bioactive apocarotenoids from Tectona grandis
Francisco A. Mac¨ªas, Rodney Lacret, Rosa M. Varela, Clara Nogueiras, Jose M.G. Molinillo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     ZP-amide E
C16H27NO4     ÏàËÆ¶È:60%
Phytochemistry          2004          65          2599-2604
Aliphatic acid amides of the fruits of Zanthoxylum piperitum
Tsutomu Hatano, Kazutoshi Inada, Tomo-omi Ogawa, Hideyuki Ito, Takashi Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     ZP-amide F
C16H27NO4     ÏàËÆ¶È:60%
Phytochemistry          2004          65          2599-2604
Aliphatic acid amides of the fruits of Zanthoxylum piperitum
Tsutomu Hatano, Kazutoshi Inada, Tomo-omi Ogawa, Hideyuki Ito, Takashi Yoshida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3-epi-perforenone A
C15H22O2     ÏàËÆ¶È:60%
Journal of Natural Products          2003          66          435-437
Three New Sesquiterpenes from the Red Alga Laurencia perforata
Anthony D. Wright, Eva Goclik, and Gabriele M. Knig
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     13-carboxy2blumenol C
C13H20O4     ÏàËÆ¶È:60%
Acta Botanica Yunnanica          2003          25(4)          503-506
An Ionone Derivative from Isodon leucophyllus
ZHAO Ai-Hua,PENGLi-Yan,WANG Zong-Yu,SUN Han-Dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     14-[(2H3)Methyl]bicyclo[9.4.0]pentadec-1(11)-en-12-one
    ÏàËÆ¶È:60%
Helvetica Chimica Acta          2009          92          1782-1799
Synthesis of Deuterium-Labeled Perfume Ingredients as Internal Standards for Their GC/MS Quantification
Christian Chapuis, Carole Cantatore, Peter Fankhauser, Ren¨¦ Challand, Jean-Jacques Riedhauser
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     (E)-2-Methyl-5-(2exo-methyl-3-methylidene-bicyclo[2.2.1 ]hept-2-yl)-2-penten-l-ol( epi-(E)-¦Â-santalol
    ÏàËÆ¶È:60%
Helvetica Chimica Acta          1981          64          25-32
Stereoselective Syntheses of (¡À)-epi-¦Â-Santalene and (¡À)-epi-¦Â-Santalol
Roger L. Snowden, Philippe Sonnay, G¨¹unther Ohloff
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     hurghamide-D
C23H41NO3     ÏàËÆ¶È:60%
Natural Product Research          1997          9          281-288
Hurghamides A-D, New N-Acyl-2-Methylene-¦Â-Alanine Methyl Esters from Red sea Hippospongia SP
Yuewei Guo; Margherita Gavagnin; Ernesto Mollo; Guido Cimino; Nehal Aly Hamdy; Issa Fakhr; Maurizio Pansini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     14-hydroxy-¦Á-muurolene
    ÏàËÆ¶È:60%
Journal of Natural Products          1994          Vol 57          155
A Novel Diterpene Glycoside from the Soft Coral of Lemnalia bournei
Min Zhang, Kanghou Long, Houming Wu, Kan Ma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     14-hydroxy-¦Á-muurolene
C15H24O     ÏàËÆ¶È:60%
Phytochemistry          1991          30          1551-1554
Oxygenated sesquiterpenes from the wood of Juniperus oxycedrus
A.F. Barrero, J.F. S¨¢nchez, J.E. Oltra, J. Altarejos, N. Ferrol, A. Barrag¨¢n
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-12-10 09:09:32
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