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13C NMR (101 MHz, CDCl3) ¦Ä13.33,23.56,27.30,29.69,34.28,35.46,37.27,68.65,125.24,140.34, 199.30.
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fangfuhu123: ½ð±Ò+10, ¡ïÓаïÖú 2015-06-06 00:09:21
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1 .     compound 76
    ÏàËÆ¶È:83.3%
Journal of Agricultural and Food Chemistry          1990          38          1041-1048
Two-dimensional GC-DCCC analysis of the glycoconjugates of monoterpenes, norisoprenoids, and shikimate-derived metabolites from Riesling wine
Peter Winterhalter, Mark A. Sefton, Patrick J. Williams
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     9-Hydroxy-5,7-megastigmadien-4-one
    ÏàËÆ¶È:83.3%
Journal of Tropical and Subtropical Botany          2010          18          564-568
Chemical Constituents from Isodon lophanthoides var. gracilif lora
LIANG, Yao, guang, XU, Xinya, XIE, Hai, hui, LIN, Qing, WEI, Xiao, yi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     (4R)-1-bromo-4-methyldecane
C11H23Br     ÏàËÆ¶È:63.6%
European Journal of Organic Chemistry          2011                   5894-5904
Synthesis of Optically Pure Diglycerol Tetraether Model Lipids with Non-Natural Branching Pattern
Thomas Markowski, Simon Drescher, Annette Meister, Gerd Hause, Alfred Blume and Bodo Dobner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     2-methyloctanol
    ÏàËÆ¶È:63.6%
Natural Product Communications          2013          8          869-871
Structural Factors in the Odor of ¦Á-Santalol Derivatives
Toshio Hasegawa, Hiroaki Izumi and Hideo Yamada
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (7E,9¦Î)-9-hydroxy-5,7-megastigmadien-4-one
C13H20O2     ÏàËÆ¶È:61.5%
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
6 .     cytotoxic sesquiterpene caryol-7-en-6-ol
    ÏàËÆ¶È:60%
Helvetica Chimica Acta          2009          92          375-378
A New Tricyclo[6.3.1.02,5]dodecane Sesquiterpene from Cultures of the Basidiomycete Campanella junghuhnii
Rong Liu, Zhong-Yu Zhou, Di Xu, Fei Wang, Ji-Kai Liu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     sesquiterpene
C15H24O     ÏàËÆ¶È:60%
Australian Journal of Chemistry          1988          41          1755-1761
Sesquiterpenes From a New Zealand Sponge of the Genus Eurypon
CJ Barrow, JW Blunt and MHG Munro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     isofurocaespitane
C12H16OBrCl     ÏàËÆ¶È:58.3%
Tetrahedron letters          1979          20          2719-2722
Carbon-13 NMR application to Laurencia polyhalogenated sesquiterpenes
A.G. Gonz¨¢lez, J.D. Mart¨ªn, V.S. Mart¨ªn, M. Norte
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (R)-3-Methyloctyl-4-methylbenzenesulfonate
    ÏàËÆ¶È:57.1%
Chemistry of Natural Compounds          2010          46          440-443
Stereoselective synthesis of the sex pheromone of the yellow mealworm using (S)-4-benzyloxazolidinone as chiral auxiliary
D. L. Li, C. F. Lu, G. C. Yang and Z. X. Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     (2E,4R,5S)-2-ethylidene-5-(methoxycarbonyl)-4-methylhexano-5-lactone
C11H16O4     ÏàËÆ¶È:54.5%
Helvetica Chimica Acta          2007          Vol. 90          1028
Sesquiterpenoids and Lactone Derivatives from Ligularia dentata
Hitomi Baba, Yasunori Yaoita, and Masao Kikuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     ((5-butyltetrahydrofuran-2-yl)ethynyl)trimethylsilane(Major isomer)
C19H24OSi     ÏàËÆ¶È:54.5%
Organic Letters          2007          Vol. 9, No. 10          1975-1978
Ene-yne Tetrahydrofurans from the Sponge Xestospongia muta. Exploiting a Weak CD Effect for Assignment of Configuration
Brandon I. Morinaka, Colin K. Skepper, and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     ((5-butyltetrahydrofuran-2-yl)ethynyl)trimethylsilane(Minor isomer)
C19H24OSi     ÏàËÆ¶È:54.5%
Organic Letters          2007          Vol. 9, No. 10          1975-1978
Ene-yne Tetrahydrofurans from the Sponge Xestospongia muta. Exploiting a Weak CD Effect for Assignment of Configuration
Brandon I. Morinaka, Colin K. Skepper, and Tadeusz F. Molinski
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     N-Ethylpiperidin-4-ylmethyl valerate
C13H25NO2     ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry Letters          2004          14          1927-1930
N-[18F]fluoroethylpiperidin-4-ylmethyl butyrate: a novel radiotracer for quantifying brain butyrylcholinesterase activity by positron emission tomography
Tatsuya Kikuchi, Ming-Rong Zhang, Nobuo Ikota, Kiyoshi Fukushi, Toshimitsu Okamura, Kazutoshi Suzuki, Yasushi Arano, Toshiaki Irie
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     (4aS,8S )-4a-methyl-8- hydroxy-4 ,4a,5,6,7,8-hexahydro-2(3 H )naphthalenone
    ÏàËÆ¶È:54.5%
Bioorganic & Medicinal Chemistry Letters          1997          7          587-592
Regio- and stereoselective aspects in the oxidation of (R) and (S) 4a-methyl-(4,4a,5,6,7,8)-hexahydro-2(3H)naphthalenones in living rats
Philippe V¨¦rit¨¦, Sabine M¨¦nager, Christian Cav¨¦, Dominique Andr¨¦, Jean d'Angelo, Gilbert Revial, Claude Combet Farnoux, Olivier Lafont
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     (2S,6R)-2,6-Dimethyl-1,8-octanediol
    ÏàËÆ¶È:54.5%
Chemistry of Natural Compounds          2010          46          305-307
Chemical constituents from Incarvillea delavayi
Yun-Heng Shen, Tao Lu, Jian Tang, Run-Hui Liu and Hui-Liang Li, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     (R)-4-Methylnonanenitrile
    ÏàËÆ¶È:54.5%
Chemistry of Natural Compounds          2010          46          440-443
Stereoselective synthesis of the sex pheromone of the yellow mealworm using (S)-4-benzyloxazolidinone as chiral auxiliary
D. L. Li, C. F. Lu, G. C. Yang and Z. X. Chen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     4,4a,5,6,7,8-Hexahydronaphthalen-2(3H)-one
C10H14O     ÏàËÆ¶È:54.5%
Zeitschrift f¨¹r Naturforschung B          2005          60          984-989
Synthesis of Decaline Analogues of Isovelleral
M. Johansson, I. Aujard, D. Röme, H. Anke, and O. Sterner
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     ethyl(Z)-6-methyl-4-octenoate
C11H20O2     ÏàËÆ¶È:54.5%
Tetrahedron          1993          49          6569-6574
Isolation and synthesis of caprolactins A and B, new caprolactams from a marine bacterium
Bradley S. Davidson, Robert W. Schumacher
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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