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1 .     Anisocumarin H
C19H22O4     ÏàËÆ¶È:63.1%
Journal of Natural Products          1989          Vol 52          243
Prenylated Coumarins from the Leaves of Clausena anisata
Bonaventure Tchaleu Ngadjui, Johnson Foyere Ayafor, Beibam Lucas Sondengam, Joseph Donald Connolly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     eremophila-10,11-diene-7¦Á, 13-diol
C15H24O2     ÏàËÆ¶È:53.3%
Planta Medica          1997          63          248-250
A New Eremophilane Sesquiterpenoid and a New Iridoid from Pedicularis striata subsp. arachnoides
Jianjun Gao, Li Yang, and Zhongjian jia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     compound 5h
C29H31N2Cl3O4     ÏàËÆ¶È:53.3%
Molecules          1997          2          91-98
Synthesis and Characterization of Heptamethine Cyanine Dyes
Qun Li, Ji Tan and Bi Xian Peng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     eremophila-10,11-dien-7¦Á,13-diol
C15H24O2     ÏàËÆ¶È:53.3%
Phytochemistry          1996          43          1411-1412
An eremophilane sesquiterpenoid from Pedicularis striata pall SSP. Arachnoidea
Jian-Jun Gao, Zhong-Jian Jia, Carles Codina
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     1-(2-Methyl-1,2,3,4-tetrahydroquinolin-4-yl)pyrrolidin-2-one
C14H18N2O     ÏàËÆ¶È:53.3%
Canadian Journal of Chemistry          2010          88          443-452
Imino Diels-Alder reaction - An efficient synthetic protocol for 2-methyl-4-substituted tetrahydroquinolines catalyzed by copper dipyridine dichloride
C.S. Kavitha, K.M. Hosamani, and R.S. Harisha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     1-(6-Fluoro-2-methyl-1,2,3,4-tetrahydroquinolin-4-yl)pyrrolidin-2-one
C14H17FN2O     ÏàËÆ¶È:53.3%
Canadian Journal of Chemistry          2010          88          443-452
Imino Diels-Alder reaction - An efficient synthetic protocol for 2-methyl-4-substituted tetrahydroquinolines catalyzed by copper dipyridine dichloride
C.S. Kavitha, K.M. Hosamani, and R.S. Harisha
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     (¡À)-(2R,3R)-3-hydroxymethyl-2,3-dimethyl-1,2,3,4-tetra-hydroquinoline
C12H17NO     ÏàËÆ¶È:53.3%
Journal of Heterocyclic Chemistry          2007          44          1051-1057
(¡À)-2,3-dialkyl-1,2,3,4-tetrahydroquinoline-3-carboxylic esters by a tandem reduction-reductive amination reaction
Richard A. Bunce,James E. Schammerhorn and LeGrande M. Slaughter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     (7S,10R)-(+)-10,11-epoxycurcuphenol
C15H22O2     ÏàËÆ¶È:53.3%
Heterocycles          2009          78          2595-2600
Curcuphenol Derivatives from the Gorgonian Echinomuricea Sp.
Hsu-Ming Chung, Tsong-Long Hwang, Wei-Hsien Wang, Lee-Shing Fang, and Ping-Jyun Sung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (1R,1'R)-2-(1-p-Toluenesulfoxyethyl)-6-[1'-(N-piperidinyl)ethyl]pyridine
C21H28N2O3S     ÏàËÆ¶È:53.3%
Heterocycles          2007          72          449-458
Stereo Differenciated Synthesis of Optically Pure 2-[1-(1-Phenylethylamino)ethyl]-6-[1-(N-piperidinyl)ethyl]pyridines
Jun'ichi Uenishi, Taro Takami, and Sachiko Aburatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     1,2-dimethyl-4-tosyl-1,4-cyclohexadiene
C15H18O2S     ÏàËÆ¶È:53.3%
Heterocycles          2006          70          619-626
Synthesis of 4,7-Dihydro-2H-isoindole Derivatives via Diels-Alder Reaction of Tosylacetylene
Tetsuo Okujima,* Guangnan Jin, Yusuke Hashimoto, Hiroko Yamada, Hidemitsu Uno, and Noboru Ono*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     (E)-3,7,11-Trimethyl-1,6,10-dodecatrIene-3,5-diol
C15H26O2     ÏàËÆ¶È:53.3%
Phytochemistry          1985          24          1729-1733
Oxygenated nerolidol derivatives from Artemisia alba
Giovanni Appendino, Pierluigi Gariboldi, Francesco Menichini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     (E,E)-11-Hydroperoxy-3,7,1l-trimethyl-1,6,9-dodecotrien-3,5-diol
    ÏàËÆ¶È:53.3%
Phytochemistry          1985          24          1729-1733
Oxygenated nerolidol derivatives from Artemisia alba
Giovanni Appendino, Pierluigi Gariboldi, Francesco Menichini
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (6E)5,9-dihydroxynerolidol
    ÏàËÆ¶È:53.3%
Phytochemistry          1986          25          185-190
Tetracyclic triterpenes and nerolidol derivatives from Santolina oblongifolia
J. De Pascual Teresa, I.S. Bellido, M.S. Gonz¨¢lez, S. Vicente
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     nerolidol
    ÏàËÆ¶È:53.3%
Phytochemistry          1986          25          739-740
9-acetoxynerolidol from Phrodus bridgesii
Vicente Gambaro, Marisa Piovano, Juan A. Garbarino
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
Domyallbesttohaveahappylife.
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