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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½51¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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