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1 . (¨C)-Pinoresinol-4-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:96.2% Chemistry of Natural Compounds 2008 44 648-650 LIGNANS FROM Daphne giraldii Juan Su, Zhijun Wu, Yunheng Shen,Chuan Zhang, and Weidong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (+)-pinoresinol-¦Â-D-glucoside ÏàËÆ¶È:96.2% Journal of Chinese Pharmaceutical Sciences 1998 7 49-51 A Novel Lignan Glucoside from Forsythia suspensa Vahl Dong - Lei Liu , Sui - Xu Xu and Wei - Fang Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ËÉÖ¬ËØ-4-O-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:96.2% Chinese Traditional and Herbal Drugs 2010 41 201-203 °×¸½×ӵĻ¯Ñ§³É·ÖÑо¿ °¬·ïΰ; ÕÅáÔ; ÀîÑÞ·ï; ÂíÓ¢Àö Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (+)pinoresinol 4'-O-¦Â-D-glucopyranoside ÏàËÆ¶È:96.2% Chinese Journal of Natural Medicines 2003 1 199-203 Studies on Lignan Constituents of Clematis armandii Franch HUANG Wen-Wu; KONG De-Yun; YANG Pei-Ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (− -pinoresinol-4-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:96.2% Chinese Journal of Natural Medicines 2008 6 411-414 Chemical Constituents from Daphne koreana Nakai HU Xiao-Jia,JIN Hui-Zi,SU Juan,ZHANG Wei,XU Wen-Zheng,YAN Shi-Kai,LIU Run-Hui,LÜ Hui-Zi,ZHANG Wei-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . pinoresinol-¦Â-D-glucoide ÏàËÆ¶È:96.2% Journal of Shenyang Pharmaceutical University 1997 14 157-197 Lignan Glucosides of Forsythia Suspensa Vahl. Liu Donglei, Xu Suixu, Li Huiqing, Cui Wei, Fang Bing, Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (+)-pinoresinol-¦Â-D-glucoside ÏàËÆ¶È:96.2% Natural Product Research and Development 2004 16 391-394 CHEMICAL CONSTITUENTS FROM SAUSSUREA STELLA SHEN Jin; LIANG Jian; PENG Shu-lin; DING Li-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (+)-pinoresinol-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:92.5% Chinese Journal of Natural Medicines 2003 1 79-81 Studies on the Chemical Constituents of Fraxinus chinensis Roxb. ZHANG Dong Mei; HU Li Hong; YE Wen Cai; ZHAO Shou Xun Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-04-06 07:01:18
nkx1979
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µÚ¶þ¸ö 1 . (E)-diol ÏàËÆ¶È:60% Phytochemistry 2006 67 584-588 A hemiterpene glucoside as a probing deterrent of the bean aphid,Megoura crassicauda, from a non-host vetch, Vicia hirsuta Naohiro Ohta, Naoki Mori, Yasumasa Kuwahara, Ritsuo Nishida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (Z)-diol ÏàËÆ¶È:60% Phytochemistry 2006 67 584-588 A hemiterpene glucoside as a probing deterrent of the bean aphid,Megoura crassicauda, from a non-host vetch, Vicia hirsuta Naohiro Ohta, Naoki Mori, Yasumasa Kuwahara, Ritsuo Nishida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (E)-2-methyl-2-butene-1,4-diol ÏàËÆ¶È:60% Phytochemistry 2006 67 584-588 A hemiterpene glucoside as a probing deterrent of the bean aphid,Megoura crassicauda, from a non-host vetch, Vicia hirsuta Naohiro Ohta, Naoki Mori, Yasumasa Kuwahara, Ritsuo Nishida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (Z)-2-methyl-2-butene-1,4-diol ÏàËÆ¶È:60% Phytochemistry 2006 67 584-588 A hemiterpene glucoside as a probing deterrent of the bean aphid,Megoura crassicauda, from a non-host vetch, Vicia hirsuta Naohiro Ohta, Naoki Mori, Yasumasa Kuwahara, Ritsuo Nishida Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . compound 12 ÏàËÆ¶È:60% Helvetica Chimica Acta 1981 64 2571-2586 Umlagerung von ¦Á-Halogen- in ¦Á¡ä-Halogen-cyclobutanone, Schl¨¹sselstufe einer variationsreichen Synthese von Pyrethroiden Pierre Martin, Hans Greuter, Tammo Winkler, Daniel Belluš, Grety Rihs Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 1-acetylazetidine-3-thiol C5H9N ÏàËÆ¶È:60% Heterocycles 2009 78 1777-1786 Reaction of 1-Azabicyclo[1.1.0]butane with Activated Amides Kazuhiko Hayashi, Eiko Kujime, Hajime Katayama, Shigeki Sano, and Yoshimitsu Nagao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 3,9,10-trioxa-6-aza-1-silabicyclo[4.3.3]dodecan-1-amine ÏàËÆ¶È:60% Russian Journal of Organic Chemistry 2008 44 1543-1546 Reaction of sodium amide with 1-chloromethylsilatrane N. F. Lazareva and I. M. Lazarev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 5 ÏàËÆ¶È:60% Organic Magnetic Resonance 1983 21 426-428 13C nuclear magnetic resonance and conformational analysis of 5-chloro-2-oxo-1,3,2-dioxathianes Jean-Pierre Gorrichon, G¨¦rard Chassaing and Louis Cazaux Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . pent-3-en-2-ol ÏàËÆ¶È:60% Organic Magnetic Resonance 1984 22 428-430 Glucosidation shifts of allylic and benzylic alcohols in 13C NMR spectroscopy Isao Horibe, Shujiro Seo, Yohko Yoshimura and Kazuo Tori Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . CHCl2CH2CCl2CH2CHCl2 ÏàËÆ¶È:60% Organic Magnetic Resonance 1984 22 792-793 1H and 13C NMR study of vinyl chloride telomers with carbon tetrachloride J. M. Bessi¨¨re, B. Boutevin, M. Taha and F. Vial Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 2-Methyl-3-phenyloxirane ÏàËÆ¶È:57.1% Tetrahedron 2012 68 8493-8501 Asymmetric vanadium- and iron-catalyzed oxidations: new mild (R)-modafinil synthesis and formation of epoxides using aqueous H2O2 as a terminal oxidant Kerstin A. Stingl, Katharina M. Weiß, Svetlana B. Tsogoeva Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2013-04-06 07:02:03
nkx1979
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µÚÈý¸ö 1 . (RS)-2-amino-N-(2,6-dimethylphenyl)-3-hydroxypropanamide©qHCl C11H16N2O2 ÏàËÆ¶È:62.5% Journal of Heterocyclic Chemistry 2011 48 261-266 Facile routes for the preparation of 3,4-disubstituted 1,3-oxazolidines and 1,2,5-trisubstituted imidazolidin-4-ones Alessia Catalano, Alessia Carocci, Giovanni Lentini, Antonia Di Mola, Claudio Bruno and Carlo Franchini Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 2-hydroxy-4-isocyano-¦Á-methyl-6-oxabicyclo[3.1.0]hex-3-ene-2-methanol C8H9NO3 ÏàËÆ¶È:62.5% The Journal of Antibiotics 1997 50 474-478 MR566A and MR566B, New Melanin Synthesis Inhibitors Produced by Trichoderma harzianum II. Physico-chemical Properties and Structural Elucidation CHOONG HWAN LEE, HIROYUKI KOSHINO, MYUNG CHUL CHUNG, HO JAE LEE, JONG KI HONG, JONG SHIN YOON, YUNG HEE KHO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 3-ethyl-5-methylpyridine ÏàËÆ¶È:62.5% Organic Magnetic Resonance 1984 22 621-623 Proximity effect in the 13C NMR spectra of alkylpyridines: An aid in structure elucidation Miroslav Hol¨ªk, Milena Turečkov¨¢ and Jan Vym¨§tal Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 10 C14H14N2O4S ÏàËÆ¶È:55.5% Tetrahedron Letters 2002 43 2145-2147 Direct synthesis of thioethers from sulfonyl chlorides and activated alcohols Michael T Martin, Alford M Thomas, Douglas G York Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 5-(methoxymethyl)-1H-pyrrole-2-carbaldehyde C7H9NO2 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 1066-1070 Nitrogen-Containing Compounds from Salvia miltiorrhiza Ming-Jaw Don, Chien-Chang Shen, Yun-Lian Lin, Wan-Jr Syu, Yi-Huei Ding, and Chang-Ming Sun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 3 C7H10O5 ÏàËÆ¶È:50% Chemistry of Natural Compounds 2005 41 243-244 METABOLITES OF THE MARINE FUNGUS Asperigillus varians KMM 4630 O. F. Smetanina, A. I. Kalinovskii, Yu. V. Khudyakov,O. P. Moiseenko, M. V. Pivkin, N. I. Menzorova,Yu. T. Sibirtsev, and T. A. Kuznetsova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 4-(Triethoxysilyl)acetophenone ÏàËÆ¶È:50% Molecules 2008 13 2601-2607 The Synthesis of 1-(4-Triethoxysilyl)phenyl)-4, 4, 4-trifluoro-1, 3-butanedione, a Novel Trialkoxysilane Monomer for the Preparation of Functionalized Sol-gel Matrix Materials Christopher J. Peeples, Raghu R. Earni and John C. DiCesare Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (-)-cathinone ÏàËÆ¶È:50% Journal of Natural Products 1987 Vol 50 1138 (-)-Cathinone: Improved Synthesis and Carbon-13 NMR Assignments Ibrahim A. al-Meshal, Khalid A. al-Rashood, Mohammad Nasir, Farouk S. el-Feraly Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 4-(3,4-dihydroxy-(E)-1-pentenyl)-oxazole C8H11NO3 ÏàËÆ¶È:50% Journal of Natural Products 1995 Vol 58 1605-1607 MR-93A, a New Oxazole from Trichoderma harzianum KCTC 0114BP Choonghwan Lee, Myungchul Chung, Hojae Lee, Yunghee Kho, Hiroyuki Koshino Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2013-04-06 07:02:52
nkx1979
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bravexueli: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ¸ÐлÄúµÄ°ïÖú 2013-04-06 09:38:14
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µÚÒ»¸ö 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 53.6,53.7,55.5,55.6,60.7,69.7,70.9,71.0,73.2,76.9,77.1,84.9,85.2,100.2,110.4,110.6,115.2,115.3,118.3,118.7,132.2,135.3,145.8,145.9,147.6,149.0,174.1 ÈܼÁÑ¡Ï È«²¿ CDCl3 CD3CD2OD CD2Cl2 C5D5N C3D7NO CD3SOCD3 C4D8O (CH3)4Si C4D8O2 CD3COOD C4D8O2 H2O D2O CF3COOD CD3OD ND3 CD3COCD3 C6D6 CD3CN ²éѯ¿ÕÖµ Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½337¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . (¨C)-Pinoresinol-4-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:96.2% Chemistry of Natural Compounds 2008 44 648-650 LIGNANS FROM Daphne giraldii Juan Su, Zhijun Wu, Yunheng Shen,Chuan Zhang, and Weidong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (+)-pinoresinol-¦Â-D-glucoside ÏàËÆ¶È:96.2% Journal of Chinese Pharmaceutical Sciences 1998 7 49-51 A Novel Lignan Glucoside from Forsythia suspensa Vahl Dong - Lei Liu , Sui - Xu Xu and Wei - Fang Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . ËÉÖ¬ËØ-4-O-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:96.2% Chinese Traditional and Herbal Drugs 2010 41 201-203 °×¸½×ӵĻ¯Ñ§³É·ÖÑо¿ °¬·ïΰ; ÕÅáÔ; ÀîÑÞ·ï; ÂíÓ¢Àö Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (+)pinoresinol 4'-O-¦Â-D-glucopyranoside ÏàËÆ¶È:96.2% Chinese Journal of Natural Medicines 2003 1 199-203 Studies on Lignan Constituents of Clematis armandii Franch HUANG Wen-Wu; KONG De-Yun; YANG Pei-Ming Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (− -pinoresinol-4-O-¦Â-D-glucopyranoside C26H32O11 ÏàËÆ¶È:96.2% Chinese Journal of Natural Medicines 2008 6 411-414 Chemical Constituents from Daphne koreana Nakai HU Xiao-Jia,JIN Hui-Zi,SU Juan,ZHANG Wei,XU Wen-Zheng,YAN Shi-Kai,LIU Run-Hui,LÜ Hui-Zi,ZHANG Wei-Dong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . pinoresinol-¦Â-D-glucoide ÏàËÆ¶È:96.2% Journal of Shenyang Pharmaceutical University 1997 14 157-197 Lignan Glucosides of Forsythia Suspensa Vahl. Liu Donglei, Xu Suixu, Li Huiqing, Cui Wei, Fang Bing, Structure 13C NMR ̼Æ×Ä£Äâͼ |

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