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jiangtao2956
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GT
- Ó¦Öú: 123 (¸ßÖÐÉú)
- ½ð±Ò: 4525.1
- É¢½ð: 43
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- Ìû×Ó: 648
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- ³æºÅ: 1139122
- ×¢²á: 2010-11-04
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2Â¥2014-12-19 20:38:49
xuqian092
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- ½ð±Ò: 401.5
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3Â¥2014-12-22 10:30:04
xuqian092
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- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 401.5
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- רҵ: ÌìÈ»Óлú»¯Ñ§
4Â¥2014-12-22 17:43:37
jiangtao2956
ľ³æ (ÕýʽдÊÖ)
GT
- Ó¦Öú: 123 (¸ßÖÐÉú)
- ½ð±Ò: 4525.1
- É¢½ð: 43
- ºì»¨: 4
- Ìû×Ó: 648
- ÔÚÏß: 110Сʱ
- ³æºÅ: 1139122
- ×¢²á: 2010-11-04
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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 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½5¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1,5-dimethyl citrate ÏàËÆ¶È:60% Journal of Shenyang Pharmaceutical University 2009 26 807-810 Isolation and identification of chemical constituents from the fruit and calyx of Physalis alkekengi L. var. franchetii(Mast.)Makino CAI Qian, LIU Yu-qiang, MA Zhe Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1,5-dimethyl citrate ÏàËÆ¶È:60% Natural Product Research and Development 2009 21 731-732 Studies on the Metabolites of Aspergillus aculeatus YM 311498,an Endophytic Fungus from Azadirachta indica A.Juss WU Shao-hua; CHEN You-wei; SHAO Shi-cheng; LI Zhi-ying; YANG Li-yuan; LI Shao-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . dimethyl 3-carboxyl-3-hydroxy pentanedioate ÏàËÆ¶È:60% Journal of Chinese Medicinal Materials 2003 26 867-869 Studies on Constituents of Rosa bracteata Fruits(¢ò) Xu Zhiguo, Huang Song, Du Fanglu, Peng Caiyun, Tian Yuwang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-hydroxy-3-methoxycarbonyl pentanedioic acid ÏàËÆ¶È:60% Journal of Chinese Medicinal Materials 2003 26 867-869 Studies on Constituents of Rosa bracteata Fruits(¢ò) Xu Zhiguo, Huang Song, Du Fanglu, Peng Caiyun, Tian Yuwang Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . citric acid C6H8O7 ÏàËÆ¶È:50% Journal of China Pharmaceutical University 2005 36 520-522 Chemical Constituents of Evodia rutaecarpa WANG Qi-Zhi; LIANG Jing-Yu; CHEN Jun Structure 13C NMR ̼Æ×Ä£Äâͼ |

5Â¥2014-12-22 20:07:40
jiangtao2956
ľ³æ (ÕýʽдÊÖ)
GT
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- ½ð±Ò: 4525.1
- É¢½ð: 43
- ºì»¨: 4
- Ìû×Ó: 648
- ÔÚÏß: 110Сʱ
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µÚ¶þ¸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 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½5¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . cytochalasin P C30H41NO6 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1987 35 902-905 THREE NEW 10-PHENYL- [11] CYTOCHALASANS, CYTOCHALASINS N, O, AND P FROM PHOMOPSIS SP Takako Tomioka,Yoshihiko Izawa,Kiyotaka Koyama and Shinsaku Natori Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . N-(2-p-Tolyltetrahydropyran-4-yl)acetamide C14H19NO2 ÏàËÆ¶È:50% Canadian Journal of Chemistry 2009 87 698-705 Cerium(IV) sulfate catalyzed one-pot threecomponent diastereo selective synthesis of 4-amidotetrahydropyrans Nagarajan Panneer Selvam and Paramasivan T. Perumal Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3aR,5,5,7aS-tetramethylhexahydroimidazo[4,5-b]pyrazine-2-thione C9H18N4S ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2009 57 1371-1375 Tetraazaindenes Derived from Dihydropyrazines with DNA Strand-Breaking Activity Kazuhide Nakahara, Shinji Takechi, Koki Yamaguchi, Kazunobu Harano and Tadatoshi Yamaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . N-(2-p-tolyltetrahydropyran-4-yl)-acetamide C14H19NO2 ÏàËÆ¶È:50% Indian Journal of Chemistry Section B 2011 50B 1083-1091 Iodine/AcCl-catalyzed Prins-Ritter reaction: Synthesis of 4-amido tetrahydropyrans Srinivasan, P; Perumal, P T; Raja, S Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 12n C13H25N3O3 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2012 20 3807-3815 Design, synthesis and biological evaluation of novel amino acid ureido derivatives as aminopeptidase N/CD13 inhibitors Li Su, Yuping Jia, Lei Zhang, Yingying Xu, Hao Fang, Wenfang Xu Structure 13C NMR ̼Æ×Ä£Äâͼ |

6Â¥2014-12-22 20:08:39
jiangtao2956
ľ³æ (ÕýʽдÊÖ)
GT
- Ó¦Öú: 123 (¸ßÖÐÉú)
- ½ð±Ò: 4525.1
- É¢½ð: 43
- ºì»¨: 4
- Ìû×Ó: 648
- ÔÚÏß: 110Сʱ
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µÚ¶þ¸ö È«²¿ÈܼÁ 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£º¹²²éµ½132¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 1,2,3,6-tetra-O-acetyl-5-deoxy-¦Á,¦Â-L-arabino-hexofuranose(¦Â-anomer) C14H20O9 ÏàËÆ¶È:61.5% Bioorganic & Medicinal Chemistry 2010 18 5339-5345 Synthesis of 5-deoxy-¦Â-d-galactofuranosides as tools for the characterization of ¦Â-d-galactofuranosidases Andrea Bordoni, Rosa M. de Lederkremer, Carla Marino Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1¦Â,6¦Á,8¦Â-trihydroxy-11,13-dihydroeudesm-4-en-6-olide 8-acetate C17H24O5 ÏàËÆ¶È:58.8% Phytochemistry 1990 29 1689-1690 Eudesmanolides from Stevia aff. tomentosum Mariano Mart¨ªnez-Vazquez,Rosa Elena Gallegos,Pedro Joseph-Nathan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-C-(R-Propan-2'-ol)-3,5-di-O-acetyl-2,2'-anhydro-¦Á-D-ribofuranoside ÏàËÆ¶È:58.3% Canadian Journal of Chemistry 2006 84 597-602 Stereoselective synthesis of dioxabicycles from 1-C-allyl-2-O-benzyl-glycosides - An intramolecular cyclization between 2-O-benzyl oxygen and the allyl double bond1 An-Tai Wu, Tian Yi, Huawu Shao, Shih-Hsiung Wu, and Wei Zou Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (-)-p-menthanetriol ÏàËÆ¶È:58.3% Bioscience, Biotechnology, and Biochemistry 2003 67 475-479 (+)-Menthol and Its Hydroxy Derivatives, Novel Fungal Monoterpenols from the Fusicoccin-producing Fungi, Phomopsis amygdali F6a and Niigata 2 Takeshi SASSA, Hiromichi KENMOKU, Mitsuyoshi SATO, Tetsuya MURAYAMA and Nobuo KATO Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 52 C19H37O4ISi ÏàËÆ¶È:58.3% Tetrahedron 2013 69 7746-7758 Stereoselectivity of electrophile-promoted oxacyclizations of 1,4-dihydroxy-5-alkenes to 3-hydroxytetrahydropyrans Frank E. McDonald, Kento Ishida, Jessica A. Hurtak Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 2 ÏàËÆ¶È:58.3% Magnetic Resonance in Chemistry 1990 28 659-660 1H and 13C NMR study of the neomenthyl halides: A very high field proton shift in the iodide Gordon L. Lange and Christine Gottardo Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . pericyclocamphanone ÏàËÆ¶È:58.3% Organic Magnetic Resonance 1973 5 277-283 Carbon-13 chemical shifts of substituted nortricyclenes E. Lippmaa, T. Pehk and J. Paasivirta Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (1¦Á,4a¦Â,8a¦Â)-4a-methyldecahydronaphthalene-1,8a-diol ÏàËÆ¶È:58.3% Australian Journal of Chemistry 1981 34 1451-1465 Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols JM Coxon and JR Gibson Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (4a¦Á,5¦Â,8a¦Á)-5-acetoxy-8a-methyldecahydronaphthalen-4a-ol ÏàËÆ¶È:58.3% Australian Journal of Chemistry 1981 34 1451-1465 Carbon-13 N.M.R. studies of 5¦Á- and 5¦Â-Cholestan-5-ols and analogous 8a-Methyl-trans- and cis-decahydronaphthalen-4a-ols JM Coxon and JR Gibson Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . [3-(N-Acetyl-N-methyl-amino)-propyl]-phosphonic acid ÏàËÆ¶È:58.3% Bioorganic & Medicinal Chemistry 2006 14 2375-2385 Evaluation of fosmidomycin analogs as inhibitors of the Synechocystis sp. PCC6803 1-deoxy-d-xylulose 5-phosphate reductoisomerase Youn-Hi Woo, Roberta P.M. Fernandes, Philip J. Proteau Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 1¦Â,4¦Â,5¦Á-trihydroxy-6¦Â-acetoxyeudesmane C17H30O5 ÏàËÆ¶È:56.2% Journal of Natural Products 1988 Vol 51 475 Epoxidation Reaction of 6¦Â-Acetoxyeudesmenes and Acid-catalyzed Transformations of the Epoxy Compounds E. Cabrera, A. Garcia-Granados, M. A. Quecuty Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . jioglutin C triacetae C16H22O9 ÏàËÆ¶È:56.2% Phytochemistry 1989 28 2385-2391 Five cyclopentanoid monoterpenes from Rehmannia glutinosa Takashi Morota,Hiroaki Nishimura,Hiroshi Sasaki,Masao Chin (Chen Zhengxiong),Kô Sugama,Takao Katsuhara,Hiroshi Mitsuhashi Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . (E and Z)-N-[(1R*,2R*)-2-Chloro-1,3-dimethylbutyl]-N'-[(4-methylphenyl)sulfonyl]ethanimidamide C15H23ClN2O2S ÏàËÆ¶È:53.8% Helvetica Chimica Acta 2010 93 233-241 Copper-Catalyzed Ritter-Type Reaction of Unactivated Alkenes with Dichloramine-T Takumi Abe, Hiroyuki Takeda, Yoshihisa Miwa, Koji Yamada, Reiko Yanada and Minoru Ishikura Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 2-(2,4,6-trimethyl-phenyl)-tetrahydro-pyrazolo[1,2-a]pyridazine-1,3-dione C16H20N2O2 ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2009 17 4241-4256 Aryldiones incorporating a [1,4,5]oxadiazepane ring. Part I: Discovery of the novel cereal herbicide pinoxaden Michel Muehlebach, Manfred Boeger, Fredrik Cederbaum, Derek Cornes, Adrian A. Friedmann, Jutta Glock, Thierry Niderman, Andr¨¦ Stoller, Trixie Wagner Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . hippodamine ÏàËÆ¶È:53.8% Magnetic Resonance in Chemistry 1999 37 60-64 Complete assignment of the 1H and 13C NMR spectra of the Coccinellidae-defensive alkaloids myrrhine, precoccinelline and hippodamine, their N -oxides and the corresponding hydrochlorides B. Lebrun, J. C. Braekman and D. Daloze Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (¡À)-(4aS,8aR)-2,5,5,8a-Tetramethyl-cis-4a,5,6,7,8,8ahexahydro-4H-1-benzopyran ÏàËÆ¶È:53.8% Flavour and Fragrance Journal 2006 21 659-666 Synthesis and odour evaluation of stereoisomers of octahydrobenzopyran derivatives Pablo J. Linares-Palomino, Sof¨ªa Salido, Joaqu¨ªn Altarejos, Manuel Nogueras and Adolfo S¨¢nchez Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 2-(c-3-Acetoxy-1,2,2-trimethyl-r-1-cyclopentyl)propanedinitrle C13H18N2O2 ÏàËÆ¶È:53.8% Helvetica Chimica Acta 1995 78 2065-2076 Cascade Cyclizations of Terpenoid Polyalkenes Triggered by Photoelectron Transfer ¨C Biomimetics with Photons Klaus-Dieter Warzecha, Xuechao Xing, Martin Demuth, Richard Goddard, Magnus Kessler and Carl Kr¨¹ger Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 22b ÏàËÆ¶È:53.8% Magnetic Resonance in Chemistry 1994 32 732-738 13C NMR of 4,5-epoxy-3-substituted decalin and analogous ¦¤4-octalin derivatives: Epoxide- and methyl-induced shifts Adrian Martin Pohlit and Helena Maria Carvalho Ferraz Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 4¦Â,7¦Â,11-enantioeudesmantriol C15H28O3 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2007 55(3) 376-381 Two Minor Diterpene Glycosides and an Eudesman Sesquiterpene from Coleus forskohlii Yupei SHAN,Xiaobing WANG,Xiang ZHOU,Lingyi KONG,and Masatake NIWA Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . chrysothol C15H26O2 ÏàËÆ¶È:53.3% Phytochemistry 2006 67 1547-1553 Constituents of Chrysothamnus viscidiflorus Ahmed A. Ahmed , Mohamed-Elamir F. Hegazy, Nahed M. Hassan,Malgorzata Wojcinska, Joe Karchesy, Paul W. Pare, Tom J. Mabry Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 4¦Â-hydroxy-4, 10¦Á-dimethyl-7¦ÁH,8¦ÁH-eudesman-11-ene-8,12-olide C15H22O3 ÏàËÆ¶È:53.3% Phytochemistry 2004 65 2039-2043 Constituents of two Flourensia species Mar¨ªa L. Uriburu, Juana R. de la Fuente, Jorge Palermo, Roberto R. Gil,Virginia E. Sosa Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . (-)-7¦ÂH-eudesmane-4¦Á,11-diol C15H28O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1998 61 22-28 Enantioselective Total Syntheses of (-)-7¦ÂH-Eudesmane-4¦Á, 11-diol and (+)-ent-7¦ÂH-Eudesmane-4¦Á, 11-diol Fumito Shimoma, Hisao Kondo, Saori Yuuya, Toshio Suzuki, Hisahiro Hagiwara, and Masayoshi Ando Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . Buchariol C15H26 O2 ÏàËÆ¶È:53.3% Molecules 2005 10 971-977 Terpenoids from Cleome droserifolia (Forssk.) Del Hesham I. El-Askary Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . Pterodondiol ÏàËÆ¶È:53.3% Journal of Asian Natural Products Research 2007 9 277-283 Sesquiterpenoids from Hedychium yunnanense and Porana discifera, and the structural revision of two sesquiterpenoids from Laggera pterodonta W.-M. ZHU, Q. ZHAO, S.-L. LI and X.-J. HAO Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 4,5-epi-cryptomeridiol C15H26O ÏàËÆ¶È:53.3% Journal of Natural Products 1992 Vol 55 730 Three New Eudesmane Sesquiterpenes from Pluchea arguta Viqar Uddin Ahmad, Tanveer Ahmed Farooqui, Kaniz Fizza, Azra Sultana, Rasheeda Khatoon Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 4,5-epi-cryptomeridiol ÏàËÆ¶È:53.3% Journal of Natural Products 1994 Vol 57 1189 Synthetic Studies of Sesquiterpenes with a cis-Fused Decalin System, 4. Synthesis of (+)-5¦ÂH-Eudesma-3,11-diene, (-)-5¦ÂH-Eudesmane-4¦Â,11-diol, and (+)-5¦ÂH-Eudesmane-4¦Á,11-diol, and Structure Revision of a Natural Eudesmane-4,11-diol Isolated from Pluchea Masayoshi Ando, Koji Arai, Kazuhira Kikuchi, Koji Isogai Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 4¦Â,11-dihydroxy-10-epi-eudesmane C15H26O ÏàËÆ¶È:53.3% Phytochemistry 1992 31 863-880 Sesquiterpene lactones and other constituents from Ursinia species J. Jakupovic, U. Ganzer, P. Pritschow, L. Lehmann, F. Bohlmann, R.M. King Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . 4¦Â,11-¶þôÇ»ù-¶ÔÓ³èñÍé C15H28O2 ÏàËÆ¶È:53.3% Chinese Pharmaceutical Journal 1995 30 264-265 Chemical study on Laggera pterodonta Zhao Aihua, Zhu Yan, Wei Junxian Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . compound X ÏàËÆ¶È:53.3% Heterocycles 2001 54 765-776 Intramolecular Photocycloaddition of 2-Cycloalkenyl-1,3-dioxin-4-one. Stereoselective Synthesis of cis-Eudesmane-4,11-diols Toshihide Hatsui,* Ka Li, Akira Mori,* and Hitoshi Takeshita Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 7-methoxy-1,7-dimethyltricyclo[6.2.2.0(4,9)]dodecan-3-one C15H24O2 ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2006 2006 3181-3192 Towards the Total Synthesis of Vibsanin E, 15-O-Methylcyclovibsanin B,3-Hydroxyvibsanin E, Furanovibsanin A, and 3-O-Methylfuranovibsanin A Brett D. Schwartz, David P. Tilly, Ralf Heim, Stefan Wiedemann, Craig M. Williams and Paul V. Bernhardt Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 4,10-epoxy-6¦Á-hydroxyguaiane ÏàËÆ¶È:53.3% Zeitschrift f¨¹r Naturforschung C 2012 67 266-274 Isolation of New Cytotoxic Metabolites from Cleome droserifolia Growing in Egypt Shahira M. Ezzat and Amira Abdel Motaal Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound 8 ÏàËÆ¶È:53.3% The Journal of Organic Chemistry 1983 48 4410-4413 An aristolane sesquiterpenoid from the sea pen Scytalium splendens Muu N. Do, Karen L. Erickson Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . pterodondiol C15H28O2 ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2014 50 732-734 Chemical Components of the Fibrous Root of Ophiopogon japonicus Tian Feng, Shen Lan, Wang ChenJie, Feng Yi, Zheng XiangWei Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . chrysothol monoacetyl derivative(1b) ÏàËÆ¶È:52.9% Phytochemistry 2006 67 1547-1553 Constituents of Chrysothamnus viscidiflorus Ahmed A. Ahmed , Mohamed-Elamir F. Hegazy, Nahed M. Hassan,Malgorzata Wojcinska, Joe Karchesy, Paul W. Pare, Tom J. Mabry Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . rel- (1R,2R,3R,4S,6S)-p-menthane-1,2,3,6-tetrol C10H20O4 ÏàËÆ¶È:50% Helvetica Chimica Acta 2006 Vol. 89 558 Terpenoids from Eupatorium fortunei TURCZ Hai-Xia Jiang, Ya Li, Jing Pan, and Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . (1R,2R)-p-menth-3-ene-1,2-diol C10H18O2 ÏàËÆ¶È:50% Phytochemistry 2004 65 3279-3287 Monoterpenoids and their glycosides from the leaf of thyme Junichi Kitajima, Toru Ishikawa, Atushi Urabe, Mitsuru Satoh Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . pandangolide 1a C12H20O5 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 1350-1353 Pandangolide 1a, a Metabolite of the Sponge-Associated Fungus Cladosporium sp., and the Absolute Stereochemistry of Pandangolide 1 and iso-Cladospolide B Shiri Gesner, Naama Cohen, Micha Ilan, Oded Yarden, and Shmuel Carmeli Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . pandangolide 1 C12H20O5 ÏàËÆ¶È:50% Journal of Natural Products 2005 68 1350-1353 Pandangolide 1a, a Metabolite of the Sponge-Associated Fungus Cladosporium sp., and the Absolute Stereochemistry of Pandangolide 1 and iso-Cladospolide B Shiri Gesner, Naama Cohen, Micha Ilan, Oded Yarden, and Shmuel Carmeli Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . pandangolide 4 C24H38O8S ÏàËÆ¶È:50% Journal of Natural Products 2001 64 527-530 New Macrolides and Furan Carboxylic Acid Derivative from the Sponge-Derived Fungus Cladosporium herbarum Raquel Jadulco,Peter Proksch,Victor Wray,Sudarsono,Albrecht Berg,and Udo Gräfe Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . 3-isopropyl-6-methyltricyclo[4.4.0.02,8]decan-7-one ÏàËÆ¶È:50% Journal of Natural Products 2001 64 406-410 A Formal Total Synthesis of Racemic Sesquiterpenoid Sativene Sasan Karimi Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . pandangolide 1 C12H21O5 ÏàËÆ¶È:50% Journal of Natural Products 2000 63 142-145 Novel Polyketide Metabolites from a Species of Marine Fungi Cameron J. Smith,Darren Abbanat, Valerie S. Bernan, William M. Maiese, Michael Greenstein, Jamaluddin Jompa,Akbar Tahir,and Chris M. Ireland Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . cis-4,8-dimethyl-6-nonanolide C11H20O2 ÏàËÆ¶È:50% Journal of Natural Products 1997 60 493-494 A Synthesis of 6-Myoporol Tse-Lok Ho and Rong-Jie Chein Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . cytochalasin P C30H41NO6 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1987 35 902-905 THREE NEW 10-PHENYL- [11] CYTOCHALASANS, CYTOCHALASINS N, O, AND P FROM PHOMOPSIS SP Takako Tomioka,Yoshihiko Izawa,Kiyotaka Koyama and Shinsaku Natori Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . (R)-6-[(acetyloxy)imino]-4-methyl-1-isopropylcyclohex-1-ene C12H19NO2 ÏàËÆ¶È:50% Chemistry of Natural Compounds 2003 39 569-572 (R)-4-MENTHEN-3-ONE anti-OXIME AND ITS TRANSFORMATION UNDER BECKMAN REARRANGEMENT CONDITIONS R. Ya. Kharisov, E. R. Latypova, R. F. Talipov,R. R. Muslukhov, G. Yu. Ishmuratov,and G. A. Tolstikov Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . (1S*,2S*,3S*,4R*,6R*)-1,2,3,6-tetrahydroxy-P-menthane C10H19O4 ÏàËÆ¶È:50% Chinese Chemical Letters 2005 16 1217-1219 Highly Oxygenated Monoterpenes from Eupatorium fortunei Hal Xia¢òANG Kun GAO Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . deoxyoleanolic acid ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 1989 14 32-33 Studies on the Chemical Constituents of Schizonepeta mulifida(L.)Briq Zang Youwei, Ma Bingru Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . (E )-7¦ÁH-germacra-1(10),4(15)-diene-5¦Á,6¦Â-diol C15H26O2 ÏàËÆ¶È:50% Phytochemistry 1999 51 529-541 Bioactive sesquiterpenes from Santolina rosmarinifolia subsp. Canescens. A conformational analysis of the germacrane ring Alejandro F. Barrero, M. Mar Herrador, Jose F.Quilez, Ramon Alvarez-Manzaneda, Dolores Portal, Jose A. Gavin, Dolores G. Gravalos, M.S.J. Simmonds, W.M. Blaney Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . 1-hydroxy-2,2,6-trimethylbicyclo[4.2.2]dec-9-en-7-on ÏàËÆ¶È:50% Helvetica Chimica Acta 1976 59 1-13 Die Thermolyse von 2,2,6,7-Tetramethyl-1,7-epidioxybicyclo[4.3.O]non-8-en von Werner Skorianetz und Gunther Ohloff Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 2-Methyl-2-(5,5-dimethyl-2-oxo-1,3,2-dioxaphosphinan-2-yl)pyrrolidine C10H20NO3P ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 2218-2230 CyDEPMPOs: A class of stable cyclic DEPMPO derivatives with improved properties as mechanistic markers of stereoselective hydroxyl radical adduct formation in biological systems Gaëlle Gosset, Jean-Louis Cl¨¦ment, Marcel Culcasi, Antal Rockenbauer, Sylvia Pietri Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . 2-Methyl-2-(5,5-diethyl-2-oxo-1,3,2-dioxaphosphinan-2-yl)-3,4-dihydro-2H-pyrrole 1-oxide [Et2CyDEPMPO] C12H22NO4P ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 2218-2230 CyDEPMPOs: A class of stable cyclic DEPMPO derivatives with improved properties as mechanistic markers of stereoselective hydroxyl radical adduct formation in biological systems Gaëlle Gosset, Jean-Louis Cl¨¦ment, Marcel Culcasi, Antal Rockenbauer, Sylvia Pietri Structure 13C NMR ̼Æ×Ä£Äâͼ |

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µÚÒ»¸ö È«²¿ÈܼÁ ²éѯ½á¹û£º¹²²éµ½19¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . trimethyl citrate ÏàËÆ¶È:66.6% China Journal of Chinese Materia Medica 2008 33 1272-1274 Studies on chemical constituents of Dioscorea opposita BAI Bing, LI Mingjing, WANG Yong, LIU Xiuhua Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ÄûÃÊËáÈý¼×õ¥ C9H14O7 ÏàËÆ¶È:66.6% Chinese Traditional and Herbal Drugs 1995 26 105-106 ÎÚ÷µÄ»¯Ñ§³É·ÖÑо¿ Éòºì÷,Ò×Ñ,ÇÇ´«×¿,ËÕÖÐÎä,Àî³Ðìï Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . trimethylcitrate ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 2006 54(12) 1720-1721 A New Citryl Glycoside from Gastrodia elata and Its Inhibitory Activity on GABA Transaminase Jung-Hyun CHOI and Dong-Ung LEE Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 1-(2H-tetrazol-5-yl)-(zinc-1,4,7,10-tetraazacyclododecane)bisperchlorate C9H20N8 ÏàËÆ¶È:60% Heterocycles 2007 74 913-925 Synthesis and Characterization of 1-(2H-Tetrazol-5-yl)-1, 4, 7, 10-tetraazacyclododecane and Its Zn(II), Ni(II) and Cu(II) Complexes Kristina Woinaroschy, Andrei Ursu, and Burkhard König Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-ôÇ»ù-3-ôÈ»ùÎì¶þËá¶þ¼×õ¥ C8H12O7 ÏàËÆ¶È:60% Chinese Traditional and Herbal Drugs 1995 26 105-106 ÎÚ÷µÄ»¯Ñ§³É·ÖÑо¿ Éòºì÷,Ò×Ñ,ÇÇ´«×¿,ËÕÖÐÎä,Àî³Ðìï Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 1,5-dimethyl citrate ÏàËÆ¶È:60% Journal of Shenyang Pharmaceutical University 2009 26 807-810 Isolation and identification of chemical constituents from the fruit and calyx of Physalis alkekengi L. var. franchetii(Mast.)Makino CAI Qian, LIU Yu-qiang, MA Zhe Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1,5-dimethyl citrate ÏàËÆ¶È:60% Natural Product Research and Development 2009 21 731-732 Studies on the Metabolites of Aspergillus aculeatus YM 311498,an Endophytic Fungus from Azadirachta indica A.Juss WU Shao-hua; CHEN You-wei; SHAO Shi-cheng; LI Zhi-ying; YANG Li-yuan; LI Shao-lan Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 1,5-dimethyl citrate C8H12O7 ÏàËÆ¶È:60% Natural Product Research and Development 2004 16 129-130 STUDIES ON THE CHEMICAL CONSTITUENTS OF EMBELIA LAETA TANG Tian-jun;WU Feng-e Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . dimethyl 3-carboxyl-3-hydroxy pentanedioate ÏàËÆ¶È:60% Journal of Chinese Medicinal Materials 2003 26 867-869 Studies on Constituents of Rosa bracteata Fruits(¢ò) Xu Zhiguo, Huang Song, Du Fanglu, Peng Caiyun, Tian Yuwang Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-hydroxy-3-methoxycarbonyl pentanedioic acid ÏàËÆ¶È:60% Journal of Chinese Medicinal Materials 2003 26 867-869 Studies on Constituents of Rosa bracteata Fruits(¢ò) Xu Zhiguo, Huang Song, Du Fanglu, Peng Caiyun, Tian Yuwang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 1 C18H22N2O6S2 ÏàËÆ¶È:50% Heterocycles 2009 79 471-486 Subtle Control in Solution and Crystal Structures with Weak Hydrogen Bonds: the Unusual Profile of Dimethyl 3, 12-Dioxo-7, 8 Dithia 4, 11-Diazabicyclo[12.2.2]octadeca-1(16), 14, 17-triene 5, 10-Dicarboxylate (TDA1) Isabella L. Karle, Lulu Huang, Punna Venkateshwarlu, A. V. S. Sarma, and Subramania Ranganathan Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 4,5-diazahexacyclo[6.4.1.02,7.03,11.06,10.09,12]tridec-4-ene C11H12N2 ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 7573-7575 Carbenes in polycyclic systems. Generation and fate of pentacyclo[5.4.0.02,6.03,10.55,9]undecanylidene species Jelena Veljković, Lada Klaić, Kata Mlinarić-Majerski Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 11 C16H20O9 ÏàËÆ¶È:50% Tetrahedron Letters 2004 45 3397-3399 An easy way for constructing hard-to-make epoxides employing HOF¡¤CH3CN Elizabeth Golan, Aviv Hagooly, Shlomo Rozen Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . trimethyl citrate ÏàËÆ¶È:50% Journal of Shenyang Pharmaceutical University 2008 25 705-707 Chemical constituents of water-soluble part of Mentha spicata L. SONG Yan, CHEN Guang-tong, SUN Bo-hang, HUANG Jian, LI Xian, WU Li-jun Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . citric acid C6H8O7 ÏàËÆ¶È:50% Journal of China Pharmaceutical University 2005 36 520-522 Chemical Constituents of Evodia rutaecarpa WANG Qi-Zhi; LIANG Jing-Yu; CHEN Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . Me2-Aeg(me)-OH¡¤ 2 HCl ÏàËÆ¶È:50% Helvetica Chimica Acta 2011 94 1952-1980 Improved Large-Scale Liquid-Phase Synthesis and High-Temperature NMR Characterization of Short -(F-)PNAs (pages 1952¨C1980) Tobias A. Plöger and G¨¹nter von Kiedrowski Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . trimethyl citrate ÏàËÆ¶È:50% Journal of Chinese Medicinal Materials 2003 26 867-869 Studies on Constituents of Rosa bracteata Fruits(¢ò) Xu Zhiguo, Huang Song, Du Fanglu, Peng Caiyun, Tian Yuwang Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 2-exo-4-exodibromobicyclo[3.2.1]octane ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 1996 34 131-136 NMR Study of Substituted Bicyclo[3.2.1]octanes John W. Blunt, Andrew Burritt, James M. Coxon and Peter J. Steel Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . trimethyl citrate ÏàËÆ¶È:50% Chinese Joumal of Experimental Traditional Medical Fomulae 2012 18 110-112 Chemical Constituents from the Fruits of Vatica mangachapoi LIN Hai, LI Wen, RONG Sui-hua Structure 13C NMR ̼Æ×Ä£Äâͼ |

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