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CDCl3 15.3,17.4,18.1,19.4,21.0,23.4,24.8,25.2,28.9,29.7,36.3,36.6,75.3,77.2,79.6,84.4,111.7,128.5,129.5,129.9,132,4,133.4,133.5,135.1,145.6,151.7,166.4,172.3 |
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²éѯ½á¹û£º¹²²éµ½7304¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4-O-acetyl-5-O-benzoyl-3¦Â-hydroxy-20-deoxyingenol C29H36O6 ÏàËÆ¶È:75.8% Journal of Asian Natural Products Research 2008 10 101-104 A new diterpene from the processed roots of Euphorbia Kansui CHUN-FA LI, JIN-HUI WANG, YUE CONG and XIAN LI Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . kansuiphorin C C29H34O6 ÏàËÆ¶È:75.8% Chinese Traditional and Herbal Drugs 2003 34 489-492 Studies on ingenol-type diterpene esters in root tuber of Euphorbia kansui PAN Qin; MIN Zhi-da Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 4 C45H74O7Si2 ÏàËÆ¶È:73.3% Tetrahedron Letters 2001 42 6001-6005 Progress towards the total synthesis of tedanolide: an efficient assembly of the C1¨CC11 subunit Teck-Peng Loh, Li-Chun Feng Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . dibenzoate of planotriol C29H32O5 ÏàËÆ¶È:72.4% Phytochemistry 1996 43 83-93 Alloaromandendranes, bicyclogermacrane and 2,3-secoalloaromandendranes in cultured cells of the liverwort, Heteroscyphus planus Kensuke Nabeta, Shinchi Ohkubo, Reiko Hozumi, Yukiharu Fukushi, Hiroshi Nakai, Kenji Katoh Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . gnidimacrin ÏàËÆ¶È:72.4% Journal of Natural Products 1985 Vol 48 440-445 Antineoplastic and Piscicidal 1-Alkyldaphnane Orthoesters from Pimelea Species Margaret I. Tyler, Merlin E. H. Howden Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-O-benzoylhinokiol C27H34O3 ÏàËÆ¶È:72.4% Phytochemistry 1992 31 3781-3784 Antimalarial compounds from Hoslundia opposita Hans Achenbach, Reiner Waibel, Mayunga H.H. Nkunya, Hugo Weenen Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . kansuiphorin D C27H30O4 ÏàËÆ¶È:72.4% Chinese Traditional and Herbal Drugs 2012 43 1891-1895 Study on antitumor constituents of Euphorbia lunulata WANG Jue; LI Xiao-fan; XIE Pu; WANG Tie-jie Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 12-O-(tert-Butyldiphenylsilyl)constanolactone A C36H51O4Si ÏàËÆ¶È:70% Journal of the American Chemical Society 1995 117 6224-6233 Cyclopropane-Containing Eicosanoids of Marine Origin. Biomimetic Synthesis of Constanolactones A and B from the Alga Constantinea simplex James D. White, Mark S. Jensen Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . chabrolonaphthoquinone B C29H38O5 ÏàËÆ¶È:68.9% Journal of Natural Products 2005 68 1651-1655 Meroditerpenoids from a Formosan Soft Coral Nephthea chabrolii Jui-Hsin Su, Atallah F. Ahmed, Ping-Jyun Sung, Yang-Chang Wu, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . chabrolobenzoquinone H C29H42O5 ÏàËÆ¶È:68.9% Journal of Natural Products 2005 68 1651-1655 Meroditerpenoids from a Formosan Soft Coral Nephthea chabrolii Jui-Hsin Su, Atallah F. Ahmed, Ping-Jyun Sung, Yang-Chang Wu, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . chabrolohydroxybenzoquinone G C29H44O6 ÏàËÆ¶È:68.9% Journal of Natural Products 2005 68 1651-1655 Meroditerpenoids from a Formosan Soft Coral Nephthea chabrolii Jui-Hsin Su, Atallah F. Ahmed, Ping-Jyun Sung, Yang-Chang Wu, and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 13-dehydroxybaccatin III ÏàËÆ¶È:68.9% Phytochemistry 1998 49 113-125 Taxoids from Cell Cultures of Taxus Chinensis Birgitta Menhard, Wolfgang Eisenreich, Peter J. Hylands, Adelbert Bacher, Meinhart H. Zenk Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 5-deoxyingenol 3-angelate 20-acetate ÏàËÆ¶È:68.9% Phytochemistry 1997 45 563-570 Ingenane and lathyrane diterpenes from the latex of Euphorbia canariensis J. Alberto Marco, Juan F. Sanz-Cervera, Alberto Yuste Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 32 C36H47NO3Si ÏàËÆ¶È:68.9% Heterocycles 2006 70 423-459 Aza-[3+3] Annulations. Part 6. Total Synthesis of Putative (-)-Lepadiformine and (-)-Cylindricine C Jiashi Wang, Jacob J. Swidorski, Nadiya Sydorenko, Richard P. Hsung,* Heather A. Coverdale, Jennifer M. Kuyava, and Jia Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . guyonianin E C31H40O8 ÏàËÆ¶È:68.9% Phytochemistry 2010 71 2046-2051 Sulfur-containing constituents and one 1H-pyrrole-2-carboxylic acid derivative from pineapple [Ananas comosus (L.) Merr.] fruit Zong-Ping Zheng, Jinyu Ma, Ka-Wing Cheng, Jianfei Chao, Qin Zhu, Raymond Chuen-Chung Chang, Ming Zhao, Zhi-Xiu Lin, Mingfu Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 2 C37H46O3Si ÏàËÆ¶È:68.9% Tetrahedron Letters 2002 43 3825-3828 A versatile asymmetric synthesis of highly enantiomerically enriched 12(S)-HETE via a combination of enzymatic and chemical processes Young-Ger Suh, Kyung-Hoon Min, Yong-Sil Lee, Seung-Yong Seo, Seok-Ho Kim, Hyun-Ju Park Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 9 C32H38Au2Cl2FeP2 ÏàËÆ¶È:68.9% Zeitschrift f¨¹r Naturforschung B 2009 64 1413-1422 Synthesis and Characterization of [3]Ferrocenophane-derived P,P-Chelate Ligand Gold Complexes Featuring an Aurophilic Interaction G. L¨¹bbe, C. Nilewski, G. Kehr, R. Fröhlich, and G. Erker Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . p-Tolyl 2-O-tert-butyldiphenylsilyl-3-O-levulinoyl-5,6-Oisopropylidene-1-thio-¦Â-D-galactofuranoside C37H46O7SiS ÏàËÆ¶È:68.9% Tetrahedron 2012 68 3795-3802 Synthesis of tetra- and hexasaccharide fragments corresponding to the O-antigenic polysaccharide of Klebsiella pneumoniae San-Yong Zhu, Jin-Song Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 7a C36H50N2O4SSi ÏàËÆ¶È:68.9% Tetrahedron 2012 68 8994-9003 Enantiodivergent synthesis of (+)- and (− -isolaurepanGonzalo Pazos, Manuel P¨¦rez, Zoila G¨¢ndara, Generosa G¨®mez, Yagamare Fall Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 12-O-(tert-Butyldiphenylsily1)constanolactone B ÏàËÆ¶È:68.9% Journal of the American Chemical Society 1995 117 6224-6233 Cyclopropane-Containing Eicosanoids of Marine Origin. Biomimetic Synthesis of Constanolactones A and B from the Alga Constantinea simplex James D. White, Mark S. Jensen Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-09 15:22:59
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²éѯ½á¹û£º¹²²éµ½281¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . dibenzoate of planotriol C29H32O5 ÏàËÆ¶È:68.9% Phytochemistry 1996 43 83-93 Alloaromandendranes, bicyclogermacrane and 2,3-secoalloaromandendranes in cultured cells of the liverwort, Heteroscyphus planus Kensuke Nabeta, Shinchi Ohkubo, Reiko Hozumi, Yukiharu Fukushi, Hiroshi Nakai, Kenji Katoh Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3-O-benzoylhinokiol C27H34O3 ÏàËÆ¶È:58.6% Phytochemistry 1992 31 3781-3784 Antimalarial compounds from Hoslundia opposita Hans Achenbach, Reiner Waibel, Mayunga H.H. Nkunya, Hugo Weenen Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . Taxezopidine P C31H38O8 ÏàËÆ¶È:58.6% Heterocycles 2007 73 341-348 Taxezopidines O and P, New Taxoids from Taxus cuspidata Haruaki Ishiyama, Yuka Kakuguchi, Eri Arita, and Jun'ichi Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (R)-MTPA ester C22H30O4 ÏàËÆ¶È:58.0% Bioscience, Biotechnology, and Biochemistry 2003 66 655-659 Myrsinoic Acids B, C and F, Anti-inflammatory Compounds from Myrsine seguinii Mitsuru HIROTA, Shintaro MIYAZAKI, Tomomi MINAKUCHI, Tomoko TAKAGI and Hisao SHIBATA Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (S)-MTPA ester C22H30O4 ÏàËÆ¶È:58.0% Bioscience, Biotechnology, and Biochemistry 2003 66 655-659 Myrsinoic Acids B, C and F, Anti-inflammatory Compounds from Myrsine seguinii Mitsuru HIROTA, Shintaro MIYAZAKI, Tomomi MINAKUCHI, Tomoko TAKAGI and Hisao SHIBATA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 63 C36H50O6S2Si ÏàËÆ¶È:56.6% Journal of the American Chemical Society 2006 128 2859-2872 Total Synthesis and Structural Elucidation of Azaspiracid-1. Final Assignment and Total Synthesis of the Correct Structure of Azaspiracid-1 K. C. Nicolaou, Theocharis V. Koftis, Stepan Vyskocil, Goran Petrovic, Wenjun Tang, Michael O. Frederick, David Y.-K. Chen, Yiwei Li, Taotao Ling, and Yoichi M. A. Yamada Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 75 C36H50O6S2Si ÏàËÆ¶È:56.6% Journal of the American Chemical Society 2006 128 2859-2872 Total Synthesis and Structural Elucidation of Azaspiracid-1. Final Assignment and Total Synthesis of the Correct Structure of Azaspiracid-1 K. C. Nicolaou, Theocharis V. Koftis, Stepan Vyskocil, Goran Petrovic, Wenjun Tang, Michael O. Frederick, David Y.-K. Chen, Yiwei Li, Taotao Ling, and Yoichi M. A. Yamada Structure 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2013-09-09 15:25:49














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