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20071070088Ìú³æ (СÓÐÃûÆø)
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CÆ×Êý¾ÝÈçÏ£º 13C NMR (101 MHz, Pyr) ¦Ä£º 12.57,14.73,15.98,21.13,22.42,22.57,22.91,23.23,33.24,33.39,37.97,39.56,40.91,49.94,52.22,52.65,54.63,79.05,79.95,111.32,113.50,121.64,128.98,129.88,139.24,142.66,144.12,161.25,165.24,167.11,172.99,174.48,214.70 |
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20071070088: ½ð±Ò+10, ¡ïÓаïÖú 2013-08-28 10:30:19
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20071070088: ½ð±Ò+10, ¡ïÓаïÖú 2013-08-28 10:30:19
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²éѯ½á¹û£º¹²²éµ½75¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . tigloylseneganolide A C32H38O8 ÏàËÆ¶È:81.8% Journal of Natural Products 2007 70 1344-1347 Tetranortriterpenoids from Cipadessa baccifera Li-She Gan, Xiao-Ning Wang, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Erythrocarpine A C34H38O8 ÏàËÆ¶È:67.6% Bioorganic & Medicinal Chemistry 2007 15 5997-6002 Erythrocarpines A¨CE, new cytotoxic limonoids from Chisocheton erythrocarpus Khalijah Awang, Chong Soon Lim, Khalit Mohamad, Hiroshi Morita, Yusuke Hirasawa, Koichi Takeya, Odile Thoison, A. Hamid A. Hadi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . swietmanin I C32H38O9 ÏàËÆ¶È:66.6% Journal of Natural Products 2009 72 2084-2090 Structurally Diverse Limonoids from the Fruits of Swietenia mahagoni Bing-Dong Lin, Tao Yuan, Chuan-Rui Zhang, Lei Dong, Bo Zhang, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . granatumin A C31H36O8 ÏàËÆ¶È:66.6% Journal of Natural Products 2009 72 2110-2114 Granatumins A-G, Limonoids from the Seeds of a Krishna Mangrove, Xylocarpus granatum Min-Yi Li, Xiao-Bo Yang, Jian-Yu Pan, Gang Feng, Qiang Xiao, Jari Sinkkonen, Tirumani Satyanandamurty, and Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . granatumin B C32H40O8 ÏàËÆ¶È:63.6% Journal of Natural Products 2009 72 2110-2114 Granatumins A-G, Limonoids from the Seeds of a Krishna Mangrove, Xylocarpus granatum Min-Yi Li, Xiao-Bo Yang, Jian-Yu Pan, Gang Feng, Qiang Xiao, Jari Sinkkonen, Tirumani Satyanandamurty, and Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . granatumin C C32H38O9 ÏàËÆ¶È:63.6% Journal of Natural Products 2009 72 2110-2114 Granatumins A-G, Limonoids from the Seeds of a Krishna Mangrove, Xylocarpus granatum Min-Yi Li, Xiao-Bo Yang, Jian-Yu Pan, Gang Feng, Qiang Xiao, Jari Sinkkonen, Tirumani Satyanandamurty, and Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . ¦¤8¨C30,14¨C153¦Â-acetoxy-1-oxo-methylmeliacate ÏàËÆ¶È:63.6% Natural Product Research 2008 22 763-800 13C NMR spectroscopy of D and B, D-ring seco-limonoids of Meliaceae family T. Narender; T. Khaliq; Shweta Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 30¦Á-hydroxyl xylogranatin A C32H40O10 ÏàËÆ¶È:63.6% Zeitschrift f¨¹r Naturforschung B 2007 62b 859-862 Two New Limonoids with a 3-O-¦Â-Tigloyl Group from the Seeds of the Chinese Mangrove Xylocarpus granatum Jun Wu, Minyi Li, Si Zhang, QiangXiao, and Qingxin Li Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 3¦Â-acetoxy-1-oxo-¡÷8(10),14(15) methyl meliacate ÏàËÆ¶È:63.6% Journal of the Chemical Society, Perkin Transactions 1 1974 437-441 13 C nuclear magnetic resonance spectra of some limonoids. Part I. The structure of procerin, an extractive from Carapa procera David A. H. Taylor Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . xylogranatin A C32H40O9 ÏàËÆ¶È:60.6% Chemical & Pharmaceutical Bulletin 2006 54(11) 1582-1585 Xylogranatins A¡ªD, New Mexicanolides from the Fruit of a Chinese Mangrove Xylocarpus granatum Jun WU,Si ZHANG,Minyi LI,Yuan ZHOU,and Qiang XIAO Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . khayasin T C32H40O8 ÏàËÆ¶È:60.6% Chemical & Pharmaceutical Bulletin 1990 38 639-651 Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . xylomexicanolide A C31H38O8 ÏàËÆ¶È:60.6% Chemical & Pharmaceutical Bulletin 2010 58 552-555 Mexicanolides from the Seeds of a Krishna Mangrove, Xylocarpus moluccensis Jing Zhang, Sheng-Xin Yang, Xiao-Bo Yang, Min-Yi Li, Gang Feng, Jian-Yu Pan, Tirumani Satyanandamurty and Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . xylocarpins B C32H42O9 ÏàËÆ¶È:60.6% Magnetic Resonance in Chemistry 2007 45 705-709 Xylocarpins A and B, two new mexicanolides from the seeds of a Chinese mangrove Xylocarpus granatum: NMR investigation in mixture (pages 705¨C709) Minyi Li, Jun Wu, Si Zhang, Qiang Xiao and Qingxin Li Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . indiangranatumin A ÏàËÆ¶È:60.6% Chinese Traditional and Herbal Drugs 2010 41 846-851 Chemical constituents in seeds of Indian mangrove Xylocarpus granatum YANG Xiao-bo; YANG Sheng-xin; LI Min-yi; PAN Jian-yu; ZHENG Yi-nan; WU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . khayasin T ÏàËÆ¶È:60.6% Chinese Traditional and Herbal Drugs 2010 41 846-851 Chemical constituents in seeds of Indian mangrove Xylocarpus granatum YANG Xiao-bo; YANG Sheng-xin; LI Min-yi; PAN Jian-yu; ZHENG Yi-nan; WU Jun Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . xylogodavarin D C32H38O8 ÏàËÆ¶È:57.5% Chemistry-A European Journal 2012 18 14342-14351 Andhraxylocarpins A¨CE: Structurally Intriguing Limonoids from the True Mangroves Xylocarpus granatum and Xylocarpus moluccensis Jun Li, Dr. Min-Yi Li, Dr. Torsten Bruhn, Dr. Daniel C. G. Götz, Prof. Dr. Qiang Xiao, Tirumani Satyanandamurty, Prof. Dr. Jun Wu and Prof. Dr. Gerhard Bringmann Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 7 C34H52O7 ÏàËÆ¶È:55.8% Chinese Journal of Chemistry 1987 5 154-161 Studies on the chemical constituents of Ilex pubescens Hook et Arn: II. The structure of Ilexsaponin A Qin Guo-Wei, Chen Zheng-Xiong, Xu Ren-Sheng, Jiang Zhong-Fang and Liang Jing-Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Andirolide D C34H42O11 ÏàËÆ¶È:55.8% Tetrahedron 2011 67 782-792 Absolute stereostructure of Andirolides A¨CG from the flower of Carapa guianensis (Meliaceae) Yuji Tanaka, Takeshi Yamada, Yasuko In, Osamu Muraoka, Tetsuya Kajimoto, Reiko Tanaka Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 7 ÏàËÆ¶È:55.8% Acta Chimica Sinica 1987 45 249-255 Studies on the Chemical Constituents of Ilex pubescens Hook et Am II. The Structure of Ilexsaponin A Qin Guo-Wei Chen Zheng-Xiong Xu Ren-ShengJiang Zhong-Fang Liang Jing-Guo Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . swietmanin H C29H34O9 ÏàËÆ¶È:54.5% Journal of Natural Products 2009 72 2084-2090 Structurally Diverse Limonoids from the Fruits of Swietenia mahagoni Bing-Dong Lin, Tao Yuan, Chuan-Rui Zhang, Lei Dong, Bo Zhang, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . quivisianone C33H42O11 ÏàËÆ¶È:54.5% Phytochemistry 2005 66 1100-1107 Mexicanolide limonoids from the Madagascan Meliaceae Quivisia papinae Philip H. Coombes , Dulcie A. Mulholland, Milijaona Randrianarivelojosia Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . swietemahonin E C32H40O10 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 1990 38 894-901 Constitutents of the Seeds of Swietenia mahagoni JACQ.II. : Structures of Swietemahonin A, B, C, D, E, F, and G and Swietemahonolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . methyl 3¦Â-tigloyloxy-2-hydroxy-1-oxo-meliac-8(30)-enate C32H40O9 ÏàËÆ¶È:54.5% Chemical & Pharmaceutical Bulletin 1998 46 523-525 Tetranortriterpenoids from Swietenia macrophylla Keisuke KOJIMA,Kimio ISAKA and Yukio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . methyl-2-hydroxy-3¦Â-tigloyloxy-1-oxomeliac-8(30)-enate ÏàËÆ¶È:54.5% Phytochemistry 1998 49 1981-1988 Limonoids from Swietenia humilis and Guarea grandiflora (Meliaceae)Taken in part from the PhD and MS theses of C. Villarreal and M. A. Jim¨¦nez, respectively. Adelina Jimenez, Claudina Villarreal, Ruben Alfredo Toscano, Mathew Cook, John T. Arnason, Robert Bye, Rachel Mata Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . xylomexicanin B C32H42O9 ÏàËÆ¶È:54.5% Zeitschrift f¨¹r Naturforschung C 2009 64 37-42 Xylomexicanins A and B, New D14,15-Mexicanolides from Seeds of the Chinese Mangrove Xylocarpus granatum L.-R. Shen, M. Dong, D. Guo, B.-W. Yin, M.-L. Zhang, Q.-W. Shi, C.-H. Huo, H. Kiyota, N. Suzuki, and B. Cong Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . moluccensin U C32H40O10 ÏàËÆ¶È:54.5% Journal of Natural Products 2012 75 1277-1283 Moluccensins R¨CY, Limonoids from the Seeds of a Mangrove, Xylocarpus moluccensis Jun Li, Min-Yi Li, Gang Feng, Jing Zhang, Maarit Karonen, Jari Sinkkonen, Tirumani Satyanandamurty, and Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . ∆8,14-2-hydroxy-6-deoxyswietenine ÏàËÆ¶È:54.5% European Journal of Organic Chemistry 2010 1455-1459 Asymmetric Cyanosilylation of -Keto Esters Catalyzed by the [Ru(phgly)2(binap)]¨CC6H5OLi System Nobuhito Kurono, Masato Uemura and Takeshi Ohkuma Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . xylogodavarin A C32H38O9 ÏàËÆ¶È:54.5% Chemistry-A European Journal 2012 18 14342-14351 Andhraxylocarpins A¨CE: Structurally Intriguing Limonoids from the True Mangroves Xylocarpus granatum and Xylocarpus moluccensis Jun Li, Dr. Min-Yi Li, Dr. Torsten Bruhn, Dr. Daniel C. G. Götz, Prof. Dr. Qiang Xiao, Tirumani Satyanandamurty, Prof. Dr. Jun Wu and Prof. Dr. Gerhard Bringmann Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . chisomicine A C32H38O8 ÏàËÆ¶È:54.5% Journal of Natural Products 2011 74 1313-1317 Chisomicines A−C, Limonoids from Chisocheton ceramicus Ibrahim A. Najmuldeen, A. Hamid A. Hadi, Khalijah Awang, Khalit Mohamad, Kamal Aziz Ketuly, Mat Ropi Mukhtar, Soon-Lim Chong, Gomathi Chan, Mohd Azlan Nafiah, Ng Seik Weng, Osamu Shirota, Takahiro Hosoya, Alfarius E. Nugroho, and Hiroshi Morita Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 3-O-tigloyl-6-O-acetylswietenolide C34H42O10 ÏàËÆ¶È:52.9% Chemical & Pharmaceutical Bulletin 1990 38 639-651 Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . humilinolide C C34H42O10 ÏàËÆ¶È:52.9% Journal of Natural Products 1993 Vol 56 1567-1574 New Tetranortriterpenoids from Swietenia humilis Rosabel Segura-Correa, Rachel Mata, Ana Luisa Anaya, Blanca Hernandez-Bautista, Rene Villena, Manuel Soriano-Garcia, Robert Bye, Edelmira Linares Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 3-O-tigloyl-6-O-acetyl-swietenolide ÏàËÆ¶È:52.9% Journal of Natural Products 1994 Vol 57 1446 Structures of a New Limonoid and a New Triterpenoid Derivative from Pericarps of Trichilia connaroides Akira Inada, Mari Konishi, Hiroko Murata, Tsutomu Nakanishi Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 6-O-acetylswietemahonin G C34H42O12 ÏàËÆ¶È:52.9% Heterocycles 2004 63 389-399 Three New Mexicanolides from the Stem Bark of Swietenia mahogani Jacq. Mona M. G. Saad, Tetsuo Iwagawa, Hiroaki Okamura, Matsumi Doe, and Munehiro Nakatani* Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . Urs-3b-O-cinnamoyl-12-en ÏàËÆ¶È:52.9% Journal of the Brazilian Chemical Society 1998 9 430-434 Chemical Constituents from Himatanthus articulata. Alaide de S¨¢ Barreto, M¨¢rio Geraldo de Carvalho, Ivanilton de Almeida Nery, Luiz Gonzaga, and Maria Auxiliadora Coelho Kaplan Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . compound 20 C36H58O6 ÏàËÆ¶È:52.7% Tetrahedron 2005 61 10569-10582 Triterpenoids from Cedrela sinensis Kumiko Mitsui, Masato Maejima, Hiroaki Saito, Haruhiko Fukaya, Yukio Hitotsuyanagi, Koichi Takeya Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . cineracipadesin D C31H40O10 ÏàËÆ¶È:51.5% Journal of Natural Products 2009 72 714-718 Tetranortriterpenoids from the Leaves of Cipadessa cinerascens Xin Fang, Ying-Tong Di, Chun-Shun Li, Zhao-Liang Geng, Zhen Zhang, Yu Zhang,Yang Lu, Qi-Tai Zheng,Shi-Yin Yang,and Xiao-Jiang Hao Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . baimantuoluoline A C28H38O7 ÏàËÆ¶È:51.5% Helvetica Chimica Acta 2007 Vol. 90 1522 Withanolide Compounds from the Flower of Datura metel L. Bingyou Yang, Qiuhong Wang, Yonggang Xia, Weisheng Feng, and Haixue Kuang Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . swietmanin G C31H38O9 ÏàËÆ¶È:51.5% Journal of Natural Products 2009 72 2084-2090 Structurally Diverse Limonoids from the Fruits of Swietenia mahagoni Bing-Dong Lin, Tao Yuan, Chuan-Rui Zhang, Lei Dong, Bo Zhang, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . granatumin D C32H42O8 ÏàËÆ¶È:51.5% Journal of Natural Products 2009 72 2110-2114 Granatumins A-G, Limonoids from the Seeds of a Krishna Mangrove, Xylocarpus granatum Min-Yi Li, Xiao-Bo Yang, Jian-Yu Pan, Gang Feng, Qiang Xiao, Jari Sinkkonen, Tirumani Satyanandamurty, and Jun Wu Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . (Z)-sarcodictyin A C28H36N2O6 ÏàËÆ¶È:51.5% Journal of Natural Products 2003 66 524-527 (Z)-Sarcodictyin A, a New Highly Cytotoxic Diterpenoid from the Soft Coral Bellonella albiflora Yoichi Nakao, Satoru Yoshida, Shigeki Matsunaga, and Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . xylocarpin B C33H42O12 ÏàËÆ¶È:51.5% Journal of Natural Products 2007 70 772-778 Xylocarpins A-I, Limonoids from the Chinese Mangrove Plant Xylocarpus granatum Jianxin Cui,Jun Wu,Zhiwei Deng, Peter Proksch,and Wenhan Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . 3-O-tigloylswietenolide C32H40O9 ÏàËÆ¶È:51.5% Chemical & Pharmaceutical Bulletin 1990 38 639-651 Constituents of the Seeds of Swietenia mahagoni JACQ. I. : Isolation, Structures, and 1H- and 13C-Nuclear Magnetic Resonance Signal Assignments of New Tetranortriterpenoids Related to Swietenine and Swietenolide Shigetoshi KADOTA,Lamek MARPAUNG,Tohru KIKUCHI and Hisao EKIMOTO Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . 1' ,4' ,16,17-Tetrahydro-3¦Â-acetoxy-1' -acetyl-6' -methoxy-4' -methyl-(16¦Á,17¦Á)-androsta-5,16-dieno[17,16-b]quinoline C32H43NO4 ÏàËÆ¶È:51.5% Steroids 2004 69 301-312 Synthesis of novel steroid-tetrahydroquinoline hybrid molecules and -homosteroids by intramolecular cyclization reactions Ang¨¦la Magyar, J¨¢nos Wölfling, Melanie Kubas, Jose Antonio Cuesta Seijo, Madhumati Sevvana, Regine Herbst-Irmer, P¨¦ter Forg¨®, Gyula Schneider Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . methyl 3¦Â-tigloyloxy-2-hydroxy-8¦Á,30¦Á-epoxy-1-oxo-meliacate C32H40O10 ÏàËÆ¶È:51.5% Chemical & Pharmaceutical Bulletin 1998 46 523-525 Tetranortriterpenoids from Swietenia macrophylla Keisuke KOJIMA,Kimio ISAKA and Yukio OGIHARA Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 6-acetoxyseneganolide A C29H34O9 ÏàËÆ¶È:51.5% Fitoterapia 2004 75 566-572 Antifungal limonoids from the fruits of Khaya senegalensis Samir A.M. Abdelgaleil, Tetsuo Iwagawa, Matsumi Doec, Munehiro Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ |
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