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ÕâÊÇÄãÇóÖúµÄ»¯ºÏÎïÔÚÏàËÆ¶È50%ÒÔÉÏµÄÆ¥ÅäÐÅÏ¢ ²éѯ½á¹û£º¹²²éµ½35¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . N-methyl-2-(2-hydroxybutyl)-6-(2-hydroxypentylpiperidine) ÏàËÆ¶È:61.5% Zeitschrift f¨¹r Naturforschung C 2002 57 81-84 Antinociceptive Activity of the Natural Piperidine Alkaloid Hydrochlorides from Syphocampylus verticellatus O. G. Miguel, A. R. S. Santos, J. B. Calixto, F. D. Monache, and R. A. Yunes Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 1¦Á-hydroxy-3-deoxypseudoanisatin C15H22O6 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1999 47 1749-1752 Structures of Novel Sesquiterpenes from the Pericarps of Illicium merrillianum Jian-mei HUANG,Chun-shu YANG,Hai WANG,Qiu-ming WU,Jia-ling WANG and Yoshiyasu FUKUYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . nootkatone-1,10-11,12-diepoxide C15H22O3 ÏàËÆ¶È:60% molecules 2011 16 4775-4785 Biologically Important Eremophilane Sesquiterpenes from Alaska Cedar Heartwood Essential Oil and Their Semi-Synthetic Derivatives Mohammad A. Khasawneh, Yeping Xiong, Javier Peralta-Cruz and Joe J. Karchesy Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (7E)-7-Ethyl-10-hydroxyundec-7-ene-3,6-dione C13H22O3 ÏàËÆ¶È:53.8% Helvetica Chimica Acta 2008 Vol. 91 741 Novel Polyketides Isolated from Streptomyces sp. Jian Li, Chun-Hua Lu, and Yue-Mao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ascleposide B(4a) C13H20O5 ÏàËÆ¶È:53.8% Chemical & Pharmaceutical Bulletin 2000 48(12) 1908-1911 5, 11-Epoxymegastigmanes from the Leaves of Asclepias fruticosa Fumiko ABE and Tatsuo YAMAUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . kinganone C13H19NO2 ÏàËÆ¶È:53.8% Planta Medica 2003 69 1066-1068 A New Indolizinone from Polygonatum kingianum Yi-Fen Wang,Chun-Hua Lu,Guo-Fang Lai,Jian-Xin Cao,Shi-De Luo Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . cucubalactone C13H20O5 ÏàËÆ¶È:53.8% Planta Medica 2002 68 91-94 New Norsesquiterpenoids from Cucubalus baccifer Yong-Xian Cheng,Jun Zhou,Shi-Ming Deng,Ning-Hua Tan Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (3S,4R,5S,7S,8S,9S)-3,8-epoxy-7-hydroxy-4,8-dimethylperhydrocyclopenta[c]pyran ÏàËÆ¶È:53.8% Journal of Natural Products 2010 73 632-638 Iridoids and Lignans from Valeriana jatamansi Sheng Lin, Tao Chen, Xiao-Hua Liu, Yun-Heng Shen, Hui-Liang Li, Lei Shan, Run-Hui Liu, Xi-Ke Xu, Wei-Dong Zhang and Hui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 30 C10H20O2 ÏàËÆ¶È:53.8% Phytochemistry 1991 30 3981-3987 Biotransformation of monoterpenoids, (− - and menthols, terpinolene and carvotanacetone by Aspergillus speciesYoshinori Asakawa, Hironobu Takahashi, Masao Toyota, Yoshiaki Noma Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . cucubalactone C13H20O5 ÏàËÆ¶È:53.8% Chinese Traditional and Herbal Drugs 2009 40 681-683 Chemical constituents in butanol extraction from stems and leaves of Arachis hypogaea HE Jing-jing; XIE Jing; HAN Zhu-zhen; SHAO Yi-ci; QIAN Fu-gang Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-¶¡Ñõ¼×»ù-5,6,7,8-ËÄÇâ-8-ßÅßáÁ¨àºÍª C13H19NO2 ÏàËÆ¶È:53.8% Chinese Traditional and Herbal Drugs 2008 39 825-828 µá»Æ¾«µÄ»¯Ñ§³É·ÖÑо¿(¢ò) ÀîÏþ;À´¹ú·À;ÍõÒ×·Ò;Õű£¹ú;ÂÞÊ¿µÂ Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 22 C12H20O ÏàËÆ¶È:53.8% Tetrahedron Letters 2004 45 6591-6594 Rhodium-catalyzed 1,4-addition of terminal alkynes to vinyl ketones Ronald V. Lerum, John D. Chisholm Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 24 C13H20O4 ÏàËÆ¶È:53.8% Tetrahedron 2012 68 1171-1176 Construction of functionalized B/C/D ring system of C19-diterpenoid alkaloids via intramolecular Diels¨CAlder reaction followed by Wagner¨CMeerwein rearrangement Hang Cheng, Liang Xu, De-Lin Chen, Qiao-Hong Chen, Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 5 C12H24O3S ÏàËÆ¶È:53.8% Tetrahedron 2002 58 6405-6412 Hedathiosulfonic acids A and B, novel thiosulfonic acids from the deep-sea urchin Echinocardium cordatum Masaki Kita, Masami Watanabe, Noboru Takada, Kiyotake Suenaga, Kaoru Yamada, Daisuke Uemura Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . squalestatin U2 ÏàËÆ¶È:53.8% The Journal of Antibiotics 1994 47 740-754 THE SQUALESTATINS, NOVEL INHIBITORS OF SQUALENE SYNTHASE PRODUCED BY A SPECIES OF Phoma V. MINOR METABOLITES WILLIAM M. BLOWS, GRAHAM FOSTER, STEPHEN J. LANE, DAVID NOBLE, JOHN E. PIERCEY, PHILIP J. SIDEBOTTOM, GRAHAM WEBB Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 7 ÏàËÆ¶È:53.8% Journal of the American Chemical Society 2004 126 187-193 Schulzeines A−C, New ¦Á-Glucosidase Inhibitors from the Marine Sponge Penares schulzei1 Kentaro Takada, Taisuke Uehara, Yoichi Nakao, Shigeki Matsunaga, Rob W. M. van Soest, and Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3S-Methyl 2-Butoxycarbonylamino-3-[(3-hydroxy-1-propylpropyl)sulfanyl]propanoate ÏàËÆ¶È:53.8% Journal of Agricultural and Food Chemistry 2008 56 3758-3763 Synthesis of the Individual Diastereomers of the Cysteine Conjugate of 3-Mercaptohexanol (3-MH) Kevin H. Pardon, Sean D. Graney, Dimitra L. Capone, Jan H. Swiegers, Mark A. Sefton and Gordon M. Elsey Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (4S)-3¦Á,14-dihydroxycadin-10(15)-ene C15H26O2 ÏàËÆ¶È:53.3% Phytochemistry 2002 59 479-488 Microbial transformation of cadina-4,10(15)-dien-3-one,aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740 Dwight O. Collins, Peter L.D. Ruddock, Jessica Chiverton de Grasse,William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 4 C15H20BrClO ÏàËÆ¶È:53.3% Chemical Communications 1985 260-261 Rhodolaureol and Rhodolauradiol, Two New Halogenated Tricyclic Sesquiterpenes from a Marine Alga Antonio G. Gonzalez, Julio D. Martin, * Victor S. Martin, Ricardo Perez, Bruce Tagle, and Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 8-epiisolipidiol ÏàËÆ¶È:53.3% Planta Medica 2011 77 380-382 New Guaiane Sesquiterpene Lactones from Ixeris dentata Mi-Ran Cha, Yeon Hee Choi, Chun Whan Choi, Dae Seok Yoo, Young Sup Kim, Sang Un Choi, Young Ho Kim, Shi Yong Ryu Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . compound 17 ÏàËÆ¶È:53.3% Australian Journal of Chemistry 1989 42 1591-1603 Tropical Marine Algae. III. New Sesquiterpenes From Laurencia majuscula (Rhodophyta, Rhodophyceae, Ceramiales, Rhodomelaceae) JC Coll and AD Wright Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Decurrenside E C19H24O8 ÏàËÆ¶È:52.9% Journal of Natural Products 2012 75 88-92 Benzyl Benzoate Glycoside and 3-Deoxy-d-manno-2-octulosonic Acid Derivatives from Solidago decurrens Ken Shiraiwa, Shen Yuan, Ayako Fujiyama, Yosuke Matsuo, Takashi Tanaka, Zhi-Hong Jiang, and Isao Kouno Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . 9-bromo-7-methyltricyclo[5.4.0.02,9]undecan-8-one-3-spiro-1'-cyclopropane C14H19OBr ÏàËÆ¶È:50% Journal of Natural Products 2003 66 520-523 An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene Sasan Karimi, and Paula Tavares Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . 9-bromo-3,3,7-trimethyltricyclo[5.4.0.02,9]undecan-8-one C14H21OBr ÏàËÆ¶È:50% Journal of Natural Products 2003 66 520-523 An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene Sasan Karimi, and Paula Tavares Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . montiporic acid A C14H20O3 ÏàËÆ¶È:50% Journal of Natural Products 1996 59 796-797 Montiporic Acids A and B, Cytotoxic and Antimicrobial Polyacetylene Carboxylic Acids from Eggs of the Scleractinian Coral Montipora digitata Nobuhiro Fusetani, Takeo Toyoda, Naoki Asai, Shigeki Matsunaga, and Tadashi Maruyama Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . incarviditone C16H20O6 ÏàËÆ¶È:50% Chemistry & Biodiversity 2009 6 779-783 Incarviditone: A Novel Cytotoxic Benzofuranone Dimer from Incarvillea delavayi Bureau et Franchet Yu-Qi Chen, Yun-Heng Shen, Yong-Qing Su, Ling-Yi Kong, and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . incarvmarein B C16H24O6 ÏàËÆ¶È:50% Journal of Asian Natural Products Research 2009 11 523-528 Cyclohexyl-ethanol derivatives from the roots of Incarvillea mairei Zheng-Sheng Huangac, Yue-Hu Peic, Yun-Heng Shena, Sheng Lina, Chun-Mei Liua,Min Lud and Wei-Dong Zhangab Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . oblongolide W1 C16H24O4 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 55-59 Oblongolides from the Endophytic Fungus Phomopsis sp. BCC 9789 Taridaporn Bunyapaiboonsri, Seangaroon Yoiprommarat, Prasert Srikitikulchai, Kitlada Srichomthong and Saisamorn Lumyong Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . rengyoside A ÏàËÆ¶È:50% Phytochemistry 1995 39 235-241 Cyclohexylethanoids and related glucosides from Millingtonia hortensis Takeshi Hase, Yuka Kawamoto, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki, Chayan Picheansoonthon Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . compound 15 ÏàËÆ¶È:50% Phytochemistry 1994 35 713-719 Compounds with the labdane skeleton from Halimium viscosum Julio G. Urones, Isidro S. Marcos, Pilar Basabe, David Diez, Narciso M. Garrido, Concepci¨®n Alonso, Isabel M. Oliva, Anna M. Lithgow, Rosalina F. Moro, M Jose Sexmero, Carlos Lopez Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . N-(((1R,2S,4S,5R)-2-(tert-butyldimethylsilyloxy)-5-(hydroxymethyl)-4-methylcyclohexyl)methyl)acetamide C16H33NO4Si ÏàËÆ¶È:50% Organic Letters 2009 Vol.11,No.1 217-220 Total Synthesis and Structural Confirmation of Brevisamide, a New Marine Cyclic Ether Alkaloid from the Dinoflagellate Karenia brevis Takefumi Kuranaga, Tomohiro Shirai, Daniel G. Baden, Jeffrey L. C. Wright,Masayuki Satake, and Kazuo Tachibana Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . compound 15 C16H31NO4 ÏàËÆ¶È:50% Heterocycles 2010 80 395-408 Synthesis of (+)-Batzelladine K Miyuki Sekine, Yumi Iijima, Osamu Iwamoto, and Kazuo Nagasawa Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . (5R,8S,8as)-N-methoxy-N-methyl-5-propyloctahydroindolizine-8-carboxamide ÏàËÆ¶È:50% Heterocycles 2009 79 935-953 Formal Synthesis of (5R,8R,8aS)-Indolizidine 209I via Enaminones Incorporating Weinreb Amides Charles B. de Koning, Joseph P. Michael, and Darren L. Riley Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . tert-Butyl 7-methyl-3-oxoundecanoate ÏàËÆ¶È:50% Bioscience, Biotechnology, and Biochemistry 2010 74 119-124 Improved Synthesis of Three Methyl-Branched Pheromone Components Produced by the Female Lichen Moth Tomonori TAGURI, Rei YAMAKAWA, Yasushi ADACHI, Kenji MORI and Tetsu ANDO Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . Talaperoxide C C14H20O4 ÏàËÆ¶È:50% Journal of Natural Products 2011 74 1230-1235 Cytotoxic Norsesquiterpene Peroxides from the Endophytic Fungus Talaromyces flavus Isolated from the Mangrove Plant Sonneratia apetala Hanxiang Li, Hongbo Huang, Changlun Shao, Huarong Huang, Jieyi Jiang, Xun Zhu, Yayue Liu, Lan Liu, Yongjun Lu, Mengfeng Li, Yongcheng Lin, and Zhigang She Structure 13C NMR ̼Æ×Ä£Äâͼ |
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1 . N-methyl-2-(2-hydroxybutyl)-6-(2-hydroxypentylpiperidine) ÏàËÆ¶È:61.5% Zeitschrift f¨¹r Naturforschung C 2002 57 81-84 Antinociceptive Activity of the Natural Piperidine Alkaloid Hydrochlorides from Syphocampylus verticellatus O. G. Miguel, A. R. S. Santos, J. B. Calixto, F. D. Monache, and R. A. Yunes Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 1¦Á-hydroxy-3-deoxypseudoanisatin C15H22O6 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 1999 47 1749-1752 Structures of Novel Sesquiterpenes from the Pericarps of Illicium merrillianum Jian-mei HUANG,Chun-shu YANG,Hai WANG,Qiu-ming WU,Jia-ling WANG and Yoshiyasu FUKUYAMA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . nootkatone-1,10-11,12-diepoxide C15H22O3 ÏàËÆ¶È:60% molecules 2011 16 4775-4785 Biologically Important Eremophilane Sesquiterpenes from Alaska Cedar Heartwood Essential Oil and Their Semi-Synthetic Derivatives Mohammad A. Khasawneh, Yeping Xiong, Javier Peralta-Cruz and Joe J. Karchesy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (7E)-7-Ethyl-10-hydroxyundec-7-ene-3,6-dione C13H22O3 ÏàËÆ¶È:53.8% Helvetica Chimica Acta 2008 Vol. 91 741 Novel Polyketides Isolated from Streptomyces sp. Jian Li, Chun-Hua Lu, and Yue-Mao Shen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . ascleposide B(4a) C13H20O5 ÏàËÆ¶È:53.8% Chemical & Pharmaceutical Bulletin 2000 48(12) 1908-1911 5, 11-Epoxymegastigmanes from the Leaves of Asclepias fruticosa Fumiko ABE and Tatsuo YAMAUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . kinganone C13H19NO2 ÏàËÆ¶È:53.8% Planta Medica 2003 69 1066-1068 A New Indolizinone from Polygonatum kingianum Yi-Fen Wang,Chun-Hua Lu,Guo-Fang Lai,Jian-Xin Cao,Shi-De Luo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . cucubalactone C13H20O5 ÏàËÆ¶È:53.8% Planta Medica 2002 68 91-94 New Norsesquiterpenoids from Cucubalus baccifer Yong-Xian Cheng,Jun Zhou,Shi-Ming Deng,Ning-Hua Tan Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . (3S,4R,5S,7S,8S,9S)-3,8-epoxy-7-hydroxy-4,8-dimethylperhydrocyclopenta[c]pyran ÏàËÆ¶È:53.8% Journal of Natural Products 2010 73 632-638 Iridoids and Lignans from Valeriana jatamansi Sheng Lin, Tao Chen, Xiao-Hua Liu, Yun-Heng Shen, Hui-Liang Li, Lei Shan, Run-Hui Liu, Xi-Ke Xu, Wei-Dong Zhang and Hui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 30 C10H20O2 ÏàËÆ¶È:53.8% Phytochemistry 1991 30 3981-3987 Biotransformation of monoterpenoids, (− - and menthols, terpinolene and carvotanacetone by Aspergillus speciesYoshinori Asakawa, Hironobu Takahashi, Masao Toyota, Yoshiaki Noma Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . cucubalactone C13H20O5 ÏàËÆ¶È:53.8% Chinese Traditional and Herbal Drugs 2009 40 681-683 Chemical constituents in butanol extraction from stems and leaves of Arachis hypogaea HE Jing-jing; XIE Jing; HAN Zhu-zhen; SHAO Yi-ci; QIAN Fu-gang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 3-¶¡Ñõ¼×»ù-5,6,7,8-ËÄÇâ-8-ßÅßáÁ¨àºÍª C13H19NO2 ÏàËÆ¶È:53.8% Chinese Traditional and Herbal Drugs 2008 39 825-828 µá»Æ¾«µÄ»¯Ñ§³É·ÖÑо¿(¢ò) ÀîÏþ;À´¹ú·À;ÍõÒ×·Ò;Õű£¹ú;ÂÞÊ¿µÂ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . compound 22 C12H20O ÏàËÆ¶È:53.8% Tetrahedron Letters 2004 45 6591-6594 Rhodium-catalyzed 1,4-addition of terminal alkynes to vinyl ketones Ronald V. Lerum, John D. Chisholm Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 24 C13H20O4 ÏàËÆ¶È:53.8% Tetrahedron 2012 68 1171-1176 Construction of functionalized B/C/D ring system of C19-diterpenoid alkaloids via intramolecular Diels¨CAlder reaction followed by Wagner¨CMeerwein rearrangement Hang Cheng, Liang Xu, De-Lin Chen, Qiao-Hong Chen, Feng-Peng Wang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . compound 5 C12H24O3S ÏàËÆ¶È:53.8% Tetrahedron 2002 58 6405-6412 Hedathiosulfonic acids A and B, novel thiosulfonic acids from the deep-sea urchin Echinocardium cordatum Masaki Kita, Masami Watanabe, Noboru Takada, Kiyotake Suenaga, Kaoru Yamada, Daisuke Uemura Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . squalestatin U2 ÏàËÆ¶È:53.8% The Journal of Antibiotics 1994 47 740-754 THE SQUALESTATINS, NOVEL INHIBITORS OF SQUALENE SYNTHASE PRODUCED BY A SPECIES OF Phoma V. MINOR METABOLITES WILLIAM M. BLOWS, GRAHAM FOSTER, STEPHEN J. LANE, DAVID NOBLE, JOHN E. PIERCEY, PHILIP J. SIDEBOTTOM, GRAHAM WEBB Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . compound 7 ÏàËÆ¶È:53.8% Journal of the American Chemical Society 2004 126 187-193 Schulzeines A−C, New ¦Á-Glucosidase Inhibitors from the Marine Sponge Penares schulzei1 Kentaro Takada, Taisuke Uehara, Yoichi Nakao, Shigeki Matsunaga, Rob W. M. van Soest, and Nobuhiro Fusetani Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 3S-Methyl 2-Butoxycarbonylamino-3-[(3-hydroxy-1-propylpropyl)sulfanyl]propanoate ÏàËÆ¶È:53.8% Journal of Agricultural and Food Chemistry 2008 56 3758-3763 Synthesis of the Individual Diastereomers of the Cysteine Conjugate of 3-Mercaptohexanol (3-MH) Kevin H. Pardon, Sean D. Graney, Dimitra L. Capone, Jan H. Swiegers, Mark A. Sefton and Gordon M. Elsey Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (4S)-3¦Á,14-dihydroxycadin-10(15)-ene C15H26O2 ÏàËÆ¶È:53.3% Phytochemistry 2002 59 479-488 Microbial transformation of cadina-4,10(15)-dien-3-one,aromadendr-1(10)-en-9-one and methyl ursolate by Mucor plumbeus ATCC 4740 Dwight O. Collins, Peter L.D. Ruddock, Jessica Chiverton de Grasse,William F. Reynolds, Paul B. Reese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound 4 C15H20BrClO ÏàËÆ¶È:53.3% Chemical Communications 1985 260-261 Rhodolaureol and Rhodolauradiol, Two New Halogenated Tricyclic Sesquiterpenes from a Marine Alga Antonio G. Gonzalez, Julio D. Martin, * Victor S. Martin, Ricardo Perez, Bruce Tagle, and Jon Clardy Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 8-epiisolipidiol ÏàËÆ¶È:53.3% Planta Medica 2011 77 380-382 New Guaiane Sesquiterpene Lactones from Ixeris dentata Mi-Ran Cha, Yeon Hee Choi, Chun Whan Choi, Dae Seok Yoo, Young Sup Kim, Sang Un Choi, Young Ho Kim, Shi Yong Ryu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . compound 17 ÏàËÆ¶È:53.3% Australian Journal of Chemistry 1989 42 1591-1603 Tropical Marine Algae. III. New Sesquiterpenes From Laurencia majuscula (Rhodophyta, Rhodophyceae, Ceramiales, Rhodomelaceae) JC Coll and AD Wright Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . Decurrenside E C19H24O8 ÏàËÆ¶È:52.9% Journal of Natural Products 2012 75 88-92 Benzyl Benzoate Glycoside and 3-Deoxy-d-manno-2-octulosonic Acid Derivatives from Solidago decurrens Ken Shiraiwa, Shen Yuan, Ayako Fujiyama, Yosuke Matsuo, Takashi Tanaka, Zhi-Hong Jiang, and Isao Kouno Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 9-bromo-7-methyltricyclo[5.4.0.02,9]undecan-8-one-3-spiro-1'-cyclopropane C14H19OBr ÏàËÆ¶È:50% Journal of Natural Products 2003 66 520-523 An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene Sasan Karimi, and Paula Tavares Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 9-bromo-3,3,7-trimethyltricyclo[5.4.0.02,9]undecan-8-one C14H21OBr ÏàËÆ¶È:50% Journal of Natural Products 2003 66 520-523 An Efficient Formal Synthesis of the Sesquiterpenoid Longifolene Sasan Karimi, and Paula Tavares Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . montiporic acid A C14H20O3 ÏàËÆ¶È:50% Journal of Natural Products 1996 59 796-797 Montiporic Acids A and B, Cytotoxic and Antimicrobial Polyacetylene Carboxylic Acids from Eggs of the Scleractinian Coral Montipora digitata Nobuhiro Fusetani, Takeo Toyoda, Naoki Asai, Shigeki Matsunaga, and Tadashi Maruyama Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . incarviditone C16H20O6 ÏàËÆ¶È:50% Chemistry & Biodiversity 2009 6 779-783 Incarviditone: A Novel Cytotoxic Benzofuranone Dimer from Incarvillea delavayi Bureau et Franchet Yu-Qi Chen, Yun-Heng Shen, Yong-Qing Su, Ling-Yi Kong, and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . incarvmarein B C16H24O6 ÏàËÆ¶È:50% Journal of Asian Natural Products Research 2009 11 523-528 Cyclohexyl-ethanol derivatives from the roots of Incarvillea mairei Zheng-Sheng Huangac, Yue-Hu Peic, Yun-Heng Shena, Sheng Lina, Chun-Mei Liua,Min Lud and Wei-Dong Zhangab Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . oblongolide W1 C16H24O4 ÏàËÆ¶È:50% Journal of Natural Products 2010 73 55-59 Oblongolides from the Endophytic Fungus Phomopsis sp. BCC 9789 Taridaporn Bunyapaiboonsri, Seangaroon Yoiprommarat, Prasert Srikitikulchai, Kitlada Srichomthong and Saisamorn Lumyong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . rengyoside A ÏàËÆ¶È:50% Phytochemistry 1995 39 235-241 Cyclohexylethanoids and related glucosides from Millingtonia hortensis Takeshi Hase, Yuka Kawamoto, Kazuhiro Ohtani, Ryoji Kasai, Kazuo Yamasaki, Chayan Picheansoonthon Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . compound 15 ÏàËÆ¶È:50% Phytochemistry 1994 35 713-719 Compounds with the labdane skeleton from Halimium viscosum Julio G. Urones, Isidro S. Marcos, Pilar Basabe, David Diez, Narciso M. Garrido, Concepci¨®n Alonso, Isabel M. Oliva, Anna M. Lithgow, Rosalina F. Moro, M Jose Sexmero, Carlos Lopez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . N-(((1R,2S,4S,5R)-2-(tert-butyldimethylsilyloxy)-5-(hydroxymethyl)-4-methylcyclohexyl)methyl)acetamide C16H33NO4Si ÏàËÆ¶È:50% Organic Letters 2009 Vol.11,No.1 217-220 Total Synthesis and Structural Confirmation of Brevisamide, a New Marine Cyclic Ether Alkaloid from the Dinoflagellate Karenia brevis Takefumi Kuranaga, Tomohiro Shirai, Daniel G. Baden, Jeffrey L. C. Wright,Masayuki Satake, and Kazuo Tachibana Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . compound 15 C16H31NO4 ÏàËÆ¶È:50% Heterocycles 2010 80 395-408 Synthesis of (+)-Batzelladine K Miyuki Sekine, Yumi Iijima, Osamu Iwamoto, and Kazuo Nagasawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . (5R,8S,8as)-N-methoxy-N-methyl-5-propyloctahydroindolizine-8-carboxamide ÏàËÆ¶È:50% Heterocycles 2009 79 935-953 Formal Synthesis of (5R,8R,8aS)-Indolizidine 209I via Enaminones Incorporating Weinreb Amides Charles B. de Koning, Joseph P. Michael, and Darren L. Riley Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . tert-Butyl 7-methyl-3-oxoundecanoate ÏàËÆ¶È:50% Bioscience, Biotechnology, and Biochemistry 2010 74 119-124 Improved Synthesis of Three Methyl-Branched Pheromone Components Produced by the Female Lichen Moth Tomonori TAGURI, Rei YAMAKAWA, Yasushi ADACHI, Kenji MORI and Tetsu ANDO Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . Talaperoxide C C14H20O4 ÏàËÆ¶È:50% Journal of Natural Products 2011 74 1230-1235 Cytotoxic Norsesquiterpene Peroxides from the Endophytic Fungus Talaromyces flavus Isolated from the Mangrove Plant Sonneratia apetala Hanxiang Li, Hongbo Huang, Changlun Shao, Huarong Huang, Jieyi Jiang, Xun Zhu, Yayue Liu, Lan Liu, Yongjun Lu, Mengfeng Li, Yongcheng Lin, and Zhigang She Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- |
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- and menthols, terpinolene and carvotanacetone by Aspergillus species