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²éѯ½á¹û£º¹²²éµ½120¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . tetrahydrohelenalin ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1987 25 201-202 Carbon-13 NMR spectra of some pseudoguaianolides Guillermo Delgado, Laura Alvarez, Eduardo Huerta, Alfonso Romo de Vivar and Rachel Mata Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 3¦Á,4¦Á-epoxy-5¦ÁH,7¦ÁH,6¦ÂH,11¦ÂH-eudesman-6,12-olide ÏàËÆ¶È:60% Journal of Natural Products 1993 Vol 56 1723 A Short Synthesis of (+)-Colartin and (+)-Arbusculin A from (-)-Santonin Gonzalo Blay, Luz Cardona, Begoña Garcia, Jose R. Pedro Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Â,8¦Á-dihydroxy-4¦Â,5¦Á,11¦Â-H-eudesman-6¦Á,12-olide C15H24O4 ÏàËÆ¶È:60% Journal of Natural Products 1995 Vol 58 1498-1507 Microbial Transformations of 6¦Á- and 6 ¦Â-Eudesmanolides by Rhizopus nigricans Cultures Yolanda Garc¨ªa, Andr¨¦s Garc¨ªa-Granados, Antonio Mart¨ªnez, Andr¨¦s Parra, Francisco Rivas, Jos¨¦ Mar¨ªa Arias Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3¦Â,9¦Á-diacetoxycedran-8¦Á-ol C19H30O5 ÏàËÆ¶È:60% Phytochemistry 1995 39 1081-1084 The biotransformation of 8-epicedrol and some relatives by Cephalosporium aphidicola Estelle Gand, James R. Hanson, Habib Nasir Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Jasonone C12H20O2 ÏàËÆ¶È:60% Zeitschrift f¨¹r Naturforschung B 2007 62b 125-128 Jasonone, a Nor-sesquiterepene from Jasonia montana Abou El-Hamd H. Mohamed Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 11,12-Dihydroxydrimene-15-oic acid C15H24O4 ÏàËÆ¶È:60% Journal of Asian Natural Products Research 2013 15 305-309 Two new sesquiterpenes from cultures of the basidiomycete Agaricus arvensis Jiang-Yuan Zhao, Jian-Hai Ding, Zheng-Hui Li, Ze-Jun Dong, Tao Feng, Hong-Bin Zhang & Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 1-tert-Butyl 3-methyl (3S,5R)-5-[(1,1-dimethyl-2-oxoethyl) amino]piperidine-1,3-dicarboxylate C16H28N2O5 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2013 21 5907-5922 Synthesis and optimization of novel (3S,5R)-5-(2,2-dimethyl-5-oxo-4-phenylpiperazin-1-yl)piperidine-3-carboxamides as orally active renin inhibitors Yutaka Mori, Yasuyuki Ogawa, Akiyoshi Mochizuki, Yuji Nakamura, Teppei Fujimoto, Chie Sugita, Shojiro Miyazaki, Kazuhiko Tamaki, Takahiro Nagayama, Yoko Nagai, Shin-ichi Inoue, Katsuyoshi Chiba, Takahide Nishi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . methyl longipin-9-en-15-oate C16H24O3 ÏàËÆ¶È:56.2% Journal of Natural Products 1994 Vol 57 873 ¦Á-Longipinene Derivatives from Santolina viscosa. A Conformational Analysis of the Cycloheptane Ring A. F. Barrero, M. M. Herrador, J. Molina Molina, J. F. Qu¨ªlez, M. Quir¨®s Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl 12-hydroxylongipin-9-en-15-oate ÏàËÆ¶È:56.2% Journal of Natural Products 1994 Vol 57 873 ¦Á-Longipinene Derivatives from Santolina viscosa. A Conformational Analysis of the Cycloheptane Ring A. F. Barrero, M. M. Herrador, J. Molina Molina, J. F. Qu¨ªlez, M. Quir¨®s Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 6 ÏàËÆ¶È:56.2% Journal of Natural Products 1994 Vol 57 873 ¦Á-Longipinene Derivatives from Santolina viscosa. A Conformational Analysis of the Cycloheptane Ring A. F. Barrero, M. M. Herrador, J. Molina Molina, J. F. Qu¨ªlez, M. Quir¨®s Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 10 ÏàËÆ¶È:56.2% Tetrahedron 2011 67 8348-8352 The total synthesis of (-)-connatusin A, a hirsutane-type sesquiterpene isolated from the fungus Lentinus connatus BCC8996 David J.-Y. D. Bon, Martin G. Banwell , Ian A. Cade, Anthony C. Willis Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 7a ÏàËÆ¶È:56.2% Indian Journal of Chemistry Section B 1985 24B 1208-1214 Proton & Carbon-13 NMR Studies of trans-Clerodane Diterpenoids & Congeners:Stereochemical Implications & Certain Correlations with cis-Clerodanes A S SARMA & A K GAYEN Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 4c C18H23NO2 ÏàËÆ¶È:56.2% Chinese Journal of Organic Chemistry 2013 33 2196-2204 Synthesis and Antibacterial Activity of New Pinanyl Nitrogen-Containing Heterocycles Wei Baisong, Gu Wen, Xu Xu, Yang Yiqin, Wang Shifa Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . ent-16,17,19-trihydroxygibberell-20-oic acid 20,19-lactone C20H30O4 ÏàËÆ¶È:55% Phytochemistry 1993 34 693-696 Bio-transformation of gibberellin 20,19-lactones by Rhizopus stolonifer Braulio M. Fraga, J.Clemente Diaz Gomez, M.Shaiq Ali, James R. Hanson Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . dendronobilin I C15H24O3 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2007 Vol. 90 2386 Nine New Sesquiterpenes from Dendrobium nobile Xue Zhanga)b)c), Hong-Wei Liud), Hao Gaoa)b)c), Hui-Ying Hane), Nai-Li Wangb)e), Hou-Ming Wuf), Xin-Sheng Yaoe), and Zhao Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 25 ÏàËÆ¶È:53.3% Journal of Natural Products 2003 66 344-349 Chemical Transformations on Botryane Skeleton. Effect on the Cytotoxic Activity Jos L. Reino, Rosa Durn-Patrn, Inmaculada Segura, Rosario Hernndez-Galn, Hans H. Riese, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 3,4-epoxy-11¦Á,13-dihydroelemen-12, 8-olide C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Products 2001 64 466-471 Sesquiterpenes and Monoterpenes from the Bark of Inula macrophylla Bao-Ning Su,Yoshihisa Takaishi, Tetsuya Yabuuchi, Takenori Kusumi, Motoo Tori,Shigeru Takaoka,Gisho Honda, Michiho Ito, Yoshio Takeda, Olimjon K. Kodzhimatov, and Ozodbek Ashurmetov Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 8-bromo-3-isopropyl-6-methyltricyclo-[4.4.0.02,8]dec-3-ene-7-one ÏàËÆ¶È:53.3% Journal of Natural Products 2001 64 406-410 A Formal Total Synthesis of Racemic Sesquiterpenoid Sativene Sasan Karimi Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 12 C15H18O3 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 22-30 Guaianolides as Immunomodulators. Synthesis and Biological Activities of Dehydrocostus Lactone, Mokko Lactone, Eremanthin, and Their Derivatives Saori Yuuya, Hisahiro Hagiwara, Toshio Suzuki, Masayoshi Ando, Atsushi Yamada, Kouji Suda, Takao Kataoka, and Kazuo Nagai Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . (4R,5R,8R)-4,5-epoxycaryophyllan-8-ol C14H23O2 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 41-44 Biotransformation of Caryophyllene Oxide by Botrytis cinerea Rosa Duran, Elena Corrales, Rosario Hern¨¢ndez-Gal¨¢n, and Isidro G. Collado Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . epidihydropseudoivalin C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Products 1999 62 920-922 Oxidative Transformations of Guaia-1(10)-en-12, 8-olides into Xanthanolides Mariano Mart¨ªnez-V¨¢zquez, Jorge C¨¢rdenas, Lucas Godoy, Martha Mart¨ªnez-Bahena, Ren¨¦ Miranda, and Manuel Salm¨®n Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . 1¦Â-hydroxy-4¦Á,11¦ÁH-eudesma-5-en-12,8¦Â-olide C15H22O3 ÏàËÆ¶È:53.3% Planta Medica 2003 69 662-666 Sesquiterpenes and Other Constituents from the Aerial Parts of Inula japonica Chao Yang,Chun-Ming Wang,Zhong-Jian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . ¦Â-cyclocostunolide C15H20O2 ÏàËÆ¶È:53.3% Acta Botanica Yunnanica 1997 19(1) 85-91 STUDY ON CHEMICAL CONSTITUENTS OF SAUSSUREA LAPPA Yang Hui,¡¡Xie Jinlun, ¡¡Sun Handong Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . sulfoorientalol b C15H26O5S ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1994 42 2430-2435 Crude Drugs from Aquatic Plants. V. On the Constituents of Alismatis Rhizoma. (3). Stereostructures of Water-Soluble Bioactive Sesquiterpenes, Sulfoorientalols a, b, c, and d, from Chinese Alismatis Rhizoma Masayuki YOSHIKAWA,Shoko YAMAGUCHI,Hisashi MATSUDA,Nobumitsu TANAKA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . sulfoorientalol b C15H26O5S ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1993 41 1194-1196 SULFOORIENTALOLS a, b, c, AND d, FOUR NEW BIOLOGICALLY ACTIVE SESQUITERPENES, FROM ALISMATIS RHIZOMA Masayuki YOSHIKAWA,Youich FUKUDA,Shoko HATAKEYAMA,Nobumitsu TANAKA,Hisashi MATSUDA,Johji YAMAHARA and Nobutoshi MURAKAMI Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . 1,5,5,9-Tetramethylspir0[3.5]nonan-l-ol C13H24O ÏàËÆ¶È:53.3% Helvetica Chimica Acta 1980 63 154-190 Photochemische Reaktionen. 106. Mitteilung. Zur Photochemie tetraalkylsubstituierter ¦Ã-Keto-olefine Jacob Berger, Michikazu Yoshioka, Markus P. Zink, Hans R. Wolf, Oskar Jeger Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . (1S,2S,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-yl-ethanal ÏàËÆ¶È:53.3% Molecules 2009 14 2780-2800 Synthesis and Olfactory Evaluation of Bulky Moiety-Modified Analogues to the Sandalwood Odorant Polysantol® Laura Chapado, Pablo J. Linares-Palomino, Concepci¨®n Bad¨ªa, Sof¨ªa Salido, Manuel Nogueras, Adolfo S¨¢nchez and Joaqu¨ªn Altarejos Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . Kobusone C14H22O2 ÏàËÆ¶È:53.3% Biochemical Systematics and Ecology 2007 35 470-471 Kobusone: Occurrence of a norsesquiterpenoid in the gorgonian coral Rumphella antipathies (Gorgoniidae) Li-Fan Chuang, Tung-Yung Fan, Jan-Jung Li, Ping-Jyun Sung Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . 3¦Á,11¦Â-dihydroxy-1,2,4¦Â,5¦Á,6¦Â-H-eudesman-6,12-olide C15H24O4 ÏàËÆ¶È:53.3% Natural Product Research 2008 22 499-506 Biotransformation of tetrahydro-¦Á-santonins by Absidia coerulea Lin Yang; Jungui Dai Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . diversifolide C13H20O3 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 1999 47 428-429 A New Dinorxanthane and Chromone from the Root of Tithonia diversifolia Yueh-Hsiung KUO and Ben-Yan LIN Structure 13C NMR ̼Æ×Ä£Äâͼ 31 . 1¦Á-hydroxycolartin or 1¦Á,4¦Á-dihydroxyeudesman-5¦Á,6¦Â,7¦Á,11bH-12,6-olide C15H24O4 ÏàËÆ¶È:53.3% Phytochemistry 1999 51 995-997 Minor eudesmanolides from Artemisia canariensis Horacio Mansilla, J. Antonio Palenzuela Structure 13C NMR ̼Æ×Ä£Äâͼ 32 . 5¦Â-hydroxy-4,9-oxidogermacr-11¦Á-H,13-6,12-olide C15H24O4 ÏàËÆ¶È:53.3% Phytochemistry 1994 37 1211-1212 A germacranolide from Cyathocline lutea S.R. Rojatkar, M. Banerjee, D.D. Sawaikar, B.A. Nagasampagi Structure 13C NMR ̼Æ×Ä£Äâͼ 33 . 5,5,9-Èý¼×»ù-1-ôǼ׻ùÂÝ[5.5]-8-ʮһϩ-3-ͪ(b) ÏàËÆ¶È:53.3% Chemical Journal of Chinese Universities 2003 24 1820-1824 Total Synthesis of (¡À)-¦Á-Chamigrene-3-one WANG Jin-Jun, YIN Jun-Gang, WU Xu-Ran, ZHAO Yan,TAKESHITA Histoshi, MORIA kira, HATSUI Toshihide Structure 13C NMR ̼Æ×Ä£Äâͼ 34 . compound 49 C14H20O ÏàËÆ¶È:53.3% Canadian Journal of Chemistry 2006 84 1456-1469 Intramolecular [4 + 3] cycloadditions -Stereochemical issues in the cycloaddition reactions of cyclopentenyl cations - A synthesis of (+)-dactylol1 Michael Harmata, Paitoon Rashatasakhon, and Charles L. Barnes Structure 13C NMR ̼Æ×Ä£Äâͼ 35 . hydroxyenone ÏàËÆ¶È:53.3% Organic Letters 2003 Vol. 5, No. 13 2295-2298 Enantiospecific First Total Synthesis and Assignment of Absolute Configuration of the Sesquiterpene (-)-Cucumin H A. Srikrishna and Dattatraya H. Dethe Structure 13C NMR ̼Æ×Ä£Äâͼ 36 . 1-Methyl-2-{[(1R,2R,5R)-6,6-dimethylbicyclo[3.1.1]heptyl-2]methylsulfonyl}-1H-imidazole C14H22N2O2S ÏàËÆ¶È:53.3% Chemistry of Natural Compounds 2012 48 38-42 SYNTHESIS OF NEW MONOTERPENE SULFONYLIMIDAZOLES M. Ya. Demakova,D. V. Sudarikov,S. A. Rubtsova,L. L. Frolova,and A. V. Kuchin Structure 13C NMR ̼Æ×Ä£Äâͼ 37 . 3-keto-drimenol C15H24O2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2009 57 433-435 Sesquiterpenes from Cultures of the Basidiomycete Clitocybe conglobata and Their 11¦Â-Hydroxysteroid Dehydrogenase Inhibitory Activity Di Xu, Yu Sheng, Zhong-Yu Zhou, Rong Liu, Ying Leng and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 38 . 3-keto-drimenol C15H24N2 ÏàËÆ¶È:53.3% Chemical & Pharmaceutical Bulletin 2009 57 433-435 Sesquiterpenes from Cultures of the Basidiomycete Clitocybe conglobata and Their 11¦Â-Hydroxysteroid Dehydrogenase Inhibitory Activity Di Xu, Yu Sheng, Zhong-Yu Zhou, Rong Liu, Ying Leng and Ji-Kai Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 39 . neopulchellin ÏàËÆ¶È:53.3% Phytochemistry 1988 27 2887-2891 Sesquiterpene lactones from Gaillardia pulchella Sanggong Yu,Nianbai Fang,Tom J. Mabry,Khalil A. Abboud,Stanley H. Simonsen Structure 13C NMR ̼Æ×Ä£Äâͼ 40 . compound 7 ÏàËÆ¶È:53.3% Phytochemistry 1990 29 977-979 Oplopanes from the leaves of Senecio mexicanus Pedro Joseph-Nathan,J.Roberto Villag¨®mez,Luisa U. Rom¨¢n,Juan D. Hern¨¢ndez Structure 13C NMR ̼Æ×Ä£Äâͼ 41 . 11¦Â,13-dihydrosantamarin 3,4¦Á-epoxyde C15H22O4 ÏàËÆ¶È:53.3% Phytochemistry 1990 29 2913-2917 Sesquiterpene lactones from Artemisia caerulescens Subsp. gargantae Juan F. Sanzand,J.Alberto Marco Structure 13C NMR ̼Æ×Ä£Äâͼ 42 . tannunolide C ÏàËÆ¶È:53.3% Phytochemistry 1990 29 3575-3580 Guaianolides from Tanacetum annuum Alejandro F. Barrero,Juan F. S¨¢nchez,Jos¨¦ Molina,Antonio Barr¨®n,M del Mar Salas Structure 13C NMR ̼Æ×Ä£Äâͼ 43 . Cosmosoic Acid C15H22O3 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2010 93 753-756 Two Novel 15(10¡ú1)Abeomuurolane Sesquiterpenes from Cosmos sulphureus Jyh-Horng Wu, Yi-Fu Chang, Yu-Tang Tung, Minoru Tsuzuki, Akira Izuka, Sheng-Yang Wang and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 44 . Cosmosaldehyde C15H22O2 ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2010 93 753-756 Two Novel 15(10¡ú1)Abeomuurolane Sesquiterpenes from Cosmos sulphureus Jyh-Horng Wu, Yi-Fu Chang, Yu-Tang Tung, Minoru Tsuzuki, Akira Izuka, Sheng-Yang Wang and Yueh-Hsiung Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 45 . 2¦Â-hydroxy-( + )-prezizane ÏàËÆ¶È:53.3% Phytochemistry 1981 20 1597-1599 Jinkohol, a prezizane sesquiterpene alcohol from agarwood Tsutomu Nakanishi, Etsuko Yamagata, Kaisuke Yoneda, Iwao Miura Structure 13C NMR ̼Æ×Ä£Äâͼ 46 . eremoligularin C15H22O4 ÏàËÆ¶È:53.3% Tetrahedron Letters 2004 45 8855-8858 Bieremoligularolide and eremoligularin, two novel sesquiterpenoids from Ligularia muliensis Qiu-Hong Wu, Chun-Ming Wang, Sheng-Gao Cheng, Kun Gao Structure 13C NMR ̼Æ×Ä£Äâͼ 47 . (1R,6R,7R,10S)-6-Hydroxy-7-(1-methylethyl)-10-methylbicyclo[4.4.0]decan-4-one C14H24O2 ÏàËÆ¶È:53.3% Journal of the Chemical Society, Perkin Transactions 1 2000 189-194 Synthesis of sesquiterpene allylic alcohols and sesquiterpene dienes from Cupressus bakeri and Chamaecyparis obtusa Koon-Sin Ngo and Geoffrey D. Brown Structure 13C NMR ̼Æ×Ä£Äâͼ 48 . jinkohol ÏàËÆ¶È:53.3% Journal of the Chemical Society, Perkin Transactions 1 1983 601-604 Jinkoh-eremol and jinkohol II, two new sesquiterpene alcohols from agarwood Tsutomu Nakanishi, Etsuko Yamagata, Kaisuke Yoneda, Iwao Miura and Hideo Mori Structure 13C NMR ̼Æ×Ä£Äâͼ 49 . 10¦ÂH,11¦ÁH-7¦Á-Hydroxy-8-oxoeremophilan-12,6-olide C15H22O4 ÏàËÆ¶È:53.3% Tetrahedron 2008 64 9136-9142 Isolation of new eremophilane-type sesquiterpenoids, subspicatins A¨CD and subspicatolide from Ligularia subspicata, and chemical and genetic diversity of the species Motoo Tori, Yasuko Okamoto, Kana Tachikawa, Kanako Mihara, Aki Watanabe, Misato Sakaoku, Shigeru Takaoka, Masami Tanaka, Xun Gong, Chiaki Kuroda, Masato Hattori, Ryo Hanai Structure 13C NMR ̼Æ×Ä£Äâͼ 50 . compound 25 C15H20O5I ÏàËÆ¶È:53.3% The Journal of Organic Chemistry 2002 67 5461-5469 Synthesis of (+)-8-Deoxyvernolepin and Its 11,13-Dihydroderivative. A Novel Reaction Initiated by Sulfene Elimination Leads to the 2-Oxa-cis-decalin Skeleton Alejandro F. Barrero, J. Enrique Oltra, M¨ªriam ¨¢lvarez, and Antonio Rosales Structure 13C NMR ̼Æ×Ä£Äâͼ 51 . (1R,7S,8S)-7-hydroxy-1,4,4,8-tetramethyltricyclo[6.3.0.02,6]undec-2(6)-en-3-one, C15H22O2 ÏàËÆ¶È:53.3% Indian Journal of Chemistry Section B 2011 50B 1092-1106 Enantiospecific first total synthesis of cucumin-H Srikrishna, A; Dethe, Dattatraya H Structure 13C NMR ̼Æ×Ä£Äâͼ 52 . (2aR,4aR,5R,7aR,7bS)-5-hydroxy-2,2,4a-tri-methyldecahydrocyclobuta[e]indene-7a-carbaldehyde C15H24O2 ÏàËÆ¶È:53.3% Russian Journal of Organic Chemistry 2004 40 1441-1449 Transformations of caryophyllene diepoxides in various acidic media O. V. Salomatina, D. V. Korchagina, Yu. V. Gatilov, M. P. Polovinka and V. A. Barkhash Structure 13C NMR ̼Æ×Ä£Äâͼ 53 . agripilolactone C15H24O3 ÏàËÆ¶È:53.3% Journal of Chemical Research 2011 35 116-118 A new sesquiterpenoid from a Fusarium spp. an endophytic fungus in Agriminia pilosa Wang, Jian-Wei; Li, Cheng-Ping Structure 13C NMR ̼Æ×Ä£Äâͼ 54 . (3aS,5aR,6R,7R,8R,9S,9aS,9bS)-6,7,8,9-diepoxy-5a,9-dimethyl-3-methylidene-5. 3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-2-one C15H18O4 ÏàËÆ¶È:53.3% Phytochemistry 2012 80 70-76 Sesquiterpenes from the leaves of Laurus nobilis L. Elin Julianti, Kyoung Hwa Jang, Sooryun Lee, Dongha Lee, Woongchon Mar, Ki-Bong Oh, Jongheon Shin Structure 13C NMR ̼Æ×Ä£Äâͼ 55 . (-)-(3R)-3-hydroxy-isolongifolol C15H26O2 ÏàËÆ¶È:53.3% Journal of Oleo Science 2010 59 243-246 Microbial Transformation of (-)-Isolongifolol by Plant Pathogenic Fungus Glomerella cingulata Mitsuo Miyazawa, Kazuki Sakata, Masashi Ueda Structure 13C NMR ̼Æ×Ä£Äâͼ 56 . ¦Â-cyclocostunolide ÏàËÆ¶È:53.3% Phytochemistry 2013 95 19-93 Sesquiterpenoids in subtribe Centaureinae (Cass.) Dumort (tribe Cardueae, Asteraceae): Distribution, 13C NMR spectral data and biological properties Review Article Maurizio Bruno, Svetlana Bancheva, Sergio Rosselli, Antonella Maggio Structure 13C NMR ̼Æ×Ä£Äâͼ 57 . gomerolactone D C15H21ClO3 ÏàËÆ¶È:53.3% European Journal of Organic Chemistry 2009 2009 1407-1411 Novel Lactone Chamigrene-Derived Metabolites from Laurencia majuscula Ana R. D¨ªaz-Marrero, Inmaculada Brito, Jos¨¦ M. de la Rosa, Luis D'Croz, Oscar Fabelo, Catalina Ruiz-P¨¦rez, Jos¨¦ Darias and Mercedes Cueto Structure 13C NMR ̼Æ×Ä£Äâͼ 58 . 1,7-dimethyltricyclo[6.2.2.0(4,9)]dodec-6-en-3-one C14H20O 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 59 . jinkohol ÏàËÆ¶È:53.3% Flavour and Fragrance Journal 2000 15 61-83 1,7-Cyclogermacra-1(10),4-dien-15-al, a sesquiterpene with a novel skeleton, and other sesquiterpenes from Haitian vetiver oil Peter Weyerstahl, Helga Marschall, Ute Splittgerber and Dietmar Wolf Structure 13C NMR ̼Æ×Ä£Äâͼ 60 . (-)-10-oxo-isodauc-3-en-15-oic acid C15H22O3 ÏàËÆ¶È:53.3% Journal of Natural Medicines 2012 66 453-458 Pyrenes and pyrendiones from Uvaria lucida Masataka Moriyasu, Sousuke Takeuchi, Momoyo Ichimaru, Noriyshi Nakatani and Yumi Nishiyama, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 61 . eremoligularin ÏàËÆ¶È:53.3% Chinese Traditional and Herbal Drugs 2012 43 1270-1272 Chemical constituents of Ligularia intermedia from Henan Province YUAN Yong-liang; YE Dan-dan; LIANG Hui-juan; LIU Wei; BAI Su-ping Structure 13C NMR ̼Æ×Ä£Äâͼ 62 . ¦Â-cyclocostunolide ÏàËÆ¶È:53.3% China Journal of Chinese Materia Medica 2012 37 1232-1236 Chemical constituents from a portion of ethanolicextract of Saussurea lappa roots ZHANG Ting; MA Lin; WU Feng; CHEN Ruoyun Structure 13C NMR ̼Æ×Ä£Äâͼ 63 . ¦Â-cyclocostunolide ÏàËÆ¶È:53.3% China Journal of Chinese Materia Medica 2012 37 1249-1253 Chemical constituents of Dolomiaea souliei WEI Hua; HE Chunnian; PENG Yong; MA Guoxu; XIAO Peigen Structure 13C NMR ̼Æ×Ä£Äâͼ 64 . kobusone ÏàËÆ¶È:53.3% China Journal of Chinese Materia Medica 2012 37 1973-1976 Sesquiterpenes and monoterpene from Aquilaria sinensis YANG Lin; QIAO Lirui; XIE Dan; DAI Jungui; GUO Shunxing Structure 13C NMR ̼Æ×Ä£Äâͼ 65 . compound 4a C17H21NO2 ÏàËÆ¶È:53.3% Chinese Journal of Organic Chemistry 2013 33 2196-2204 Synthesis and Antibacterial Activity of New Pinanyl Nitrogen-Containing Heterocycles Wei Baisong, Gu Wen, Xu Xu, Yang Yiqin, Wang Shifa Structure 13C NMR ̼Æ×Ä£Äâͼ 66 . compound 4b C17H20NO2Cl ÏàËÆ¶È:53.3% Chinese Journal of Organic Chemistry 2013 33 2196-2204 Synthesis and Antibacterial Activity of New Pinanyl Nitrogen-Containing Heterocycles Wei Baisong, Gu Wen, Xu Xu, Yang Yiqin, Wang Shifa Structure 13C NMR ̼Æ×Ä£Äâͼ 67 . compound 25 ÏàËÆ¶È:53.3% Magnetic Resonance in Chemistry 1987 25 619-627 Structural studies in the cedrane series by 13C NMR P. Brun, J. Casanova, Muppala S. Raju, B. Waegell, Ernest Wenkert and J. P. Zahra Structure 13C NMR ̼Æ×Ä£Äâͼ 68 . compound 26 ÏàËÆ¶È:53.3% Magnetic Resonance in Chemistry 1987 25 619-627 Structural studies in the cedrane series by 13C NMR P. Brun, J. Casanova, Muppala S. Raju, B. Waegell, Ernest Wenkert and J. P. Zahra Structure 13C NMR ̼Æ×Ä£Äâͼ 69 . lycopodatine A C17H28NO2 ÏàËÆ¶È:52.9% Journal of Natural Products 2005 68 1809-1812 Lycopodatines A−C, C16N Alkaloids from Lycopodium inundatum Hiroshi Morita, Yusuke Hirasawa, and Jun'ichi Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 70 . 11¦Á,13-dihgdrochamissonolide ÏàËÆ¶È:52.9% Planta Medica 1995 61 544-550 Sesquiterpene Lactones and Inositol Esters from Arnica angustfolial Thomas J. Schmidt, G¨¹nter Willuhn. Alois Steigel, andDetlefWendisch Structure 13C NMR ̼Æ×Ä£Äâͼ 71 . 11¦Á,13-dihydro-6-deoxychamissonolide ÏàËÆ¶È:52.9% Planta Medica 1995 61 544-550 Sesquiterpene Lactones and Inositol Esters from Arnica angustfolial Thomas J. Schmidt, G¨¹nter Willuhn. Alois Steigel, andDetlefWendisch Structure 13C NMR ̼Æ×Ä£Äâͼ 72 . turberostemoninol C22H29NO6 ÏàËÆ¶È:52.9% Chinese Chemical Letters 1993 4 1067-1070 TWO MINOR ALKLOIDS FROM THE ROOTS OF STEMONA TUBEROSA WEN HAN LIN,LEI WANG LIANG QIAO,MENG SHEN CAI Structure 13C NMR ̼Æ×Ä£Äâͼ 73 . 10-epi-Dihydrobotrydial C17H28O5 ÏàËÆ¶È:52.9% Phytochemistry 1996 41 513-517 Biologically active sesquiterpenoid metabolites from the fungus Botrytis cinerea Isidro G. Collado, Rosario Hern¨¢ndez-Gal¨¢n, Victoria Prieto, James R. Hanson, Laureana G. Rebordinos Structure 13C NMR ̼Æ×Ä£Äâͼ 74 . stcmominoamide C17H23NO4 ÏàËÆ¶È:52.9% Phytochemistry 1994 36 1333-1335 Two minor alkaloids from roots of Stemona tuberosa Wen Han Lin, Li Ma, Meng Shen Cai, Roderick A. Barnes Structure 13C NMR ̼Æ×Ä£Äâͼ 75 . 4-O-acetyl-11¦ÁH,13-dihydrorudmollin C17H26O5 ÏàËÆ¶È:52.9% Phytochemistry 1992 31 2051-2054 Sesquiterpene lactones and other constituents from Rudbeckia mollis Marta Vasquez, Leovigildo Quijano, Lowell E. Urbatsch, Nikolaus H. Fischer Structure 13C NMR ̼Æ×Ä£Äâͼ 76 . lycopodatines A C17H27NO2 ÏàËÆ¶È:52.9% Heterocycles 2009 77 679-729 The Lycopodium Alkaloids Yusuke Hirasawa, Jun'ichi Kobayashi, and Hiroshi Morita Structure 13C NMR ̼Æ×Ä£Äâͼ 77 . 2¦Á-Acetoxy-11¦Á,l3-dihydroconfertin C15H22O4 ÏàËÆ¶È:52.9% Phytochemistry 1985 24 1017-1019 Pseudoguaianolides related to confertin from Stevia isomeca Ferdinand Bohlmann, Kazuyasu Umemoto, Jasmin Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ 78 . lycoflexine ÏàËÆ¶È:52.9% Tetrahedron Letters 2002 43 8307-8311 Seven new Lycopodium alkaloids, lycoposerramines-C, -D, -E, -P, -Q, -S, and -U, from Lycopodium serratum Thunb. Hiromitsu Takayama, Kazuaki Katakawa, Mariko Kitajima, Kentaro Yamaguchi, Norio Aimi Structure 13C NMR ̼Æ×Ä£Äâͼ 79 . (1S,8R,9S)-9-isopropyl-8-(methoxymethoxy)-1-methylbicyclo[6.3.0]undec-5-en-3-ol C17H30O3 ÏàËÆ¶È:52.9% Indian Journal of Chemistry Section B 2011 50B 73-76 Enantiospecific approach to AB-ring system of the diterpenes fusicoccanes Srikrishna, A; Nagaraju, Gopalasetty Structure 13C NMR ̼Æ×Ä£Äâͼ 80 . compound 13 ÏàËÆ¶È:52.6% Steroids 1992 57 306-312 Studies on anabolic steroids. 9. Tertiary sulfates of anabolic 17¦Á-methyl steroids: synthesis and rearrangement Honggang Bi, Robert Mass¨¦, George Just Structure 13C NMR ̼Æ×Ä£Äâͼ 81 . oxandrolone ÏàËÆ¶È:52.6% Steroids 1992 57 537-550 17-Epimerization of 17¦Á-methyl anabolic steroids in humans: metabolism and synthesis of 17¦Á-hydroxy-17¦Â-methyl steroids Willi Schänzer, Georg Opfermann, Manfred Donike Structure 13C NMR ̼Æ×Ä£Äâͼ 82 . decarboxywedeligenin ÏàËÆ¶È:52.6% Organic Magnetic Resonance 1982 18 138-142 13C NMR spectra of wedeloside and related kaurenoid derivatives I. A. S. Lewis and J. K. MacLeod Structure 13C NMR ̼Æ×Ä£Äâͼ 83 . ( R,1- S,3¦ÁR,4S,8¦ÁS,9S)- Decahydro- ,4,8,8-tetramethyl-1,4-methanoazulene-9-methanol ÏàËÆ¶È:50% Helvetica Chimica Acta 2003 Vol. 86 106 The Ozonolysis of Longifolene: A Tool for the Preparation of Useful Chiral Compounds. Configuration Determination of New StereogenicCenters by NMR Spectroscopy and X-Ray Crystallography Vladimir Dimitrov, Gudrun Hopp Rentsch, Anthony Linden, and Manfred Hesse Structure 13C NMR ̼Æ×Ä£Äâͼ 84 . (S,1S,3¦ÁR,4S,8¦ÁS,9S)-Decahydro- ,4,8,8-tetramethyl-1,4-methanoazulene-9-methanol ÏàËÆ¶È:50% Helvetica Chimica Acta 2003 Vol. 86 106 The Ozonolysis of Longifolene: A Tool for the Preparation of Useful Chiral Compounds. Configuration Determination of New StereogenicCenters by NMR Spectroscopy and X-Ray Crystallography Vladimir Dimitrov, Gudrun Hopp Rentsch, Anthony Linden, and Manfred Hesse Structure 13C NMR ̼Æ×Ä£Äâͼ 85 . 1¦Á,3¦Â-dihydroxyambrox C16H28O3 ÏàËÆ¶È:50% Journal of Natural Products 2006 69(6) 957-959 Biotransformation of (− -Ambrox by Cell Suspension Cultures of Actinidia deliciosaAsma Nasib, Syed Ghulam Musharraf, Sajjad Hussain, Saifullah Khan,Shazia Anjum, Shamsher Ali, Atta-ur-Rahman, and M. Iqbal Choudhary Structure 13C NMR ̼Æ×Ä£Äâͼ 86 . compound 2a C18H34O4 ÏàËÆ¶È:50% Journal of Natural Products 2007 70 575-583 Megastigmanes and Their Glucosides from the Whole Plant of Sedum sarmentosum Masayuki Yoshikawa,Toshio Morikawa, Yi Zhang,Seikou Nakamura, Osamu Muraoka, and Hisashi Matsuda Structure 13C NMR ̼Æ×Ä£Äâͼ 87 . serratine C16H25NO3 ÏàËÆ¶È:50% Journal of Natural Products 2007 70 1024-1028 Fawcettimine-Related Alkaloids from Lycopodium serratum Kazuaki Katakawa,Akiko Nozoe,Noriyuki Kogure, Mariko Kitajima,Masakiyo Hosokawa, and Hiromitsu Takayama Structure 13C NMR ̼Æ×Ä£Äâͼ 88 . 4¦Á-acetyl-guaia-1(10)-en-13¦Á-methyl-12,8¦Â-olide C17H24O4 ÏàËÆ¶È:50% Journal of Natural Products 1999 62 920-922 Oxidative Transformations of Guaia-1(10)-en-12, 8-olides into Xanthanolides Mariano Mart¨ªnez-V¨¢zquez, Jorge C¨¢rdenas, Lucas Godoy, Martha Mart¨ªnez-Bahena, Ren¨¦ Miranda, and Manuel Salm¨®n Structure 13C NMR ̼Æ×Ä£Äâͼ 89 . 2¦Â-hydroxy-8,15(R)-oxydo-ent-pimaran C20H34O3 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1983 31 4409-4416 Chemische und Chemotaxonomische Untersuchungen der Pterophyten. XLIV. Chemische Untersuchungen der Inhaltsstoffe von Microlepia marginata (PANZER) C. CHR. (2) TADAYUKI KURAISHI,TAKAO TANIGUCHI,KAZUYUKI HORI,TAKAO MURAKAMI,NOBUTOSHI TANAKA,YASUHISA SAIKI and CHIUMING CHEN Structure 13C NMR ̼Æ×Ä£Äâͼ 90 . abbeokutone ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2008 33 1566-1568 Studies on chemical constituents from stem bark of Trwia nudiflora WU Shaohua, SHENG Yuemao, CHEN Youwei, YANG Liyuan, LI Shaolan, LI Zhiying Structure 13C NMR ̼Æ×Ä£Äâͼ 91 . ¦Á-hydroxy-10¦Á-methoxyguaian-12,6-olide C16H26O4 ÏàËÆ¶È:50% Phytochemistry 1998 49 559-564 Antimycobacterial evaluation of germacranolides in honour of professor G.H. Neil Towers 75th birthday Nikolaus H. Fischer, Tiansheng Lu, Charles L. Cantrell, Jos¨¦ Castañeda-Acost¦Á, Leovigildo Quijano, Scott G. Franzblau Structure 13C NMR ̼Æ×Ä£Äâͼ 92 . compound 13 ÏàËÆ¶È:50% Journal of Natural Products 1984 Vol 47 592-599 Cmr Spectroscopy of Labdanic Diterpenes and Related Substances Josette Bastard, Do Khac Duc, Marcel Fetizon, Malcolm J. Francis, Peter K. Grant, Rex T. Weavers, Chikara Kaneko, G. Vernon Baddeley, Jean-Marie Bernassau, Ivor R. Burfitt, Peter M. Wovkulich, Ernest Wenkert Structure 13C NMR ̼Æ×Ä£Äâͼ 93 . methyl 4-(2-hydroxy-1,5-dimethyl-3-oxohexyl)-1-cyclo-hexene-1-carboxylate C16H26O4 ÏàËÆ¶È:50% Phytochemistry 1993 32 1163-1165 Juvabione analogues from two Abies sachalinensis trees Kenzo Kawai, Chika Takahashi, Tamie Takada, Atsushi Numata Structure 13C NMR ̼Æ×Ä£Äâͼ 94 . 4¦Â,10¦Â-dihydroxy-1¦Á-methoxy-5¦Á,11¦ÁH-guaia-2-en-12,6¦Á-olide C16H24O5 ÏàËÆ¶È:50% 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 95 . compound 4 ÏàËÆ¶È:50% Phytochemistry 1991 30 4177-4179 A triterpenoid glucoside from Barringtonia acutangula Bikas C. Pal, Basudeb Achari, Keith R. Price Structure 13C NMR ̼Æ×Ä£Äâͼ 96 . methyl 4-[2,3,3-trimethyl-6,9-dithiaspiro[4.4]-non-2-yl]-4-pentenoate C16H26O2S2 ÏàËÆ¶È:50% Indian Journal of Chemistry Section B 2007 46B 805-817 Total synthesis of (¡À)-¦Â-microbiotene,(¡À)-microbiotol,(¡À)-cyclocuparanol and (¡À)-¦Â-cuparenones Srikrishna,A; Ramachary,D B Structure 13C NMR ̼Æ×Ä£Äâͼ 97 . Longibornyl acetate ÏàËÆ¶È:50% Phytochemistry 1985 24 2893-2898 Foliage sesquiterpenes of Dacrydium cupressinum: identification, variation and biosynthesis Katherine M. Berry, Nigel B. Perry, Rex T. Weavers Structure 13C NMR ̼Æ×Ä£Äâͼ 98 . compound Ia ÏàËÆ¶È:50% Steroids 1983 41 493-500 Metabolism of 17¦Á-methyl-5¦Â-dihydrotestosterone in the rabbit John F. Templeton, Chung-Ja Choi Jackson Structure 13C NMR ̼Æ×Ä£Äâͼ 99 . compound VIIa ÏàËÆ¶È:50% Steroids 1983 41 493-500 Metabolism of 17¦Á-methyl-5¦Â-dihydrotestosterone in the rabbit John F. Templeton, Chung-Ja Choi Jackson Structure 13C NMR ̼Æ×Ä£Äâͼ 100 . compound 14 ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 5617-5620 Free radical reactions for heterocycle synthesis. Part 5: Formation of novel bridged spirolactones by double cyclizations Wei Zhang, Georgia Pugh Structure 13C NMR ̼Æ×Ä£Äâͼ 101 . compound 24a C16H24O4 ÏàËÆ¶È:50% Tetrahedron Letters 2004 45 383-386 Carbanion cyclisation of esters. Part 2: Enantiospecific construction of the tricyclic framework of the marine sesquiterpenes, spirodysins A. Srikrishna, P. Ravi Kumar, S.S.V. Ramasastry Structure 13C NMR ̼Æ×Ä£Äâͼ 102 . Isopimara-7,15-dien-1¦Â,19-diol C20H32O2 ÏàËÆ¶È:50% Tetrahedron 2012 68 819-829 Potential anti-inflammatory diterpenes from Premna obtusifolia Abdul-Wahab Salae, Apinya Rodjun, Chatchanok Karalai, Chanita Ponglimanont, Suchada Chantrapromma, Akkharawit Kanjana-Opas, Supinya Tewtrakul, Hoong-Kun Fun Structure 13C NMR ̼Æ×Ä£Äâͼ 103 . (R)-ethyl-5-((1R,3aR,7aR)-7a-methyl-4-oxo-octahydro-1H-inden-1-yl)hexanoate ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2010 18 4119-4137 Vitamin D receptor agonist/histone deacetylase inhibitor molecular hybrids Marc Lamblin, Basel Dabbas, Russell Spingarn, Rodrigo Mendoza-Sanchez, Tian-Tian Wang, Beum-Soo An, Dao Chao Huang, Richard Kremer, John H. White, James L. Gleason Structure 13C NMR ̼Æ×Ä£Äâͼ 104 . Cermizine D C16H30N2 ÏàËÆ¶È:50% Tetrahedron 2004 60 7015-7023 New phlegmarane-type, cernuane-type, and quinolizidine alkaloids from two species of Lycopodium Hiroshi Morita, Yusuke Hirasawa, Takakazu Shinzato, Jun'ichi Kobayashi Structure 13C NMR ̼Æ×Ä£Äâͼ 105 . 3¦Á,17-dihydroxyspongia-13(16),14-dien-2-one C20H28O4 ÏàËÆ¶È:50% Tetrahedron 1994 50 9893-9908 Scalemic 12-hydroxyambliofuran and 12-acetoxy-ambliofuran, five tetracyclic furanoditerpenes and a furanosesterterpene from Spongia sp. Philip A. Searle, Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ 106 . (1S,5R,8S,10S,11R)-10-(methoxymethoxy)-8,10,11-trimethyltricyclo[6.3.0.01,5]undecan-4-one C16H26O3 ÏàËÆ¶È:50% Tetrahedron 2012 68 2650-2656 Enantiospecific first total synthesis of (6S,7R)-silphiperfolan-6-ol A. Srikrishna, Gopalasetty Nagaraju, Vishal M. Sheth Structure 13C NMR ̼Æ×Ä£Äâͼ 107 . O-methyldihydrobotrydial C18H30O5 ÏàËÆ¶È:50% Agricultural and Biological Chemistry 1988 52 1845-1847 Isolation and Structures of O-Methyldihydrobotrydial and Deacetyl-O-methyldihydrobotrydialone Produced by Botrytis squamosa Yasuo KIMURA, Hiroaki FUJIOKA, Hiromitsu NAKAJIMA, Takashi HAMASAKI, Akira ISOGAI Structure 13C NMR ̼Æ×Ä£Äâͼ 108 . (1S*,2S*,3R*,6R*,7S*,9R*)-(-)-2-thiocyanatoneopupukeanane C16H25NS ÏàËÆ¶È:50% Australian Journal of Chemistry 1997 50 1123-1127 Terpene Metabolites from the Tropical Marine Sponge Axinyssa sp. nov. Jamie S. Simpson,, Mary J. Garson,, John N. A. Hooper,, Edith I. Cline and Cindy K. Angerhofer Structure 13C NMR ̼Æ×Ä£Äâͼ 109 . (8a¦Â,12a¦Â,13a¦Á)-5,8,8a,9,10,11,12,12a,13,13a-decahydro-8-oxo-6H-isoquino[2,1-g][1,6]naphthyridine C16H20N2O ÏàËÆ¶È:50% Journal of Medicinal Chemistry 1991 34 705-717 Structure-affinity relationships of 12-sulfonyl derivatives of 5,8,8a,9,10,11,12,12a,13,13a-decahydro-6H-isoquino[2,1-g][1,6]naphthyridines at .alpha.-adrenoceptors Robin D. Clark, David B. Repke, Jacob Berger, Janis T. Nelson, Andrew T. Kilpatrick, Christine M. Brown, Alison C. MacKinnon, Ruth U. Clague, Michael Spedding Structure 13C NMR ̼Æ×Ä£Äâͼ 110 . compound 12 C16H24O3 ÏàËÆ¶È:50% Tetrahedron 2013 69 1363-1368 From toluene to triquinanes: formal total syntheses of the sesquiterpenoid natural products (− -hypnophilin and (− -coriolinDavid J.-Y.D. Bon, Martin G. Banwell, Jas S. Ward, Anthony C. Willis Structure 13C NMR ̼Æ×Ä£Äâͼ 111 . compound 8 C18H32O4 ÏàËÆ¶È:50% European Journal of Organic Chemistry 2005 2005 5077-5083 Antimalarial Polyketide Cycloperoxides from the Marine SpongePlakortis simplex Claudio Campagnuolo, Ernesto Fattorusso, Adriana Romano, Orazio Taglialatela-Scafati, Nicoletta Basilico, Silvia Parapini and Donatella Taramelli Structure 13C NMR ̼Æ×Ä£Äâͼ 112 . compound 35 ÏàËÆ¶È:50% Canadian Journal of Chemistry 1979 57 1550-1556 13C nuclear magnetic resonance studies. 85. 13C spectra of several ring-contracted and -expanded steroids Vinod Dave, J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 113 . compound 38 ÏàËÆ¶È:50% Canadian Journal of Chemistry 1979 57 1550-1556 13C nuclear magnetic resonance studies. 85. 13C spectra of several ring-contracted and -expanded steroids Vinod Dave, J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 114 . compound 48 ÏàËÆ¶È:50% Canadian Journal of Chemistry 1979 57 1550-1556 13C nuclear magnetic resonance studies. 85. 13C spectra of several ring-contracted and -expanded steroids Vinod Dave, J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 115 . compound 49a ÏàËÆ¶È:50% Canadian Journal of Chemistry 1979 57 1550-1556 13C nuclear magnetic resonance studies. 85. 13C spectra of several ring-contracted and -expanded steroids Vinod Dave, J. B. Stothers Structure 13C NMR ̼Æ×Ä£Äâͼ 116 . compound 10b ÏàËÆ¶È:50% Chemistry-A European Journal 2006 12 6572-6584 Asymmetric Total Syntheses of Marine Cyclic Depsipeptide Halipeptins A¨CD Shouyun Yu, Xianhua Pan and Dawei Ma Structure 13C NMR ̼Æ×Ä£Äâͼ 117 . (+)-2-[(1S,2R,4aS,8aS)-decahydro-2,5,5,8a-tetramethylnaphthalen-1-yl]oxirane ÏàËÆ¶È:50% Helvetica Chimica Acta 2014 97 197-214 Enantioselective Access to (− -Ambrox® Starting from ¦Â-FarneseneChristian Chapuis Structure 13C NMR ̼Æ×Ä£Äâͼ 118 . compound 6-Me C16H24O3 ÏàËÆ¶È:50% Journal of Natural Medicines 2012 66 453-458 Pyrenes and pyrendiones from Uvaria lucida Masataka Moriyasu, Sousuke Takeuchi, Momoyo Ichimaru, Noriyshi Nakatani and Yumi Nishiyama, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 119 . rhodomollein F C20H32O6 ÏàËÆ¶È:50% Journal of Asian Natural Products Research 2012 14 764-768 Two new grayanane diterpenoids from the flowers of Rhododendron molle Zhi-Run Zhang, Jin-Dong Zhong, Hong-Mei Li, Hai-Zhou Li, Rong-Tao Li & Xu-Liang Deng Structure 13C NMR ̼Æ×Ä£Äâͼ 120 . (16R)-16,17-Dihydroxy-ent-kaur-2-one C20H32O3 ÏàËÆ¶È:50% Chemistry of Natural Compounds 2013 48 999-1001 A new ent-kaurane diterpenoid from Rubus corchorifolius Yang-Wen Ou, Xue-Xiang Chen, Min Zhang, Xiao-Juan Liu Structure 13C NMR ̼Æ×Ä£Äâͼ |

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