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1 . N-pentanoyl-4-(aminomethyl)-6-methoxy-9-methyl-1,2,3,4-tetrahydrocarbazole C20H28N2O2 ÏàËÆ¶È:75% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 2-methoxy-5,6,7,8,10,11-hexahydro-9H-6,10-methanocyclooctaindol-9-one C16H17NO2 ÏàËÆ¶È:73.6% Russian Journal of Organic Chemistry 2007 43 1196-1201 Synthetic approach to preparation of indole derivatives fused with a bicyclo[3.3.1]nonane framework T. Yu. Baranova, O. N. Zefirova, N. V. Averina, V. V. Boyarskikh and G. S. Borisova, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . N-butanoyl-4-(aminomethyl)-6-methoxy-9-methyl-1,2,3,4-tetrahydrocarbazole C19H26N2O2 ÏàËÆ¶È:73.6% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . N-cyclopropanoyl-4-(aminomethyl)-6-methoxy-9-methyl-1,2,3,4-tetrahydrocarbazole C19H24N2O2 ÏàËÆ¶È:73.6% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . N-pentanoyl-10-(aminomethyl)-2-methoxy-5-methyl-5,6,7,8,9,10-hexahydrocycloheptindole C21H30N2O2 ÏàËÆ¶È:71.4% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (¡À)-2-allyl-1-[3-(4-methoxybenzyloxy)propyl]-2,3-dimethylcyclohexan-1-trimethylsilyloxyether ÏàËÆ¶È:71.4% Journal of the Brazilian Chemical Society 2001 12 360-367 An Approach to the Construction of the Carbon Skeleton of Marine Nor-sesquiterpenes. Total Synthesis of (¡À)-Dehalo-Napalilactone. Gaspar Diaz and Fernando Coelho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . compound 11a C22H34O3 ÏàËÆ¶È:70% Tetrahedron 2002 58 1647-1656 Studies on the synthesis of (¡À)-pathylactone A, a nor-sesquiterpene lactone isolated from marine sources Fernando Coelho, Gaspar Diaz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . N-butanoyl-10-(aminomethyl)-2-methoxy-5-methyl-5,6,7,8,9,10-hexahydrocycloheptindole C20H28N2O2 ÏàËÆ¶È:70% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (+)-2-allyl-1-[3-(4-methoxybenzyloxy)propyl]-2,3-dimethylcyclohexan-1-ol C22H34O3 ÏàËÆ¶È:70% Journal of the Brazilian Chemical Society 2001 12 360-367 An Approach to the Construction of the Carbon Skeleton of Marine Nor-sesquiterpenes. Total Synthesis of (¡À)-Dehalo-Napalilactone. Gaspar Diaz and Fernando Coelho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . compound 6 C20H26N2O2 ÏàËÆ¶È:68.4% Helvetica Chimica Acta 1999 Vol. 82 170 A New Rearrangement in Iboga Alkaloids Alberto Madinaveitia, Gabriel de la Fuente, and Antonio Gonz¨¢lez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 1,6-Anhydro-2-aminooctyl-2,3,4-trideoxy-¦Â-D-erythro-hex-3-enopyranose ÏàËÆ¶È:68.4% Chemistry of Natural Compounds 2004 40 521-525 SYNTHESIS OF 2-AMINO DERIVATIVES OF LEVOGLUCOSENONE F. A. Valeev, L. Kh. Kalimullina, Sh. M. Salikhov,O. V. Shitikova, I. P. Tsypysheva, and M. G. Safarov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 3-Hydroxy-16¦Á-methylpregn-1,3,5(10)-trien-20-one ÏàËÆ¶È:68.4% Steroids 2010 75 859-869 Stereoselective synthesis of some methyl-substituted steroid hormones and their in vitro cytotoxic activity against human gastric cancer cell line MGC-803 Chun Li, Wenwei Qiu, Zhengfeng Yang, Jian Luo, Fan Yang, Mingyao Liu, Juan Xie, Jie Tang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 3-hydroxy-5-methoxy-2-(3-hydroxy-3-methylbutyl) bibenzyl C20H26O3 ÏàËÆ¶È:68.4% Phytochemistry 1991 30 219-234 Prenyl bibenzyls from the liverwort Radula kojana Yoshinori Asakawa, Keiko Kondo, N¨¦e K. Takikawa, Motoo Tori, Toshihiro Hashimoto, Shunichi Ogawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (1r,4r)-N-(2-Hydroxyethyl)-N,N-dimethyl-4-(4-octylphenyl)cyclohexanaminium iodide C24H41NO ÏàËÆ¶È:68.4% Bioorganic & Medicinal Chemistry 2012 20 183-194 Design, synthesis and biological activity of sphingosine kinase 2 selective inhibitors Mithun R. Raje, Kenneth Knott, Yugesh Kharel, Philippe Bissel, Kevin R. Lynch, Webster L. Santos Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . (2R,3R,5S)-2-hexyl-5-[(4-methoxyphenyl)methoxy]tetrahydrofuran-3-ol C18H28O4 ÏàËÆ¶È:68.4% Heterocycles 2004 62 713-734 Stereoselective Total Synthesis of the Nonenolide (+)-Microcarpalide Martin G. Banwell* and David T. J. Loong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . (2R,3R,5R)-2-hexyl-5-[(4-methoxyphenyl)methoxy]tetrahydrofuran-3-ol C18H28O4 ÏàËÆ¶È:68.4% Heterocycles 2004 62 713-734 Stereoselective Total Synthesis of the Nonenolide (+)-Microcarpalide Martin G. Banwell* and David T. J. Loong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 7c ÏàËÆ¶È:68.4% Phytochemistry 1982 21 1725-1731 New 5-methylcoumarins from Ethulia conyzoides Vishnu S. Shukla, Subhash C. Dutta, Robindra N. Baruah, Ram P. Sharma, Gopalakrishna Thyagarajan, Werner Herz, Narendra Kumar, Kinzo Watanabe, John F. Blount Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 3,16¦Á-dihydroxyestra-1,3,5(10)-trien-17-one ÏàËÆ¶È:68.4% Steroids 1990 55 390-394 Microbiologic oxidation of estratrienes and estratetraenes by Streptomyces roseochromogenes ATCC 13400 Joan C. Ferrer, Virginia Calzada, Juan J. Bonet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . compound hc C29H46N4O5F6 ÏàËÆ¶È:68.4% Heterocycles 2000 53 1317-1328 Solution Parallel Synthesis of Cyclic Guanidines Christelle Marmillon, Jacques Bompart, Mich¨¨le Calas, Roger Escale,* and Pierre-Antoine Bonnet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 6,9-dihydro-10¦Á-hydroxyradicicol C18H21ClO6 ÏàËÆ¶È:68.4% Bioorganic & Medicinal Chemistry 2009 17 4622-4635 Synthesis and structure¨Cactivity relationships of radicicol derivatives and WNT-5A expression inhibitory activity Hideki Shinonaga, Toshiya Noguchi, Akiko Ikeda, Mari Aoki, Natsuko Fujimoto, Akira Kawashima Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . endo-N-(2-methoxy-6,7,8,9,10,11-hexahydro-5H-6,10-methanocycloocta-indol-9-yl)acetamide ÏàËÆ¶È:68.4% Russian Journal of Organic Chemistry 2007 43 1196-1201 Synthetic approach to preparation of indole derivatives fused with a bicyclo[3.3.1]nonane framework T. Yu. Baranova, O. N. Zefirova, N. V. Averina, V. V. Boyarskikh and G. S. Borisova, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 2'-methoxy-5',6',7',8',10',11'-hexahydrospiro-(1,3-dioxolane-2,9'-[6,10]methanocycloocta-indole) C18H21NO3 ÏàËÆ¶È:68.4% Russian Journal of Organic Chemistry 2007 43 1196-1201 Synthetic approach to preparation of indole derivatives fused with a bicyclo[3.3.1]nonane framework T. Yu. Baranova, O. N. Zefirova, N. V. Averina, V. V. Boyarskikh and G. S. Borisova, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . N-butanoyl-3-amino-6-methoxy-1,2,3,4-tetrahydrocarbazole C17H22N2O2 ÏàËÆ¶È:68.4% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . N-propanoyl-4-(aminomethyl)-6-methoxy-9-methyl-1,2,3,4-tetrahydrocarbazole C18H24N2O2 ÏàËÆ¶È:68.4% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . N-cyclobutanoyl-4-(aminomethyl)-6-methoxy-9-methyl-1,2,3,4-tetrahydrocarbazole C20H26N2O2 ÏàËÆ¶È:68.4% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . N-(trifluoroacetyl)-4-(aminomethyl)-6-methoxy-9-methyl-1,2,3,4-tetrahydrocarbazole C17H19N2O2F3 ÏàËÆ¶È:68.4% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 27 . N-propanoyl-10-(aminomethyl)-2-methoxy-5-methyl-5,6,7,8,9,10-hexahydrocycloheptindole C19H26N2O2 ÏàËÆ¶È:68.4% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 28 . N-cyclopropanoyl-10-(aminomethyl)-2-methoxy-5-methyl-5,6,7,8,9,10-hexahydrocycloheptindole C20H26N2O2 ÏàËÆ¶È:68.4% Journal of Medicinal Chemistry 1998 41 451-467 Mapping the Melatonin Receptor. 5. Melatonin Agonists and Antagonists Derived from Tetrahydrocyclopentindoles, Tetrahydrocarbazoles and Hexahydrocycloheptindoles David J. Davies, Peter J. Garratt, Derek A. Tocher, and Stefan Vonhoff, John Davies, Muy-Teck Teh and David Sugden Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 29 . compound 13b ÏàËÆ¶È:68.4% Journal of Medicinal Chemistry 1992 35 2459-2467 Extraordinarily potent antimalarial compounds: new, structurally simple, easily synthesized, tricyclic 1,2,4-trioxanes. Gary H. Posner, Chang Ho Oh, Lucia Gerena, Wilbur K. Milhous Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 30 . 5-amino-5-{2-[4-((1r,4r)-4-butylcyclohexyl)benzene]ethyl}-2,2-dimethyl-1,3-dioxane C24H39NO2 ÏàËÆ¶È:68.4% Archiv der Pharmazie 2012 345 93-100 Synthesis and Immunomodulating Activity of New Analogues of Fingolimod Xiang-Jun Feng, Xiao-Ying Yang, Yu Luo, Xin Li, Wei Tang, Jian-Ping Zuo and Wei Lu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 31 . (2S,3R)-2-Amino-3-benzyloxy[1,3]dioxolan-6-yl-octadecan-1-ol C27H47NO4 ÏàËÆ¶È:68.4% Heterocycles 2004 64 249-259 A Short Synthesis of (-)-Deoxoprosophylline Ang¨¦lique Jourdant and Jieping Zhu* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 32 . monacolin L ÏàËÆ¶È:68.4% Acta Pharmaceutica Sinica 2011 46 564-567 A new monacolin analogue from Xuezhikang capsule LI Xue-mei, SHEN Xing-hai, DUAN Zhen-wen, GUO Shu-ren* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 33 . compound 5b C136H202N8O8S40 ÏàËÆ¶È:68.4% European Journal of Organic Chemistry 2012 1138-1146 Tetrakis(tetrathiafulvalene¨Ctetrathiacrown ether)porphyrazine Triads: Synthesis, Photophysical, and Electrochemical Properties Ruibin Hou, Bao Li, Keli Zhong, Hongda Li, Long-Yi Jin and Bingzhu Yin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 34 . 7¦Á-Methoxyestra-1,3,5(10)-trien-3-ol-17-one C19H24O3 ÏàËÆ¶È:68.4% Steroids 2012 77 1123-1132 Novel 7¦Á-alkoxy-17¦Á-(4¡ä-halophenylethynyl)estradiols as potential SPECT/PET imaging agents for estrogen receptor expressing tumours: Synthesis and binding affinity evaluation Carina Neto, Maria Cristina Oliveira, Lurdes Gano, Fernanda Marques, Takumi Yasuda, Thies Thiemann, Torsten Kniess, Isabel Santos Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 35 . 6-(n-Butylamino) 1-Deoxy-6-demethoxybostrycin C19H23NO6 ÏàËÆ¶È:68.4% Marine Drugs 2012 10 2715-2728 Synthesis and Antitumor Activities of Derivatives of the Marine Mangrove Fungal Metabolite Deoxybostrycin Hong Chen, Xun Zhu, Li-Li Zhong, Bing Yang, Jia Li, Jue-Heng Wu, Sheng-Ping Chen, Yong-Cheng Lin, Yuhua Long and Zhi-Gang She Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 36 . (4S)-3[(2'S,3'R)-2'-Methyl-3'-hydroxydecanoyl)-4-phenyl-methyl-2-oxazolidinone C21H31NO4 ÏàËÆ¶È:68.4% Bioorganic & Medicinal Chemistry 1999 7 737-747 Total synthesis and conformational studies of hapalosin, N-desmethylhapalosin and 8-Deoxyhapalosin Björn Wagner, Gabriel Islas Gonzalez, Marie Elise Tran Hun Dau, Jieping Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 37 . Ibogaine C20H26N2O ÏàËÆ¶È:65% Chemistry of Natural Compounds 2008 44 675-678 INDOLE ALKALOIDS FROM Ervatamia flabellformia Shuang Liang, Haisheng Chen, Li Jin,Weidong Xuan, and Wei-Dong Zhang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 38 . ibogaine ÏàËÆ¶È:65% China Journal of Chinese Materia Medica 2007 32 1296-1299 Study on chemical constituents in rhigome of Ervatamia hainanensis LIANG Shuang, CHENG Haisheng, JIN Yongsheng, JIN Li, LU Jia, DU Jingling Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 39 . 1-O-methyl-5-(2-hydroxytridecyl)resorcinol ÏàËÆ¶È:65% Phytochemistry 1997 44 1559-1563 5-alkylresorcinols from Ononis natrix Librada M. Cañedo, Jose M. Miguel del Corral, Arturo san Feliciano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 40 . ibogaine ÏàËÆ¶È:65% Phytochemistry 1991 30 3785-3792 Alkaloids from leaves and root bark ofErvatamia hirta Pascale Clivio, Bernard Richard, Jean-Robert Deverre, Thierry Sevenet, Monique Zeches, Louisette Le Men-Oliver Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 41 . ibogaine ÏàËÆ¶È:65% Helvetica Chimica Acta 1976 59 2437-2442 13C-NMR. Spectroscopy of Naturally Occurring Substances. XLV. Iboga Alkaloids Ernest Wenkert, David W. Cochran, Hugo E. Gottlieb, Edward W. Hagaman, Raimundo Braz Filho, Francisco Jos¨¦ de Abreu Matos and Maria Iracema Lacerda Machado Madruga Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 42 . 2-{1-[(4-Chlorophenyl)carbonyl]-5-methoxy-2-methyl-1H-indol-3-yl}acetic acid 1-adamantyl ester C29H30O4NCl ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry 2011 19 3242-3248 Synthesis and evaluation of carbaborane derivatives of indomethacin as cyclooxygenase inhibitors Matthias Scholz,Anna L. Blobaum, Lawrence J. Marnett , Evamarie Hey-Hawkins Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 43 . Methyl 4-O-benzyl-3-heptylamino-6-C-methyl-2,3,6-trideoxy-¦Á-D-arabino-hexopyranoside C22H37NO3 ÏàËÆ¶È:65% Canadian Journal of Chemistry 2005 83 801-811 Design and synthesis of oxazolidinone ketolide antibiotic segment mimetics1 Stephen Hanessian and Kiran Kumar Kothakonda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 44 . haplomitrenolide B C20H34O5 ÏàËÆ¶È:65% Phytochemistry 1990 29 585-589 Phytane-and labdane-type diterpenoids from the liverwort Haplomitrium mnioides Yoshinori Asakawa,Masao Toyota,Toru Masuya Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 45 . 3¦Â-angeloyloxy-6¦Â-hydroxy-8¦Â-methoxyeremophil-7(11)-en-12,8¦Á-olide C21H30O6 ÏàËÆ¶È:65% Heterocycles 2003 60 373-378 Three New Eremophilenolides from Ligularia hiberniflorum (Makino) Kitam. Munehiro Nakatani,* Saori Maeda, Kenji Higashi, Junichi Kurawaki, Hiroaki Okamura, and Tetsuo Iwagawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 46 . ibogaine ÏàËÆ¶È:65% Phytochemistry 1984 23 175-178 13C NMR analysis of alkaloids from peschiera fuchsiaefolia Raquel M. Braga, Hermogenes F. Leit¨¢o Filho, Francisco De A.M. Reist Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 47 . 6-hexyloxy-1-oxo-3-benzylisoindoline-4,5-dicarbonitrile C23H23N3O2 ÏàËÆ¶È:65% Heterocycles 2001 55 1663-1678 Synthesis of 3-Substituted Isoindolin-1-ones by Regioselective Cyclization of Nitrile with a Styryl Double Bond Fen-Tair Luo* and Chin-Hsin Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 48 . (1E,4Z,6E)-5-hydroxy-1,7-bis(3-methoxy-4-(octyloxy)phenyl)-hepta-1,4,6-trien-3-one ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry 2010 18 1591-1598 Binding of curcumin and its long chain derivatives to the activator binding domain of novel protein kinase C Anjoy Majhi, Ghazi M. Rahman, Shyam Panchal, Joydip Das Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 49 . methyl 2,4-dideoxy-3-O-benzoyl-4-C-(2Z-octenyl)-¦Á-D-arabino-hexopyranoside ÏàËÆ¶È:65% Russian Journal of Organic Chemistry 2003 39 658-662 Prostanoids: LXXXV. Synthesis 9-Oxo Derivatives of 9-LO Thromboxans R. R. Akhmetvaleev, R. V. Bikbulatov, T. A. Belogaeva, F. A. Akbutina and M. S. Miftakhov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 50 . (S)-1-[(2R,4S,6R)-6-heptyl-2-phenyl-1,3-dioxan-4-yl]pent-4-en-2-ol C22H34O3 ÏàËÆ¶È:65% European Journal of Organic Chemistry 2011 6781-6788 Stereoselective Total Synthesis of Polyrhacitides A and B J. S. Yadav and Goreti Rajendar Structure 13C NMR ̼Æ×Ä£Äâͼ |
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