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13C NMR (125MHz, CD3OD) 16.6,24.7,26.1,27.6,29.6,31.2,34.2,38.1,52.7,53.4,63.4,75.4,82.9,128.2,137.5 |
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1 . alismorientol A C15H28O4 ÏàËÆ¶È:73.3% Chemical & Pharmaceutical Bulletin 2007 55(6) 905-907 Two New Sesquiterpenes from Alisma orientalis Zhi-Yong JIANG,Xue-Mei ZHANG,Jun ZHOU,Feng-Xue ZHANG,Ji-Jun CHEN,Yang L¨¹,Li WU,and Qi-Tai ZHENG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . (-)-norrotundene C14H22 ÏàËÆ¶È:73.3% Phytochemistry 2001 58 799-810 Chemical study of the essential oil of Cyperus rotundus Mesmin Mekem Sonw, Wilfried A. König Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . sophorbenzamine C22H26N20 ÏàËÆ¶È:73.3% Chemistry of Natural Compounds 1996 32 737-858 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter 2, continued R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 8-oxoguaioxide ÏàËÆ¶È:73.3% Phytochemistry 1999 51 757-760 The hydroxylation of the sesquiterpenoid guaioxide by Mucor plumbeus Simone Fontes Arantes, James R. Hanson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . floridimine ÏàËÆ¶È:73.3% Phytochemistry 1997 46 845-853 Bioactive saturated pyrrolizidine alkaloids from Heliotropium floridum M. Reina, A. Gonzalez-Coloma, C. Gutierrez, R. Cabrera, J. Henriquez, L. Villarroel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (-)-1,12-Oxaguai-10(15)-ene C15H24O ÏàËÆ¶È:73.3% Phytochemistry 1995 40 1159-1162 (− -1, 12-oxagual-10(15)-ene: A sesquiterpene from Eriostemon fitzgeraldiiSatyajit D. Sarker, James A. Armstrong, Peter G. Waterman Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . N-õ£»ùÉñ¾Çʰ·´¼ ÏàËÆ¶È:73.3% Chinese Journal of Marine Drugs 1995 2 1-4 SIX KINDS OF N-ACYLSPHINGOSINES FROM THE CHINESE GORGONIA JUNCEELLA SQUAMATA Lin Yongcheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . Capillosanol C15H24O ÏàËÆ¶È:73.3% Organic Letters 2009 Vol.11,No.21 4830-4833 New Terpenoids from the Soft Corals Sinularia capillosa and Nephthea chabroli Shi-Yie Cheng, Ki-Jhih Huang, Shang-Kwei Wang, Zhi-Horng Wen,Chi-Hsin Hsu, Chang-Feng Dai, and Chang-Yih Duh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . alloromadendrane-4¦Â,10¦Á-diol C15H26O2 ÏàËÆ¶È:73.3% Phytochemistry 1987 26 1059-1063 Sesquiterpene lactones and a sesquiterpene diol from jamaican ambrosia peruviana Gwendolyn Goldsby,Basil A. Burke Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . compound 4 ÏàËÆ¶È:73.3% Pharmazie 2002 57 778-779 New illudane sesquiterpenes from the basidiomycete Clitocybe rivulosa HKI 0273 B. Schlegel - U. Luhmann - T. T. Kiet - E. Leistner - U. Gräfe Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . Junicedranol C15H26O ÏàËÆ¶È:73.3% Tetrahedron Letters 1995 36 6347-6350 Junicedranol, a sesquiterpene with a novel carbon skeleton from Juniperus oxycedrus ssp. macrocarpa Alejandro F. Barrero, Enrique Alvarez-Manzaneda, Armando Lara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Junicedranol C15H26O ÏàËÆ¶È:73.3% Tetrahedron Letters 1995 36 6347-6350 Junicedranol, a sesquiterpene with a novel carbon skeleton from Juniperus oxycedrus ssp. macrocarpa Alejandro F. Barrero, Enrique Alvarez-Manzaneda, Armando Lara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (R)-MTPA ester ÏàËÆ¶È:73.3% Tetrahedron Letters 1995 36 6347-6350 Junicedranol, a sesquiterpene with a novel carbon skeleton from Juniperus oxycedrus ssp. macrocarpa Alejandro F. Barrero, Enrique Alvarez-Manzaneda, Armando Lara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (S)-2-(4-chlorobenzylideneamino)-3-hydroxy-N-tetradecylpropanamide C24H39ClN2O2 ÏàËÆ¶È:73.3% Bioorganic & Medicinal Chemistry 2010 18 5316-5322 Novel anti-viability ceramide analogs: Design, synthesis, and structure¨Cactivity relationship studies of substituted (S)-2-(benzylideneamino)-3-hydroxy-N-tetradecylpropanamides Jiawang Liu, James W. Antoon, Adharsh Ponnapakkam, Barbara S. Beckman, Maryam Foroozesh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 8 C16H32O2Si ÏàËÆ¶È:73.3% Canadian Journal of Chemistry 1997 75 634-640 Isolation, structure, and synthesis of chenopodanol and the absolute configuration of chenopodene and chenopodanol Motoo Tori, Tomonobu Hamaguchi, Mamiko Aoki, Masakazu Sono, Yoshinori Asakawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 14-dehydroxyl daucucarotol C15H28O2 ÏàËÆ¶È:73.3% Chinese Science Bulletin 2013 58 1115-1119 New terpenoids from the roots of Jatropha curcas YANG YuanFeng, LIU JieQing, LI XuYang, LIU EnQian, LI ZhongRong, QIU MingHua Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Agrocybin H C15H26O2 ÏàËÆ¶È:73.3% Natural Products and Bioprospecting 2012 2 130-132 Two novel fomannosane-type sesquiterpenoids from the culture of the basidiomycete Agrocybe salicacola Liang-Yan Liu, Zheng-Hui Li, Ze-Jun Dong, Xing-Yao Li, Jia Su, Yan Li, Ji-Kai Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . N-Methoxy (3R,4R,5S)-4-acetamido-5-amino-3-(1-ethylpropoxy)-1-cyclohexenecarboxamide C15H27N3O4 ÏàËÆ¶È:73.3% Bioorganic & Medicinal Chemistry 2014 22 6647-6654 Oseltamivir hydroxamate and acyl sulfonamide derivatives as influenza neuraminidase inhibitors Bei-Tao Hong, Chun-Lin Chen, Jim-Min Fang, Keng-Chang Tsai, Shi-Yun Wang, Wen-I Huang, Yih-Shyun E. Cheng, Chi-Huey Wong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . (2R*,3aR*,6R*)-methyl 6-(4-methoxyphenyl)-2,6-dimethylhexahydropyrrolo[1,2-b]isoxazole-2-carboxylate C17H23NO4 ÏàËÆ¶È:73.3% Tetrahedron 2014 70 6384-6391 Synthesis of 5-alkyl-5-aryl-1-pyrroline N-oxides from 1-aryl-substituted nitroalkanes and acrolein via Michael addition and nitro reductive cyclization Jingjing Xu, Xingyao Li, Jinlong Wu, Wei-Min Dai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . ¦Â-cedrol ÏàËÆ¶È:73.3% Chemistry of Natural Compounds 1985 21 38-41 Mono- and sesquiterpenoids of the oleoresin of Abies nephrolepis. Crystal structure of (+)-¦Â-cedrol V. A. Khan, N. A. Pankrushina, Yu. V. Gatilov, I. Yu. Bagryanskaya, Zh. V. Dudovenko, V. A. Pentegova Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
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-1, 12-oxagual-10(15)-ene: A sesquiterpene from Eriostemon fitzgeraldii