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1 . eujavanicol A C19H32O4 ÏàËÆ¶È:73.6% Journal of Natural Products 2007 70 1510-1512 Eujavanicols A¨CC, Decalin Derivatives from Eupenicillium jaWanicum Shou Nakadate,Koohei Nozawa,Hitoshi Horie, Yuichi Fujii, Masahiro Nagai, Tomoo Hosoe,Ken-ichi Kawai,Takashi Yaguchi, and Kazutaka Fukushima Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . eujavanicol A C19H32O4 ÏàËÆ¶È:73.6% Chemistry of Natural Compounds 2009 45 753-755 DEHYDRODECALIN DERIVATIVE FROM MARINEISOLATE OF THE FUNGUS Wardomyces inflatus O. F. Smetanina, A. I. Kalinovskii, A. A. Kicha,A. N. Yurchenko M. V. Pivkin,and T. A. Kuznetsova Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . 6¦Â-Hydroxy-15,16-epoxy-labda-8,13(16),14-trien-7-one C20H28O3 ÏàËÆ¶È:65% Phytochemistry 1995 40 875-879 Persianone, a dimeric diterpene from Ballota aucheri A. Rustaiyan, M. H. Mosslemin-Kupaii, F. Papastergiou, J. Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 8¦Á,13-dihydroxy-labda-6,14-diene C20H32O ÏàËÆ¶È:65% Phytochemistry 1991 30 3683-3691 Seco-, nor-, normal and rearranged labdanes fromHaplopappus parvifolius C. Zdero, F. Bohlmann, H.M. Niemeyer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 6-oxo-14,15-nor-labda-7-ene C18H28O2 ÏàËÆ¶È:65% Phytochemistry 1991 30 3683-3691 Seco-, nor-, normal and rearranged labdanes fromHaplopappus parvifolius C. Zdero, F. Bohlmann, H.M. Niemeyer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 3-hydroxy-19-oxo-ent-labda-8(17),13-dien-16,15-olide C20H28O4 ÏàËÆ¶È:65% Fitoterapia 2012 83 1506-1513 Quinone reductase (QR) inducers from Andrographis paniculata and identification of molecular target of andrographolide Yonglei Yuan, Long Ji, Liping Luo, Juan Lu, Xiaoqiong Ma, Zhongjun Ma, Zhe Chen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 3,7-dimethyl-1-[2-O-(2-methylbutyroyl)-3-O-acetyl-¦Â-D-xylopyranosyloxy]-6-octene C22H38O7 ÏàËÆ¶È:63.6% Phytochemistry 1988 27 517-522 Terpenoid and flavone constituents of Polemonium viscosum Donald B. Stierle,Andrea A. Stierle,R.D. Larsen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . eujavanicol B C19H32O4 ÏàËÆ¶È:63.1% Journal of Natural Products 2007 70 1510-1512 Eujavanicols A¨CC, Decalin Derivatives from Eupenicillium jaWanicum Shou Nakadate,Koohei Nozawa,Hitoshi Horie, Yuichi Fujii, Masahiro Nagai, Tomoo Hosoe,Ken-ichi Kawai,Takashi Yaguchi, and Kazutaka Fukushima Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (3R,4S,5R,7S,9R)-3-hydroxy-9-isobutanoyloxysolavetivone C19H28O4 ÏàËÆ¶È:63.1% Journal of Natural Products 1998 61 1516-1519 Phytoalexins from Hairy Roots of Hyoscyamus albus Treated with Methyl Jasmonate Masanori Kuroyanagi, Takeshi Arakawa, Yoji Mikami, Kenichi Yoshida, Nobuo Kawahar, Tatsuo Hayashi, and Hidehiko Ishimaru Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (10R)-12-acetoxy-1-oxo-13,14,15,16-tetranor-ent-haliman-18-oate C19H30O5 ÏàËÆ¶È:63.1% Molecules 2006 11 792-807 Synthetic Studies Towards the ent-Labdane Diterpenoids: Rearrangement of ent-Halimanes Isidro S. Marcos, Mar¨ªa J. Sexmero, Felix A. Hern¨¢ndez, Marta Corrales, Pilar Basabe, David D¨ªez and Julio G. Urones Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 1¦Á-acetoxyeudesm-4-en-6¦Â,11¦ÂH-12,6-olide ÏàËÆ¶È:63.1% Phytochemistry 1994 37 477-485 Sesquiterpene lactones from North African Artemisia species J.Alberto Marco, Juan F. Sanz-Cervera, Jose M. Pareja, Felix Sancenon, Joan Valles-Xirau Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . torrentin acetate ÏàËÆ¶È:63.1% Phytochemistry 1989 28 2505-2506 Revision of the structure of torrentin J.Alberto Marco,Juan F. Sanz,M. Carda Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 14,15-dinor-7-labden-13-one ÏàËÆ¶È:63.1% Phytochemistry 1990 29 2223-2228 Terpenoid compounds from Parentucellia latifolia J.G. Urones,I.S. Marcos,I. Cubillo,N.Martin Garrido,P. Basabe Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . (20S)-16-Ene-22-thia-24-nor-26,27-dimethyl-8-ol tert-butyldimethylsilyl ether C24H46O2SSi ÏàËÆ¶È:63.1% Bioorganic & Medicinal Chemistry 2008 16 1796-1815 Synthesis and structure¨Cactivity relationships of 16-ene-22-thia-1¦Á,25-dihydroxy-26,27-dimethyl-19-norvitamin D3 analogs having side chains of different sizes Hajime Takaku, Yukiko Miyamoto, Shiori Asami, Mika Shimazaki, Sachiko Yamada, Keiko Yamamoto, Nobuyuki Udagawa, Hector F. DeLuca, Masato Shimizu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 16¦Â,17-dihydroxy-7-oxo-ent-atisan-19-al C19H26O4 ÏàËÆ¶È:63.1% Phytochemistry 2010 71 1313-1321 Biotransformation of 7¦Á-hydroxy- and 7-oxo-ent-atis-16-ene derivatives by the fungus Gibberella fujikuroi Braulio M. Fraga, Pedro Gonzalez, Victoria Gonzalez-Vallejo, Ricardo Guillermo, Luz N. Diaz Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . ethyl (-)-(3R,4aS,4bS,8R,8aR,10aR)-3-methyl-9-oxo-1,4a,4b,7,8,8a,9,10a-octahydro-2,4,10-trioxaphenanthrene-8-carboxylate C15H20O6 ÏàËÆ¶È:63.1% European Journal of Organic Chemistry 2011 2789-2800 Synthesis of Naturally Occurring Cyclohexene Rings Using Stereodirected Intramolecular Diels¨CAlder Reactions Through Asymmetric 1,3-Dioxane Tethering Hajer Abdelkafi, Laurent Evanno, Alexandre Deville, Lionel Dubost, Ang¨¨le Chiaroni and Bastien Nay Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . 9¦Á,11-epoxy-androst-4-ene-3,12,17-trione C19H22O4 ÏàËÆ¶È:63.1% Tetrahedron 2012 68 9249-9255 Oxidation of unsaturated steroid ketones with hydrogen peroxide catalyzed by Fe(bpmen)(OTf)2. New methodology to access biologically active steroids by chemo-, and stereoselective processes David Clemente-Tejeda, Alejandro L¨®pez-Moreno, Francisco A. Bermejo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . 18-oxoferruginol C20H28O2 ÏàËÆ¶È:63.1% Tetrahedron 2012 68 9612-9615 Short syntheses of (+)-ferruginol from (+)-dehydroabietylamine Miguel A. Gonz¨¢lez, David P¨¦rez-Guaita Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . N-pivaloyl-(S)-3-methyl-(S)-2-pentylindoline C19H29NO ÏàËÆ¶È:63.1% Tetrahedron 2013 69 2542-2549 Mitsunobu cyclodehydration of N-pivaloyl-2-aminophenethyl alcohol for asymmetric synthesis of trans-2,3-disubstituted indolines Kyoung Hee Kang, Yelim Kim, Chan Im, Yong Sun Park Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 1¦Á-acetoxyeudesm-4-en-6¦ÂH,11¦ÂH-12,6-olide ÏàËÆ¶È:63.1% Natural Medicines 2003 57 114-116 Sesquiterpenoids from Artemisia tenuisecta Kawazoe Kazuyoshi,Morishita Nao,et al. Structure 13C NMR ̼Æ×Ä£Äâͼ |
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