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1 . Oxyphyllone E ÏàËÆ¶È:93.3% Chinese Journal of Natural Medicines 2010 8 2011-6-8 Two New Norsesquiterpenes from the Fruits of Alpinia oxyphylla XU Jun-Ju; TAN Ning-Hua; ZENG Guang-Zhi; HAN Hong-Jin; PENG Yong-Fang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 6-epi-¦Á-cubebene C15H24 ÏàËÆ¶È:66.6% Phytochemistry 2002 59 805-810 epi-Cubebanes from Solidago canadensis Adeleke A. Kasali, Olusegun Ekundayo, Claudia Paul, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (¡À)-(1R*,11R*,12S*)-12-hydroxy-1-nitrobicyclo[9.3.1]pentadecan-15-one ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2011 2101-2110 A General, Diastereoselective Synthesis of Highly Functionalized Bicyclo[n.3.1]alkane Systems Based on an Anionic Domino Reaction of -Nitrocycloalkanones Giorgio Giorgi, Sonia Miranda, Miriam Ruiz, Jean Rodriguez, Pilar L¨®pez-Alvarado and J. Carlos Men¨¦ndez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . anthosterone B ÏàËÆ¶È:60% Journal of Natural Products 2004 67 731-733 Phorbasterones A−D, Cytotoxic Nor-Ring A Steroids from the Sponge Phorbas amaranthus Makoto N. Masuno, Joseph R. Pawlik, and Tadeusz F. Molinski Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . eudesmandiol C15H28O2 ÏàËÆ¶È:60% Phytochemistry 1989 28 936-938 A eudesmanediol from Cymbopogon distans C.S. Mathela,A.B. Melkani,Alka Pant,Vasu Dev,Thomas E. Nelson,Hakon Hope,Albert T. Bottini Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . isocaespitol ÏàËÆ¶È:60% Tetrahedron letters 1979 20 2719-2722 Carbon-13 NMR application to Laurencia polyhalogenated sesquiterpenes A.G. Gonz¨¢lez, J.D. Mart¨ªn, V.S. Mart¨ªn, M. Norte Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . compound 9b C15H24O2 ÏàËÆ¶È:60% Bulletin of the Chemical Society of Japan 1993 66 2694-2699 Synthetic Photochemistry. LXI. A Total Synthesis of (¡À)-Valeranone, a cis-Decalone Sesquiterpenoid from Valeriana officinalis, via an Intramolecular Photocycloaddition Hitoshi Takeshita, Ying-She Cui, Nobuo Kato, Akira Mori Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 4e C30H54Pd2 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2012 1945-1952 Development of the First Menthane-Based Chiral Bis(¦Ð-allylpalladium) Catalysis: Asymmetric Allylation of Imines Rodney A. Fernandes and Dipali A. Chaudhari Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (+)-myrionamide C15H24N2O ÏàËÆ¶È:60% The Journal of Organic Chemistry 2008 73 7565-7573 Structure and Total Synthesis of (− -Myrionidine and (− -Schoberine, Antimalarial Alkaloids from Myrioneuron nutansVan Cuong Pham, Akino Jossang, Philippe Grellier, Thierry Sevenet, Van Hung Nguyen and Bernard Bodo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . ishwarane ÏàËÆ¶È:60% Australian Journal of Chemistry 1994 47 587-607 Constituents of Some Species of Beilschmiedia and Endiandra (Lauraceae): New Endiandric Acid and Benzopyran Derivatives Isolated From B. oligandra JE Banfield, DS Black, DJ Collins, BPM Hyland, JJ Lee and SR Pranowo Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-04-15 07:11:11
nkx1979
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µÚ¶þ¸ö 1 . 7-O-(¦Â-D-glucopyranosyl)chrysin ÏàËÆ¶È:89.4% Molecules 2004 9 568-573 Flavone Glycosides from Calycotome Villosa Subsp. Intermedia Ali E. Antri, Ibtissam Messouri, Rachida C. Tlemçani, Mohamed Bouktaib, Rachid El Alami, Brahim El Bali and Mohammed Lachkar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . °×ÑîËØ7-O-¦Â-D-ÆÏÌÑÌÇÜÕ ÏàËÆ¶È:89.4% Chinese Traditional and Herbal Drugs 2009 40 196-199 ºìÈÞëÑòÌã¼×ÖеĻÆÍªÀà³É·Ö ÉÐСÑÅ;Àî˧;ÍõËØ¾ê;ÑîÓÀ´º;ʯ½¨¹¦ Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . aequinoctin ÏàËÆ¶È:89.4% Chinese Pharmaceutical Journal 2011 46 170-173 Flavonoids from the Seeds of Oroxylum indicum (L.) Vent WEN Jing-bing, ZHANG Qing-wen, YIN Zhi-qi, LI Ya-ping, HAN Xiao-wen, YE Wen-cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . chrysin 7-glucoside ÏàËÆ¶È:88.8% Phytochemistry 1983 22 2323-2324 Chrysin 7-gentiobioside from the flowers of spartium junceum Salvatore De Rosa, salvatore De Stefano Structure 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2013-04-15 07:13:09
nkx1979
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µÚÈý¸ö 1 . (4aS,8aR)-5,5,8a-trimethyl-3-oxo-3,4,4a,5,6,7,8,8a-octahydronaphthalene-2-carbaldehyde C14H20O2 ÏàËÆ¶È:64.2% Magnetic Resonance in Chemistry 2007 45 993-996 LTA-mediated synthesis and complete assignment of 1H and 13C NMR data of two natural 11-nordrimanes: isonordrimenone and polygonone (pages 993¨C996) Luis Moreno-Osorio, Luis Espinoza, Mauricio Cuellar and Marcelo Preite Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (E)-3,7,11-trimethyldodeca-2,10-dien-1-ol C15H28O ÏàËÆ¶È:64.2% Bioorganic & Medicinal Chemistry 2010 18 3116-3124 Structure¨Cactivity relationships in the conversion of vitamin K analogues into menaquinone-4. Substrates essential to the synthesis of menaquinone-4 in cultured human cell lines Yoshitomo Suhara, Akimori Wada, Yoji Tachibana, Masato Watanabe, Kanae Nakamura, Kimie Nakagawa, Toshio Okano Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound C14H24O2 ÏàËÆ¶È:64.2% Journal of the American Chemical Society 2008 130 11114-11121 Total Synthesis, Revised Structure, and Biological Evaluation of Biyouyanagin A and Analogues Thereof K. C. Nicolaou, T. Robert Wu, David Sarlah, David M. Shaw, Eric Rowcliffe and Dennis R. Burton Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 2-methylcyclopentanenitrile C7H11N ÏàËÆ¶È:64.2% Journal of Medicinal Chemistry 1994 37 275-286 alpha.-Spirocyclopentyl- and .alpha.-spirocyclopropyl-.gamma.-butyrolactones: conformationally constrained derivatives of anticonvulsant and convulsant .alpha.,.alpha.-disubstituted .gamma.-butyrolactones Eileen M. Peterson, Kun Xu, Katherine D. Holland, Ann C. McKeon, Steven M. Rothman, James A. Ferrendelli, Douglas F. Covey Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . 1-isocyanoaromadendrane ÏàËÆ¶È:64.2% Bulletin des Soci¨¦t¨¦s Chimiques Belges 1987 96 539-543 I-Isocyanoaromadendrane, A New Isonitrile Sesquiterpene from the Sponge Acanthella Acuta J. C. Braekman, D. Daloze, F. Deneubourg, J. Huysecom and G. Vandevyver Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . Nardoaristolone B C14H18O2 ÏàËÆ¶È:64.2% Organic Letters 2013 15 1000-1003 Nardoaristolones A and B, Two Terpenoids with Unusual Skeletons from Nardostachys chinensis Batal Ming-Li Liu, Ying-Hui Duan, Yun-Long Hou, Chang Li, Hao Gao, Yi Dai, and Xin-Sheng Yao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . androst-4-en-3-one ÏàËÆ¶È:63.1% Phytochemistry 1996 42 411-415 The hydroxylation of testosterone and some relatives by Cephalosporium aphidicola James R. Hanson, Habib Nasir, Aslam Parvez Structure 13C NMR ̼Æ×Ä£Äâͼ |

4Â¥2013-04-15 07:15:22
nkx1979
ľ³æ (ÕýʽдÊÖ)
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- רҵ: ÌìȻҩÎﻯѧ
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µÚËĸö 1 . 11-hydroxy-valenc-1(10)-en-2-one C15H24O2 ÏàËÆ¶È:93.3% Phytochemistry 1987 26 571-572 A valencane sesquiterpenoid from Teucrium carolipaui Giuseppe Savona,Franco Piozzi,Mar¨ªa C. De La Torre,Orietta Servettaz,Benjam¨ªn Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (+)-(4R,5S,7R)-7,11,12-Trihydroxynootkatone C15H24O4 ÏàËÆ¶È:73.3% Bioorganic & Medicinal Chemistry 2011 19 2464-2469 Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 11 ÏàËÆ¶È:66.6% Journal of Natural Products 1997 60 1026-1030 Sesquiterpene Glycosides and Phenylpropanoid Esters from Phonus arborescens (Carthamus arborescens) Alejandro F. Barrero, Pilar Arteaga, Jos¨¦F. Qu¨ªlez, Ignacio Rodr¨ªguez, and M. Mar Herrador Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 12 ÏàËÆ¶È:66.6% Phytochemistry 1994 37 1101-1107 Sesquiterpene lactones, lignans and aromatic esters from Cheirolophus species J.Alberto Marco, Juan F. Sanz-Cervera, Vicente Garcia-Lliso, Alfonso Susanna, Nuria Garcia-Jacas Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (+)-nootkatone ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2011 19 2464-2469 Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (+)-(4R,5S,7R)-13-Hydroxynootkatone ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2011 19 2464-2469 Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (+)-(4R,5S,7R)-11,12-Dihydroxynootkatone ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2011 19 2464-2469 Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . nootkatone ÏàËÆ¶È:66.6% Phytochemistry 1987 26 571-572 A valencane sesquiterpenoid from Teucrium carolipaui Giuseppe Savona,Franco Piozzi,Mar¨ªa C. De La Torre,Orietta Servettaz,Benjam¨ªn Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . Nootkatone ÏàËÆ¶È:66.6% Journal of Agricultural and Food Chemistry 2000 48 3639-3641 Insecticidal Sesquiterpene from Alpinia oxyphylla against Drosophila melanogaster Mitsuo Miyazawa, Yuji Nakamura, and Yukio Ishikawa Structure 13C NMR ̼Æ×Ä£Äâͼ |

5Â¥2013-04-15 07:17:33
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×îºóÒ»¸ö 1 . (+)-(4R,5S,7R)-13-Hydroxynootkatone ÏàËÆ¶È:100% Bioorganic & Medicinal Chemistry 2011 19 2464-2469 Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (+)-nootkatone ÏàËÆ¶È:80% Bioorganic & Medicinal Chemistry 2011 19 2464-2469 Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . nootkatone ÏàËÆ¶È:80% Phytochemistry 1987 26 571-572 A valencane sesquiterpenoid from Teucrium carolipaui Giuseppe Savona,Franco Piozzi,Mar¨ªa C. De La Torre,Orietta Servettaz,Benjam¨ªn Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Nootkatone ÏàËÆ¶È:80% Journal of Agricultural and Food Chemistry 2000 48 3639-3641 Insecticidal Sesquiterpene from Alpinia oxyphylla against Drosophila melanogaster Mitsuo Miyazawa, Yuji Nakamura, and Yukio Ishikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . (+)-(4R,5S,7R)-11,12-Dihydroxynootkatone ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2011 19 2464-2469 Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (+)-(4R,5S,7R)-7,11,12-Trihydroxynootkatone C15H24O4 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2011 19 2464-2469 Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites Anna Gliszczy¨½ska, Agnieszka Łysek, Tomasz Janeczko, Marta Świtalska,Joanna Wietrzyk, Czesław Wawrze¨½czyk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 11-hydroxy-valenc-1(10)-en-2-one C15H24O2 ÏàËÆ¶È:60% Phytochemistry 1987 26 571-572 A valencane sesquiterpenoid from Teucrium carolipaui Giuseppe Savona,Franco Piozzi,Mar¨ªa C. De La Torre,Orietta Servettaz,Benjam¨ªn Rodr¨ªguez Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 3 ÏàËÆ¶È:60% Chemical Communications 1977 27-28 Vetispirane sesquiterpene glucosides from flue-cured virginia tobacco: structure, absolute stereochemistry, and synthesis. X-Ray structure of the p-bromobenzenesulphonate of one of the derived aglycones Robert C. Anderson, Donald M. Gunn, Judith Murray-Rust, Peter Murray-Rust and James S. Roberts Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 13-hydroxy-3,11-(7¦ÁH,10¦ÂH)-acordien-3-one C15H22O2 ÏàËÆ¶È:60% Journal of Chemical Research 2007 31 38-39 A new sesquiterpene from the seeds of Physalis alkekengi L. var. franchi Zhan, Zha-Jun; Li, Cheng-Ping; Shan, Wei-Guang Structure 13C NMR ̼Æ×Ä£Äâͼ |

6Â¥2013-04-15 07:19:24














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-Myrionidine and (−