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̼Æ×Êý¾ÝÈçÏ£º PVA 14.16, 14.23, 14.26, 19.76, 22.72, 22.76, 22.79, 22.82, 23.23, 26.77, 27.16, 29.02, 29.23, 29.78, 29.87, 30.11, 30.20, 30.23, 32.00, 32.03, 32.82, 33.44, 33.53, 33.75, 33.89, 37.17, 37.44, 37.51, 76.77, 77.02, 77.28 |
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1 . 8,10,13-Trimethyltetradecanoic acid (2E)-3-methylhexadec-2-enyl ester (tomentosate) C34H66O2 ÏàËÆ¶È:64.7% Natural Product Communications 2012 7 63-64 A New Long-Chain Unsaturated Ester and Other Constituents of Hypericum tomentosum Ouassila Touafek, Zahia Kabouche*, Joël Boustie and Christian Bruneau Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 5,13-Dimethyl-5-heptadecen-1-ol ÏàËÆ¶È:64.5% Bioscience, Biotechnology, and Biochemistry 2009 73 1618-1622 Synthesis and Field Evaluation of Methyl-branched Ketones, Sex Pheromone Components Produced by Lithosiinae Female Moths in the Family of Arctiidae Nguyen Duc DO, Masakatsu KINJO, Tomonori TAGURI, Yasushi ADACHI, Rei YAMAKAWA and Tetsu ANDO Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-giganin C35H64O6 ÏàËÆ¶È:64.5% Angewandte Chemie International Edition 2013 52 2503-2506 Stereoselective Total Synthesis of (+)-Giganin and Its C10 Epimer by Using Late-Stage Lithiation¨CBorylation Methodology Catherine J. Fletcher, Dr. Katherine M. P. Wheelhouse and Prof. Varinder K. Aggarwal Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . palmitate C36H70O2 ÏàËÆ¶È:64.5% Natural Product Communications 2011 6 767-772 Lipophilic Components from the Ecuadorian Plant Schistocarpha eupatorioides Gianluca Gilardoni, Solveig Tosi, Giorgio Mellerio, Maria Elena Maldonado, Ximena Chiriboga and Giovanni Vidari Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . suillumide C33H65NO4 ÏàËÆ¶È:61.2% Chemistry & Biodiversity 2008 Vol. 5 120-125 A New Ceramide from Suillus luteus and Its Cytotoxic Activity against Human Melanoma Cells Francisco Le¨®n, Ignacio Brouard, Fernando Torres, Jos¨¦ Quintana, Augusto Rivera, Francisco Est¨¦vez, and Jaime Bermejo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . balansenate I C32H62O2 ÏàËÆ¶È:61.2% Helvetica Chimica Acta 2003 Vol. 86 2452 New Long-Chain Esters and Adenine Analogs from the Leaves of Formosan Bridelia balansae Yeh-Hsin Tsai, Ih-Sheng Chen, and Ian-Lih Tsai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . penasulfate A C36H67NO11S2Na ÏàËÆ¶È:61.2% Journal of Natural Products 2004 67 1346-1350 Penasulfate A, a New ¦Á-Glucosidase Inhibitor from a Marine Sponge Penares sp. Yoichi Nakao, Takashi Maki, Shigeki Matsunaga, Rob W. M. van Soest, and Nobuhiro Fusetani Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-hydroxy-25-desoxyneorollinic C37H66O7 ÏàËÆ¶È:61.2% Journal of Natural Products 1989 Vol 52 822 4-Hydroxy-25-desoxyneorollinicin, a New Bistetrahydrofuranoid Acetogenin from Rollinia papilionella Milton J. Abreo, Albert T. Sneden Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . trans-phytyl palmitate C16H31O ÏàËÆ¶È:61.2% Journal of Natural Products 1991 Vol 54 1444 Diterpene Fatty Acid Ester from Leucas nutans Mashooda Hasan, Dadu Khan Burdi, Viqar Uddin Ahmad Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . [(1S,2S)-1-(16-bromohexadecyl)-2-methyleicosyl-oxy]-tert-butyldimethylsilane C43H89BrOSi ÏàËÆ¶È:61.2% Tetrahedron 2013 69 6285-6296 The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 8-{(1S,2R)-2-[(1S,20S,21S)-20-(tert-butyldimethylsilanyloxy)-1,21-dimethylnonatriacontyl]-cyclopropyl}-octan-1-ol C58H118O2Si ÏàËÆ¶È:61.1% Tetrahedron 2013 69 6285-6296 The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . montanacin C37H68O8 ÏàËÆ¶È:60.6% Tetrahedron Letters 1990 31 1861-1864 Deux nouvelles acetogenines monotetrahydrofuranniques cytotoxiques: L'annomonicine et la montanacine Akino Jossang, B¨¦atrice Dubaele, Andr¨¦ Cav¨¦, Marie-H¨¦l¨¨ne Bartoli, H¨¦l¨¨ne Beriel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . (R)-2-{(R)-1-hydroxy-17-[(1S,2R)-2-((1S,20S,21S)-20-hydroxy-1,21-dimethylnonatriacontyl)-cyclopropyl]-heptadecyl}-hexacosanoic acid C87H172O4 ÏàËÆ¶È:60.6% Tetrahedron 2013 69 6285-6296 The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . C10-epi-giganin C35H64O6 ÏàËÆ¶È:60.6% Angewandte Chemie International Edition 2013 52 2503-2506 Stereoselective Total Synthesis of (+)-Giganin and Its C10 Epimer by Using Late-Stage Lithiation¨CBorylation Methodology Catherine J. Fletcher, Dr. Katherine M. P. Wheelhouse and Prof. Varinder K. Aggarwal Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . cus-2 ÏàËÆ¶È:59.3% Chemical & Pharmaceutical Bulletin 1996 44 481-485 Resin Glycosides. XXIII. Two Novel Acylated Trisaccharides Related to Resin Glycoside from the Seeds of Cuscuta chinensis Kazumoto MIYAHARA,Xiao-ming DU,Minae WATAMABE,Chizuko SUGIMURA,Shoji YAHARA and Toshihiro NOHARA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . (2R)-2-((1R)-1-(tert-butyldimethylsilyloxy)-17-(2-((2S,21S,22S)-22-methyl-21-(tetrahydro-2H-pyran-2-yloxy)tetracontan-2-yl)cyclopropyl)heptadecyl)hexacosanoic acid C98H194O5Si ÏàËÆ¶È:59.3% Tetrahedron 2013 69 6285-6296 The synthesis of methoxy and keto mycolic acids containing methyl-trans-cyclopropanes Gani Koza, Maged Muzael, Richard R. Schubert-Rowles, Cornelia Theunissen, Juma'a R. Al Dulayymi, Mark S. Baird Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Merocyclophane B ÏàËÆ¶È:59.3% Phytochemistry 2012 79 109-115 Merocyclophanes A and B, antiproliferative cyclophanes from the cultured terrestrial Cyanobacterium Nostoc sp. Hahk-Soo Kang, Bernard D. Santarsiero, Hyunjung Kim, Aleksej Krunic, Qi Shen, Steven M. Swanson, Heebyung Chai, A. Douglas Kinghorn, Jimmy Orjala Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

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