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| 17.83, 22.88, 24.72, 25.24, 27.34, 29.11, 29.16, 32.70, 33.80, 71.21, 73.25, 80.98, 109.37, 171.49, 178.28, 198.35 |
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²éѯ½á¹û£º¹²²éµ½533¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . Dihydropyran C16H26O4 ÏàËÆ¶È:81.2% Journal of Natural Products 1991 Vol 54 396 New Antibiotics from Strains of Trichoderma harzianum Faramak Almassi, Emilio L. Ghisalberti, Melissa J. Narbey, Krishnapillai Sivasithamparam Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound 6 C16H26O4 ÏàËÆ¶È:81.2% Journal of Natural Products 1993 Vol 56 1799 Antifungal Metabolites from Trichoderma harzianum Emilio L. Ghisalberti, Catherine Y. Rowland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . koninginin B ÏàËÆ¶È:81.2% Bioscience, Biotechnology, and Biochemistry 1995 59 1747-1749 Koninginin E : Isolation of a Biologically Active Natural Product from Trichoderma koningii Stephen R. Parker, Horace G. Cutler, Peter R. Schreiner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . Koninginin B ÏàËÆ¶È:75% Journal of Agricultural and Food Chemistry 1991 39 977-980 Koninginin B: a biologically active congener of koninginin A from Trichoderma koningii Horace G. Cutler, David S. Himmelsbach, Boris Yagen, Richard F. Arrendale, John M. Jacyno, Patsy D. Cole, Richard H. Cox Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . PiValoate C15H26O3 ÏàËÆ¶È:68.7% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . (4S,6R)-6-(tert-butyldimethylsilyloxy)tridec-1-yn-4-ol C19H38O2Si ÏàËÆ¶È:64.7% Tetrahedron 2012 68 3179-3186 Organocatalytic enantioselective synthesis of 1,3,5-polyols by means of iterative asymmetric epoxidation: their application to the total synthesis of polyrhacitide A Gullapalli Kumaraswamy, Akula Narayana Murthy, Kadivendi Sadaiah Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . (S)-methyl 2-(tert-butyldimethylsilyloxy)-2-((4S,5R)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl)acetate C21H42O5Si ÏàËÆ¶È:63.1% The Journal of Organic Chemistry 2011 76 2029-2039 Enantioselective Synthesis of Possible Diastereomers of Heptadeca-1-ene-4,6-diyne-3,8,9,10-tetrol; Putative Structure of a Conjugated Diyne Natural Product Isolated from Hydrocotyle leucocephala Kavirayani R. Prasad and Bandita Swain Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . compound 13 ÏàËÆ¶È:63.1% Tetrahedron 1997 53 15691-15700 The absolute stereostructures of the polyacetylenic constituents of Ginseng Radix Rubra Motomasa Kobayashi, Taifo Mahmud, Takashi Umezome, Weiqi Wang, Nobutoshi Murakami, Isao Kitagawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 7 C16H26O4 ÏàËÆ¶È:62.5% Journal of Natural Products 1993 Vol 56 1799 Antifungal Metabolites from Trichoderma harzianum Emilio L. Ghisalberti, Catherine Y. Rowland Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . (S)-1-[(4S,5R)-5-Ethynyl-2,2-dimethyl-1,3-dioxolan-4-yl]octan-1-ol C15H26O3 ÏàËÆ¶È:62.5% The Journal of Organic Chemistry 2011 76 2568-2576 Stereoselective Total Synthesis of (+)-Oploxyne A, (-)-Oploxyne B,and Their C-10 Epimers and Structure Revision of Natural Oploxyne B J. S. Yadav, Kumaraswamy Boyapelly, Sathish Reddy Alugubelli, Srihari Pabbaraja,Janakiram R Vangala, and Shasi V Kalivendi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 11-Hydroxy cubebol C15H26O2 ÏàËÆ¶È:62.5% Phytochemistry 1981 20 2383-2387 Labdane derivatives from hemizonia species Ferdinand Bohlmann, Jasmin Jakupovic, Maniruddin Ahmed, Michael Wallmeyer, Harold Robinsont, Robert M. King Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . koninginin E ÏàËÆ¶È:62.5% Bioscience, Biotechnology, and Biochemistry 1995 59 1747-1749 Koninginin E : Isolation of a Biologically Active Natural Product from Trichoderma koningii Stephen R. Parker, Horace G. Cutler, Peter R. Schreiner Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . compound 3a C12H20O3 ÏàËÆ¶È:62.5% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . Propionate C13H22O3 ÏàËÆ¶È:62.5% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . Butyrate C14H24O3 ÏàËÆ¶È:62.5% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . Valerate C15H26O3 ÏàËÆ¶È:62.5% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . Isobutyrate C14H24O3 ÏàËÆ¶È:62.5% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . tert-Butyl Acetate C16H28O3 ÏàËÆ¶È:62.5% Journal of Agricultural and Food Chemistry 2002 50 3522-3526 Antimicrobial and Bactericidal Activities of Esters of 2-endo-Hydroxy-1,8-cineole as New Aroma Chemicals Mitsuo Miyazawa and Yuya Hashimoto Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (R)-(2,2-Dimethyl-1,3-dioxolan-4-yl)methyl stearate C24H46O4 ÏàËÆ¶È:62.5% Organic & Biomolecular Chemistry 2012 10 1374-1380 Design and synthesis of fluorescence-labeled closo-dodecaborate lipid: its liposome formation and in vivo imaging targeting of tumors for boron neutron capture therapy Hiroyuki Nakamura, Noriko Ueda, Hyun Seung Ban, Manabu Ueno and Shoji Tachikawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . (aS,4R)-2,2-Dimethyl-a-tetradecyl-1,3-dioxolane-4-methanol ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2013 96 505-513 Stereoselective Total Synthesis of Passifloricin A Cheruku Ravindra Reddy, Boyapati Veeranjaneyulu, Siddavatam Nagendra and Biswanath Das Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 18-bromo-(9E,17E)-octadeca-9,17-diene-5,7-diynoic acid ÏàËÆ¶È:61.1% Journal of Natural Products 1992 Vol 55 1170 Brominated Polyacetylenic Acids from the Marine Sponge Xestospongia muta: Inhibitors of HIV Protease Ashok D. Patil, Wilhelmus C. Kokke, Sally Cochran, Terry A. Francis, Thaddeus Tomszek, John W. Westley Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . (S)-methyl 2-((tert-butyldimethylsilyl)oxy)-2-((4S,5R)-5-(hex-5-en-1-yl)-2,2-dimethyl-1,3-dioxolan-4-yl)acetate C20H38O5Si ÏàËÆ¶È:61.1% Tetrahedron 2013 69 6507-6511 Enantiospecific formal total synthesis of (+)-aspicilin Vasudeva Rao Gandi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . monocleolic acid C18H30O3 ÏàËÆ¶È:58.8% Phytochemistry 1988 27 2603-2608 Fatty acids and cyclic bis(bibenzyls) from the New Zealand liverwort Monoclea forsteri Masao Toyota,Fumihiro Nagashima,Yoshinori Asakawa Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . 15-Acetoxypentadecan-12-olide C17H30O4 ÏàËÆ¶È:58.8% Tetrahedron Letters 2002 43 1321-1324 A rearrangement of 1-hydroperoxy-2-oxabicycloalkanes into lactones of ¦Ø-acyloxy-(¦Ø-3)-hydroxyalkanoic acids related to the Criegee reaction Yuri N Ogibin, Alexandre O Terent'ev, Alexandre V Kutkin, Gennady I Nikishin Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 25 . compound 2j ÏàËÆ¶È:58.8% Tetrahedron Letters 2003 44 6703-6707 Versatile palladium(II)-catalyzed Negishi coupling reactions with functionalized conjugated alkenyl chlorides Jean-François Peyrat, Emmanuel Thomas, Nathalie L'Hermite, Mouâd Alami, Jean-Daniel Brion Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 26 . vernolicacid C18H32O3 ÏàËÆ¶È:58.8% Natural Product Research and Development 2000 12(2) 1-3 A NEW ALKALOID FROM THE SEEDS OF ALLIUM TUBEROSUM Sang Shengmin; Mao Shilong; Lao Aina; Chen Zhongliang Structure 13C NMR ̼Æ×Ä£Äâͼ |
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