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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×Ä£Äâͼ

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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   Ì¼Æ×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   Ì¼Æ×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   Ì¼Æ×Ä£Äâͼ
2Â¥2013-09-30 07:58:01
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