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142.5, 131.3, 61.5, 56.6, 40.6, 33.8, 31.9, 31.4, 29.1, 29.0, 28.9, 25.7, 24.6, 23.7, 22.4, 13.9.
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1 .     bgugaine
C19H39N     ÏàËÆ¶È:75%
Natural Product Research          1993          2          237-242
Antibiotic and Antifungal Pyrrolidine Alkaloids, from Arisarum vulgare
Ahmed Melhaoui; Monique Mallea; Akino Jossang; Bernard Bodo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     2R-bgugaine/2S-bgugaine
    ÏàËÆ¶È:75%
Natural Product Research          2009          23          659-664
Anti-cancer effect of two alkaloids: 2R and 2S-bgugaine on mastocytoma P815 and carcinoma Hep
Malika Benamar; Ahmed Melhaoui; Abdelmajid Zyad; Ibrahim Bouabdallah; Mohammed Aziz
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     (R)-bgugaine
C19H39N     ÏàËÆ¶È:75%
Journal of Chemical Research          2008          32          121-122
A concise synthesis of (R)-Bgugaine, a pyrrolidine alkaloid from Arisarum vulgare
Majik, Mahesh S.; Parameswaran, P.S.; Tilve, Santosh G.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     (S)-1-tert-Butyl-2-(hexylcarbamoyl)pyrrolidine-1-carboxylate
C16H30N2O3     ÏàËÆ¶È:75%
Tetrahedron          2012          68          5415-5421
The phosphate¨Ccarboxylate mixed-anhydride method: a mild, efficient process for ester and amide bond construction
James McNulty, Ramesh Vemula, Venkatesan Krishnamoorthy, Al Robertson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     methyl(10E)-12-octadec-10-enoate
    ÏàËÆ¶È:70.5%
Russian Journal of Organic Chemistry          2001          37          781-783
Isomerization of Methyl (9Z)-12-Oxooctadec-9-enoate
A. M. Davletbakova, N. Z. Baibulatova, V. A. Dokichev, S. G. Yunusova and M. S. Yunusov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     liguloxide
    ÏàËÆ¶È:68.7%
Phytochemistry          1991          30          3669-3677
Friedolabdanes and other constituents from chileanHaplopappus species
C. Zdero, F. Bohlmann, H.M. Niemeyer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     Compound 9
    ÏàËÆ¶È:68.7%
Bioorganic & Medicinal Chemistry Letters          2003          13          1977-1980
Hemisynthesis and preliminary evaluation of novel endocannabinoid analogues
Siham El Fangour, Laurence Balas, Jean-Claude Rossi, Andrey Fedenyuk, Natalia Gretskaya, Mikhail Bobrov, Vladimir Bezuglov, Cecilia J. Hillard, Thierry Durand
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     1,12-bis(3'-pentylpyridinium)dodecane dichloride
C32H54Cl2N2     ÏàËÆ¶È:68.7%
Bioorganic & Medicinal Chemistry          2009          17          6329-6339
Synthesis, antifungal, haemolytic and cytotoxic activities of a series of bis(alkylpyridinium)alkanes
Daniel Obando, Namfon Pantarat, Rosemary Handke, Yasuko Koda, Fred Widmer, Julianne T. Djordjevic, David H. Ellis, Tania C. Sorrell, Katrina A. Jolliffe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     n-hexyl laurate
    ÏàËÆ¶È:68.7%
Journal of Chemical Ecology          2012          38          23-28
n-Hexyl Laurate and Fourteen Related Fatty Acid Esters:New Secretory Compounds from the Julid Millipede,Anaulaciulus sp.
Nobuhiro Shimizu & Yasumasa Kuwahara & Ryota Yakumaru & Tsutomu Tanabe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     (¡À) 9'-epi-3¦Â,3'¦Â-dimethylxestospongin C
C30H54N2O2     ÏàËÆ¶È:68.7%
Planta Medica          2011          77          179-181
9'-Epi-3¦Â,3'¦Â¨Cdimethylxestospongin C, a New Macrocyclic Diamine Alkaloid from the Hainan Sponge Neopetrosia exigua
Yan Li, Song Qin, Yue-Wei Guo, Yu-Cheng Gu, Rob W. M. van Soest
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     (S)-1-tert-Butyl-2-(hexylcarbamoyl)pyrrolidine-1-carboxylate
C16H30N2O3     ÏàËÆ¶È:68.7%
Tetrahedron          2012          68          5415-5421
The phosphate¨Ccarboxylate mixed-anhydride method: a mild, efficient process for ester and amide bond construction
James McNulty, Ramesh Vemula, Venkatesan Krishnamoorthy, Al Robertson
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     (e)-8-oxo-9-oactadecenoic acid
C18H32O3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2002          65          1712-1714
Aldehyde Dehydrogenase Inhibitors from the Mushroom Clitocybe clavipes
Hirokazu Kawagishi, Toshiyuki Miyazawa,Hiroko Kume,Yasushi Arimoto, and Takahiro Inakuma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     compound 5
18H32O3     ÏàËÆ¶È:66.6%
Journal of Natural Products          2002          65          1712-1714
Aldehyde Dehydrogenase Inhibitors from the Mushroom Clitocybe clavipes
Hirokazu Kawagishi, Toshiyuki Miyazawa,Hiroko Kume,Yasushi Arimoto, and Takahiro Inakuma
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     (E)-11-oxo-octadeca-12-enoic acid
C19H34O3     ÏàËÆ¶È:66.6%
Zeitschrift f¨¹r Naturforschung B          2009          64b          1199-1207
Three New Unsaturated Fatty Acids from the Marine Green Alga Ulva fasciata Delile
Ghada S. E. Abou-ElWafa, Mohamed Shaaban, Khaled A. Shaaban,Mohamed E. E. El-Naggar, and Hartmut Laatsch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     Compound 4b
C19H37NO     ÏàËÆ¶È:66.6%
Bioorganic & Medicinal Chemistry Letters          1994          4          1317-1318
Inhibition of oxidosqualene cyclase by substituted quinolizidines
Angela L. Marquart, Gerald L. Schatzman, Norton P. Peet, William R. Moore, Edward W. Huber, Steven L. Gallion, Michael R. Angelastro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (E)-Octadec-9-en-11-olide
C18H32O2     ÏàËÆ¶È:66.6%
Organic & Biomolecular Chemistry          2007          5          3434-3441
Macrolides from the scent glands of the tropical butterflies Heliconius cydno and Heliconius pachinus
Stefan Schulz, Selma Yildizhan, Katja Stritzke, Catalina Estrada and Lawrence E. Gilbert
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     methyl (9Z,12R)-12-methoxy-9-octadecenoate
    ÏàËÆ¶È:66.6%
Russian Journal of Organic Chemistry          2001          37          608-611
Catalytic Cyclopropanation of Ricinolic Acid Derivatives with Diazomethane
A. M. Davletbakova, I. O. Maidanova, N. Z. Baibulatova, V. A. Dokichev and Yu. V. Tomilov, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     compound 1a/1b
C38H78NO5     ÏàËÆ¶È:65%
Journal of Natural Products          2001          64          1210-1215
Sex Pheromones of the Hair Crab Erimacrus isenbeckii. II. Synthesis of Ceramides
Naoki Asai, Nobuhiro Fusetani, and Shigeki Matsunaga
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     (S)-13-hydroxy-9Z,11E-octadecadienoic acid
C18H32O3     ÏàËÆ¶È:64.7%
China Journal of Chinese Materia Medica          2004          29          1108-1109
Èý·Öµ¤»¯Ñ§³É·ÖµÄÑо¿
»ÆÑ§Ê¯, Û¬ áÔ, ·¶Àö»ª, â×ʯɽ , ÁºÏþÌì
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     decyl 8-oxoheptadecanoate
    ÏàËÆ¶È:64.7%
Indian Journal of Chemistry          2010          49B          1648-1652
Total synthesis of three natural products: Decyl 8-hydroxyheptadecanoate,undecyl hexadecanoate and 2,3-dihydroxypropyl hexadecanoate
Ashima Singh,M L Sharma & Jasvinder Singh*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-04-26 15:40:08
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