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213.2,  82.5,  76.3,  54.3,  54.1,  46.7, 38.2,  31.5,  29.4,  29.4, 28.1, 24.3, 24.3, 20.1
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1 .     alkaloid nitramine
    ÏàËÆ¶È:58.3%
Chemistry of Natural Compounds          1981          17          458-463
NMR INVESTIGATION OF ALKALOIDS.II. DETERMINATION OF THE CONFIGURATIONS OF THE C17 and C2 ASYMMETRIC CENTERS IN INDOLINE ALKALOIDS OF THE AJMALINE TYPE THE DOUBLE PROTON RESONANCE METHOD
M. R. Yagudaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     1-spiro[5.5]undec-2-ylethanone
    ÏàËÆ¶È:58.3%
Organic letters          2000          2          3769-3772
Annulation of the Cyclohexane Ring by Tandem Free Radical Alkylation of a Nonactivated ¦Ä-Carbon Atom−Intramolecular Carbanion Cycloalkylation
Goran Petrovic and Zivorad Cekovic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     4-[(6-methylheptan-2-yl)amino]-4-oxobutanoic acid
C12H23NO3     ÏàËÆ¶È:58.3%
Journal of Heterocyclic Chemistry          2010          47          188-193
The synthesis and characterization of solvatochromic maleimide-fused N-allyl- and N-alkyl-substituted 1,4-dithiines and Diels¨CAlder reactions with anthracene
Şirin G¨¹lten
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     enniatin C
C36H63N3O9     ÏàËÆ¶È:58.3%
Tetrahedron          2003          59          1015-1020
Unusual enniatins produced by the insect pathogenic fungus Verticillium hemipterigenum: isolation and studies on precursor-directed biosynthesis
Chongdee Nilanonta, Masahiko Isaka, Rachada Chanphen, Nuntawan Thong-orn, Morakot Tanticharoen, Yodhathai Thebtaranonth
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     (1R,2S,5R) 2-ethoxycarbonyl-1-hydroxy-5-methylbicyclo[4.3.0]-nonane-6-one
    ÏàËÆ¶È:58.3%
Tetrahedron          2012          68          3457-3467
An easy route toward enantio-enriched polycyclic derivatives via an asymmetric domino conjugate reduction¨Caldol cyclization catalyzed by a chiral Cu(I) complex
Julia Deschamp, Thomas Hermant, Olivier Riant
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     compound 6A
    ÏàËÆ¶È:58.3%
Organic Magnetic Resonance          1983          21          217-220
Carbon-13 NMR spectra of several dicyclopentadiene derivatives
Brian A. Dawson and J. B. Stothers
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
7 .     trans-2-PinanoI
    ÏàËÆ¶È:58.3%
Organic Magnetic Resonance          1975          7          125-127
Conformational studies of monoterpenes. II¨Cconformational studies of bicyclo[3.1.1]heptane derivatives by 13C NMR
Collette M. Holden and David Whittaker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
8 .     Allo-aromadendrane-10¦Â,14-diol
    ÏàËÆ¶È:57.1%
Archives of Pharmacal Research          2008          31          21-27
A new sesquiterpene and other terpenoid constituents of Chisocheton penduliflorus
Jarinporn Phongmaykin, Takuya Kumamoto, Tsutomu Ishikawa, Rutt Suttisri and Ekarin Saifah
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
9 .     (-)-7-oxo-2,6,6-trimethyltricyclo[6,2,1,0(1,5)]undecane
C14H22O     ÏàËÆ¶È:57.1%
Tetrahedron          1990          46          761-774
Stereocontrolled synthesis of (-)-prezizanol,(-)-prezizaene, their epimers and (-)-allokhusiol
Kazutoshi Sakurai, Takeshi Kitahara, Kenji Mori
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
10 .     MKN-003A
C13H20O3     ÏàËÆ¶È:53.8%
Journal of Natural Products          2001          64          664-667
New Lactone-Containing Metabolites from a Marine-Derived Bacterium of the Genus Streptomyces
Ki Woong Cho, Hyi-Seung Lee, Jung-Rae Rho, Tae Sik Kim, Sang Jun Mo, and Jongheon Shin
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
11 .     4-hydroxy-10-methyl-11-oxo-dodec-2-en-1,4-olide
C13H20O3     ÏàËÆ¶È:53.8%
Journal of Natural Products          2000          63          1570-1572
New Butenolides from Two Marine Streptomycetes
Venugopal J. R. V. Mukku, Michael Speitling,Hartmut Laatsch, and Elisabeth Helmke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
12 .     3,5,5-trimethyl-3-butylcyclohexanone
    ÏàËÆ¶È:53.8%
Tetrahedron Letters          2001          42          2415-2417
Preparation and reactivity of cyanocuprates containing alkylseleno and alkyltelluro groups as non-transferable ligands
Fabiano K Zinn, Eduardo C Ramos, João V Comasseto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
13 .     (S)-(-)-2-(2-Diazoacetyl)-1-trifluoroacetylpyrrolidine
C8H8F3N3O2     ÏàËÆ¶È:53.8%
Journal of the Chemical Society, Perkin Transactions 1          2001                   3325-3337
Rearrangement of ammonium ylides produced by intramolecular reaction of catalytically generated metal carbenoids. Part 2. Stereoselective synthesis of bicyclic amines
J. Stephen Clark, Paul B. Hodgson, Michael D. Goldsmith, Alexander J. Blake, Paul A. Cooke and Leslie J. Street
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
14 .     compound 9a
C13H18O2     ÏàËÆ¶È:53.8%
Heterocycles          2001          54          765-776
Intramolecular Photocycloaddition of 2-Cycloalkenyl-1,3-dioxin-4-one. Stereoselective Synthesis of cis-Eudesmane-4,11-diols
Toshihide Hatsui,* Ka Li, Akira Mori,* and Hitoshi Takeshita
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
15 .     3R,9R-oxido-5-megastigmene
C13H22O     ÏàËÆ¶È:53.8%
Molecules          2012          17          3539-3546
A New Norisoprenoid and Other Compounds from Fuzhuan Brick Tea
Zhen-Mei Luo, Tie-Jun Ling, Li-Xiang Li, Zheng-Zhu Zhang, Hong-Tao Zhu, Ying-Jun Zhang and Xiao-Chun Wan
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
16 .     compound 2d
    ÏàËÆ¶È:53.8%
Organic Magnetic Resonance          1982          19          91-94
Carbon-13 NMR investigation of some pharmacologically important cyclic n-alkynylamines
Jasim M. A. Al-Rawi, George Q. Behnam, Salman R. Salman, Zuhair Muhi-Eldeen and Fuad H. Al-Jawad
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
17 .     (R)-2-[(1S,2R)-3,3-Dimethyl-2-(3-oxo-1-butenyl)cyclobutyl]-2-hydroxypropanal
C13H20O3     ÏàËÆ¶È:53.8%
Tetrahedron          2012          68          4581-4587
Synthesis of rumphellaone A via epoxy nitrile cyclization
Takafumi Hirokawa, Shigefumi Kuwahara
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
18 .     compound 6
    ÏàËÆ¶È:53.3%
Journal of Natural Products          1994          Vol 57          369
Conformational Analysis of Moreliene Derivatives
Carlos M. Cerda-Garc¨ªa-Rojas, Rosa E. del R¨ªo, Pedro Joseph-Nathan, Luisa U. Rom¨¢n, Juan D. Hern¨¢ndez
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
19 .     4,11-Epoxy-hydroxyamoyphane
C15H26O2     ÏàËÆ¶È:53.3%
Phytochemistry          1994          35          425-433
The sesquiterpenes of Fabiana imbricata
Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
20 .     compound 14
    ÏàËÆ¶È:53.3%
Phytochemistry          1989          28          2717-2721
Sesquiterpenoids and phenolics of Pulicaria paludosa
Arturo San Feliciano,Manuel Medarde,Marina Gordaliza,Esther Del Olmo,Jos¨¦ M. Miguel del Corral
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
21 .     (+)-10¦Â,14-dihydroxy-allo-aromadendrane
    ÏàËÆ¶È:53.3%
Magnetic Resonance in Chemistry          2003          41          1034-1037
Complete NMR assignment of (+)-10¦Â, 14-dihydroxy-allo-aromadendrane
Lucin¨¦ia Vizzotto, Rozanna Marques Muzzi and D¨ºnis Pires de Lima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
22 .     (+)-10¦Â,14-dihydroxy-allo-aromadendrane
    ÏàËÆ¶È:53.3%
Magnetic Resonance in Chemistry          2003          41          1034-1037
Complete NMR assignment of (+)-10¦Â, 14-dihydroxy-allo-aromadendrane
Lucin¨¦ia Vizzotto, Rozanna Marques Muzzi and D¨ºnis Pires de Lima
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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