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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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

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