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1 .     compound G.
C48H57NO7SSi     ÏàËÆ¶È:60.6%
Tetrahedron          2013          69          4120-4138
Novel method for construction of tetrahydro-1-benzazepine and tetrahydro-2-benzazepine based on 7-endo selective Friedel¨CCrafts cyclization of vinyloxirane
Megumi Mizukami, Koji Wada, Gen Sato, Yusuke Ishii, Norio Kawahara, Shinji Nagumo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (1S,4aS,8aR)-Methyl-5-{2-[2-(2-oxo-2-benzylaminoacetyl)furan-3-yl]ethyl}-1,4a,6-trimethyl-1,2,3,4,4a,7,8,8aoctahydronaphthalen- 1-carboxylate
C30H37NO5     ÏàËÆ¶È:56.6%
Chemistry of Natural Compounds          2010          46          233-241
Synthetic transformations of higher terpenoids. XXI.* Preparation of phlomisoic acid and its N-containing derivatives
M. E. Mironov, Yu. V. Kharitonov, E. E. Shul¡¯ts, M. M. Shakirov and I. Yu. Bagryanskaya, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     sarcotragins A
C31H43NO4     ÏàËÆ¶È:56.6%
Tetrahedron Letters          2001          42          3005-3007
Sarcotragins A and B, new sesterterpenoid alkaloids from the sponge Sarcotragus sp.
Jongheon Shin, Jung-Rae Rho, Youngwan Seo, Hyi-Seung Lee, Ki Woong Cho, Chung J. Sim
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     2-[N-(tolylsulfonyl)-N-[4-[(tert-butyldiphenylsilyl)oxy]butyl]amino]-4-[(tert-butyldiphenylsilyl)oxy]-1-iodo-butan-4-ol
C47H60INO4SSi2     ÏàËÆ¶È:56.6%
Journal of Medicinal Chemistry          1995          38          2714-2727
Synthesis and Biochemical Evaluation of Adenosylspermidine, a Nucleoside-Polyamine Adduct Inhibitor of Spermidine Synthase
John R. Lakanen, Anthony E. Pegg, James K. Coward
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     N-(tert-butyl)-9-{4-[4-(tert-butyldiphenylsilyloxy)-methyl]benzoylphenyl}-3,4-dihydro-2H,6H-pyrimido[1,2-c][1,3]benzothiazin-6-imine
C45H47N3O2SSi     ÏàËÆ¶È:56.6%
Bioorganic & Medicinal Chemistry          2013          21          2079-2087
Design and synthesis of biotin- or alkyne-conjugated photoaffinity probes for studying the target molecules of PD 404182
Tsukasa Mizuhara, Shinya Oishi, Hiroaki Ohno, Kazuya Shimura, Masao Matsuoka, Nobutaka Fujii
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     Mesylate
C28H36O4S     ÏàËÆ¶È:56.6%
Journal of the American Chemical Society          1998          120          12777-12782
A Direct and Efficient Stereocontrolled Synthetic Route to the Pseudopterosins, Potent Marine Antiinflammatory Agents
E. J. Corey and Scott E. Lazerwith
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     9-((1R,3R,4R,7S)-7-(Benzyloxy)-1-((tert-butyldiphenylsilyloxy) methyl)-2,5-dioxabicyclo[2.2.1]heptan-3-yl)-2,6-di(furan-2-yl)-9H-purine
C42H40N4O6Si     ÏàËÆ¶È:56.2%
Bioorganic & Medicinal Chemistry          2011          19          5648-5669
Synthesis and biological evaluation of 2', 4'- and 3', 4'-bridged nucleoside analogues
K.C. Nicolaou, Shelby P. Ellery, Fatima Rivas, Karen Saye, Eric Rogers, Tyler J. Workinger, Mark Schallenberger, Rommel Tawatao, Ana Montero, Ann Hessell, Floyd Romesberg, Dennis Carson, Dennis Burton
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     1-(4-chlorophenyl)-3,3-bis(4-methylphenyl)-1'-methyl-spiro-[azetidine-2,3'-indoline]-2',4-dione
C31H25N2O2Cl     ÏàËÆ¶È:53.3%
Journal of Heterocyclic Chemistry          2006          43          1665-1668
Reactions of ¦Á-diazoketones with indolinone imines: Synthesis of new 1,3,3-triaryl-1'-methylspiro[azetidine-2,3'-indoline]-2',4-diones
Girija S. Singh and Boycie J. Mmolotsi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     compound 26c
C31H29N3O6     ÏàËÆ¶È:53.3%
Heterocycles          2006          70          367-388
Cycloaddition Reactions of Amino-Acid Derived Cross-Conjugated Trienes: Stereoselective Synthesis of Novel Heterocyclic Scaffolds
Branko Mitasev, Bingli Yan, and Kay M. Brummond*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     Jolkinol B
C29H36O5     ÏàËÆ¶È:53.3%
Chinese Traditional and Herbal Drugs          2004          35          611-613
Diterpenoids from Euphorbia wallichii
WANG Huan; ZHANG Xiao-feng; MA Yun-bao; CAI Xiang-hai; WU Da-gang; LUO Xiao-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     3,8-Dimethyl-N,N,5-tri(propan-2-yl)benzoheptaleno[1',2':5,6]benzo[1,2-d]thiophen-10-amine 11,11-dioxide
C33H37NO2S     ÏàËÆ¶È:53.3%
Heterocycles          2011          82          1195-1202
Nucleophilic Reactions of 9-Isopropyl-2,4-dimethoxy-7,12-dimethyl-3-(phenylsulfonyl)benzo[a]heptalene with Lithium Dialkylamides
Samir El Rayes, Anthony Linden, Khaled Abou-Hadeed, and Hans-J¨¹rgen Hansen*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     syn-(¡À)-4-(2'-Methoxybiphenyl-4-yl)-3,6-dimethyl-1-(2-methylphenyl)-4,8-dihydro-1H-pyrazole[3,4-e][1,4]thiazepin-7-one
C28H27N3OS     ÏàËÆ¶È:53.3%
Bioorganic & Medicinal Chemistry          2012          20          3429-3445
Pyrazole[3,4-e][1,4]thiazepin-7-one derivatives as a novel class of Farnesoid X Receptor (FXR) agonists
Maura Marinozzi, Andrea Carotti, Emanuele Sansone, Antonio Macchiarulo, Emiliano Rosatelli, Roccaldo Sardella, Benedetto Natalini, Giovanni Rizzo, Luciano Adorini, Daniela Passeri, Francesca De Franco, Mark Pruzanski, Roberto Pellicciari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     (4-Benzyloxy-3-isopropylphenyl)-(7-dibenzylamino-5-methylindan-4-yl)methanol
C41H43NO2     ÏàËÆ¶È:53.3%
Bioorganic & Medicinal Chemistry          2012          20          3622-3634
Discovery of novel indane derivatives as liver-selective thyroid hormone receptor ¦Â (TR¦Â) agonists for the treatment of dyslipidemia
Hiroaki Shiohara, Tetsuya Nakamura, Norihiko Kikuchi, Tomonaga Ozawa, Ryuichi Nagano, Akane Matsuzawa, Hideki Ohnota, Takahide Miyamoto, Kazuo Ichikawa, Kiyoshi Hashizume
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     [(2S,3S)-3-{(E,3R,4R,5R,6R)-5-[(tert-Butyldimethylsilyl)oxy]-7-[(tert-butyldiphenylsilyl)oxy]-3-methoxy-1,4,6-trimethyl-1-heptenyl}-oxiran-2-yl]methyl 4-Methyl-1-benzenesulfonate
C43H64O7Si2S     ÏàËÆ¶È:53.3%
European Journal of Organic Chemistry          2012                   2062-2071
Towards the Synthesis of (¨C)-Callipeltoside A: Stereoselective Synthesis of the C1¨CC14 Macrolactone Core
Jhillu S. Yadav, Animesh Haldar and Tapas Maity
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     (2R,4E,6R,7R,8R,9R)-8-[(tert-Butyldimethylsilyl)oxy]-10-[(tert-butyldiphenylsilyl)oxy]-2-hydroxy-6-methoxy-4,7,9-trimethyl-4-decenyl-4-Methyl-1-benzenesulfonate
C43H66O7Si2S     ÏàËÆ¶È:53.3%
European Journal of Organic Chemistry          2012                   2062-2071
Towards the Synthesis of (¨C)-Callipeltoside A: Stereoselective Synthesis of the C1¨CC14 Macrolactone Core
Jhillu S. Yadav, Animesh Haldar and Tapas Maity
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     Z,E,Z-cupaniopsin C 22-hydroxy derivative
C30H44O4     ÏàËÆ¶È:53.3%
Tetrahedron          2005          61          845-851
New biologically active linear triterpenes from the bark of three new-caledonian Cupaniopsis species
H. Bousserouel, M. Litaudon, B. Morleo, M.-T. Martin, O. Thoison, O. Nosjean, J.A. Boutin, P. Renard, T. S¨¦venet
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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