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304846814

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¦Ä 22.31, 24.30, 27.65, 30.78, 32.59, 48.52, 52.22, 66.09, 66.38, 69.83, 73.42, 74.50, 76.34, 86.11, 88.30, 102.04, 115.41, 125.95 , 127.38£¬127.67, 128.10,,129.60£¬129.94, 137.71, 156.19

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[ Last edited by 304846814 on 2012-9-12 at 10:50 ]
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1 .     Methyl (4S,5R)-5-[(E,R)-1-Benzyloxy-5-bromopent-3-en-1-yl]-4-(4-methoxybenzyloxymethyl)-2-oxooxazolidine-4-carboxylate
C26H31BrNO7     ÏàËÆ¶È:62.5%
Bulletin of the Chemical Society of Japan          2002          75          1927-1947
Total Synthesis of (+)-Myriocin and (−-Sphingofungin E from Aldohexoses Using Overman Rearrangement as the Key Reaction
Takeshi Oishi, Koji Ando, Kenjin Inomiya, Hideyuki Sato, Masatoshi Iida, Noritaka Chida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (S)-1,5-[2-(diphenylphosphanyl)ferrocene-1,1'-diyl]pent-1-ene
C27H25PFe     ÏàËÆ¶È:62.5%
European Journal of Organic Chemistry          2011                   6110-6116
[5]Ferrocenophanene¨CPhosphane Ligands for Enantioselective Rh-Catalyzed Conjugate Additions
Jana Csizmadiov¨¢, M¨¢ria Mečiarov¨¢, Erik Rakovský, Branislav Horv¨¢th and Radovan Šebesta
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     1,4-Anhydro-2,3,5,6-di-O-isopropylidene-1-[(S)-[(2'S,3'S)-2',4'-benzylidenedioxy-3'-(sulfooxy)butyl]sulfonio]-D-allitol inner salt
C23H32O10S2     ÏàËÆ¶È:58.3%
Canadian Journal of Chemistry          2006          84          1351-1362
Design and synthesis of selenonium and sulfonium ions related to the naturally occurring glucosidase inhibitor salacinol1
Hui Liu and B. Mario Pinto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     1,4-Anhydro-2,3,5,6-di-O-isopropylidene-1-[(S)-[(2'S,3'S)-2',4'-benzylidenedioxy-3'-(sulfooxy)butyl]sulfonio]-L-allitol inner salt
C23H33O10S2     ÏàËÆ¶È:58.3%
Canadian Journal of Chemistry          2006          84          1351-1362
Design and synthesis of selenonium and sulfonium ions related to the naturally occurring glucosidase inhibitor salacinol1
Hui Liu and B. Mario Pinto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     2-arachidonyl-cis-1,3-O-benzylideneglycerol
    ÏàËÆ¶È:58.3%
Tetrahedron Letters          2000          41          3589-3592
Facile synthesis and stabilization of 2-arachidonylglycerol via its 1,3-phenylboronate ester
Herbert H. Seltzman, Denise N. Fleming, Gregory D. Hawkins, F. Ivy Carroll
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     compound 7 derivative
C29H44O2S     ÏàËÆ¶È:58.3%
The Journal of Organic Chemistry          2009          74          5267-5275
Structural and Synthetic Investigations of Tanikolide Dimer, a SIRT2 Selective Inhibitor, and Tanikolide seco-Acid from the Madagascar Marine Cyanobacterium Lyngbya majuscula
Marcelino Gutierrez, Eric H. Andrianasolo, Won Kyo Shin, Douglas E. Goeger, Alexandre Yokochi, Jorg Schemies, Manfred Jung, Dennis France, Susan Cornell-Kennon, Eun Lee and William H. Gerwick
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     compound 12
C24H30O6     ÏàËÆ¶È:58.3%
Tetrahedron          2012          68          2245-2260
A convergent synthesis of the right-hand fragment of ciguatoxin CTX3C
Hiroyoshi Takamura, Takashi Abe, Naoki Nishiuma, Rie Fujiwara, Takahiko Tsukeshiba, Isao Kadota
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     (2S,4S)-4-[(benzyloxy)methyl]-1-(1,3-dioxan-2-yl)-2-methylpentadecan-4-ol
C28H48O4     ÏàËÆ¶È:58.3%
European Journal of Organic Chemistry          2011                   7097-7106
Asymmetric Synthesis of (+)-Tanikolide and the ¦Â-Methyl-Substituted Analogues of (+)-Tanikolide and (¨C)-Malyngolide
Robert Doran, Lesley Duggan, Surrendra Singh, Colm D. Duffy and Patrick J. Guiry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     (2R,4S)-4-[(benzyloxy)methyl]-1-(1,3-dioxan-2-yl)-2-methylpentadecan-4-ol
C28H48O4     ÏàËÆ¶È:56%
European Journal of Organic Chemistry          2011                   7097-7106
Asymmetric Synthesis of (+)-Tanikolide and the ¦Â-Methyl-Substituted Analogues of (+)-Tanikolide and (¨C)-Malyngolide
Robert Doran, Lesley Duggan, Surrendra Singh, Colm D. Duffy and Patrick J. Guiry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     sartone B
    ÏàËÆ¶È:54.1%
Journal of Natural Products          1999          62          1046-1049
New Cembranes from the Soft Coral Sarcophyton Species
Tetsuo Iwagawa, Ryozo Nakashima, Keita Takayama, Hiroaki Okamura, Munehiro Nakatani, Matsumi Doe, and Kozo Shibata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     maculalactone H
C34H30O6     ÏàËÆ¶È:54.1%
Journal of Natural Products          1998          61          29-33
Tribenzylbutyrolactones and Dibenzyldiphenyl-4, 5, 6, 7-tetrahydrobenzofuranones from Kyrtuthrix maculans
Sung-Chi Lee and Geoffrey D. Brown
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     16-Hydroxymethyl-3-benzyloxyestra-1,3,5(10)-trien-17-ol isomer 5a
C26H32O3     ÏàËÆ¶È:54.1%
Steroids          2002          67          371-377
Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers
P¨¢l Tapolcs¨¢nyi, J¨¢nos Wölfling, George Falkay, Árp¨¢d M¨¢rki, Ren¨¢ta Minorics, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     16-Hydroxymethyl-3-benzyloxyestra-1,3,5(10)-trien-17-ol isomer 5a
C26H32O3     ÏàËÆ¶È:54.1%
Steroids          2002          67          671-678
Synthesis and receptor-binding examination of 16-hydroxymethyl-3,17-estradiol stereoisomers
P¨¢l Tapolcs¨¢nyi, J¨¢nos Wölfling, George Falkay, Árp¨¢d M¨¢rki, Ren¨¢ta Minorics, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     1,4-Anhydro-2,3,5,6-di-O-isopropylidene-1-[(S)-[(2'S,3'S)-2',4-benzylidenedioxy-3'-(sulfooxy)butyl]selenonio]-L-allitol inner salt
C23H32O10SSe     ÏàËÆ¶È:54.1%
Canadian Journal of Chemistry          2006          84          1351-1362
Design and synthesis of selenonium and sulfonium ions related to the naturally occurring glucosidase inhibitor salacinol1
Hui Liu and B. Mario Pinto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

--------------------------------------------------------------------------------

15 .     compound 11
    ÏàËÆ¶È:54.1%
Tetrahedron Letters          2000          41          4751-4755
Solid-phase synthesis of hydroxy-acids leading to macrolactones
Ren¨¦ Gagnon, Yves L. Dory, Pierre Deslongchamps
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     oxazolidone
    ÏàËÆ¶È:54.1%
Tetrahedron Letters          2000          41          6429-6433
Novel stereoselective construction of a quaternary carbon: application to synthesis of the cyclopentenedione moiety of madindolines
Seijiro Hosokawa, Kazuhiko Sekiguchi, Manabu Enemoto, Susumu Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     5,6-di-O-benzyl-3-O-(diisopropylphosphonomethyl)-1-(uracil-1-yl)-¦Â-D-galactofuranose
C31H41N2O10P     ÏàËÆ¶È:54.1%
Heterocycles          2010          82          663-687
Synthesis and Anti-HIV Activity of New 3'-O-Phosphonomethyl Nucleosides
Michal Cesnek and Piet Herdewijn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     Compound 19
C21H37O5     ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry Letters          2004          14          4987-4990
Asymmetric synthesis of the stereoisomers of 11,12,15(S)-trihydroxyeicosa-5(Z),8(Z),13(E)-trienoic acid, a potent endothelium-derived vasodilator
J.R. Falck, Deb Barma, Suchismita Mohapatra, A. Bandyopadhyay, Komandla Malla Reddy, Jianjun Qi, William Campbell
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     KYS05044
C28H33N4O2     ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry Letters          2005          15          283-286
Synthesis and biological activity of 3,4-dihydroquinazolines for selective T-type Ca2+ channel blockers
Hyewhon Rhim, Yong Sup Lee, Seong Jun Park, Bong Young Chung, Jae Yeol Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     compound 24
C22H26O5S     ÏàËÆ¶È:54.1%
Tetrahedron Letters          2003          44          7837-7840
Cu(OTf)2-catalyzed Et3SiH-reductive etherification of various carbonyl compounds with trimethylsilyl ethers
Wei-Chieh Yang, Xin-An Lu, Suvarn S Kulkarni, Shang-Cheng Hung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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21 .     soyacerebroside I
    ÏàËÆ¶È:54.1%
Chinese Pharmaceutical Journal          2008          43          971-973
Studies on Chemical Constituents of Acetyl Acetate Extracted Fraction from Veratrum dahuricum
NIE Li-yue TANG Jian~LI Hui-liang JIN Hui-zi ZHANG Wei-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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22 .     4-Pentenyl 3-O-benzyl-4,6-O-(4-methoxybenzylidene)-¦Á-D-mannopyranoside
C26H32O7     ÏàËÆ¶È:54.1%
Bioorganic & Medicinal Chemistry          1996          4          2011-2022
New synthetic trisaccharide inhibitors for N-acetylglucosaminyltransferase-V
Pu-Ping Lu, Ole Hindsgaul, Catharine A. Compston, Monica M. Palcic
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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23 .     sartone B
C20H30O     ÏàËÆ¶È:54.1%
Bulletin of the Chemical Society of Japan          1996          69          3543-3549
Ichthyotoxic Cembranoids from the Soft Coral, Sarcophyton sp.
Tetsuo Iwagawa, Shun Nakamura, Hiroaki Okamura, Munehiro Nakatani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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24 .     Methyl (4S,5R)-5-[(E,R)-1-Benzyloxy-5-hydroxypent-3-en-1-yl]-4-(4-methoxybenzyloxymethyl)-2-oxooxazolidine-4-carboxylate
C26H31NO8     ÏàËÆ¶È:54.1%
Bulletin of the Chemical Society of Japan          2002          75          1927-1947
Total Synthesis of (+)-Myriocin and (−-Sphingofungin E from Aldohexoses Using Overman Rearrangement as the Key Reaction
Takeshi Oishi, Koji Ando, Kenjin Inomiya, Hideyuki Sato, Masatoshi Iida, Noritaka Chida
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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25 .     compound 19
C22H28O2Se     ÏàËÆ¶È:54.1%
Heterocycles          2002          57          293-305
Stereoselective Synthesis of Substituted Tetrahydropyran Rings via 6-exo and 6-endo Selenoetherification
Carmela Aprile, Michelangelo Gruttadauria,* Paolo Lo Meo, Serena Riela, and Renato Noto
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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26 .     (6S,7E,9R)-6,9-dihydroxy-4,7-megastigmadien-3-one 9-O-[¦Â-D-xylopyranosyl-(1''¡ú6')-¦Â-D-glucopyranoside]
    ÏàËÆ¶È:54.1%
Food Chemistry          2011          129          933-939
Terpenoids and hexenes from the leaves of Crataegus pinnatifida
Shao-Jiang Song, Ling-Zhi Li, Pin-Yi Gao, Ying Peng, Jing-Yu Yang, Chun-Fu Wu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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27 .     (R)-4-(benzyloxymethyl)-1-(1,3-dioxan-2-yl)pentadecan-4-ol
    ÏàËÆ¶È:54.1%
European Journal of Organic Chemistry          2011                   7097-7106
Asymmetric Synthesis of (+)-Tanikolide and the ¦Â-Methyl-Substituted Analogues of (+)-Tanikolide and (¨C)-Malyngolide
Robert Doran, Lesley Duggan, Surrendra Singh, Colm D. Duffy and Patrick J. Guiry
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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28 .     (1S,5S,6R,7S,8R,8aR)-6,7-bis(benzyloxy)-5,8-dihydroxy-5-propyl-1,2,3,5,6,7,8,8a-octahydronaphthalene-1-carbaldehyde
C28H34O5     ÏàËÆ¶È:54.1%
European Journal of Organic Chemistry          2011                   6281-6287
Synthesis of an A¡äB¡ä Precursor to Angelmicin B: Product Diversification in the Su¨¢rez Lactol Fragmentation
Jialiang Li, Louis Todaro and David R. Mootoo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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29 .     compound 52
C31H35N3O7     ÏàËÆ¶È:54.1%
European Journal of Organic Chemistry          2011                   1575-1586
Studies on Tetrahydrofuran-Based Highly O-Functionalized Alkynes: Applications to Synthesis of Tetrahydrofuranyl-Polyynes and C-Nucleoside Analogues
P. Venkat Reddy, Vikas Bajpai, Brijesh Kumar and Arun K. Shaw
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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30 .     Benzyl {(S)-6-Bromo-2-[(R)-4-(1-methylethyl)-2-oxo-5,5-diphenyloxazolidine-3-carbonyl]hexyl}-carbamate
C33H37BrN2O5     ÏàËÆ¶È:53.8%
Helvetica Chimica Acta          2010          93          314-323
Benzyl N-[(Benzyloxy)methyl]carbamate: An Improved Aminomethylation Electrophile for the Synthesis of (Benzyloxy)carbonyl (Cbz)-Protected Chiral ¦Â2-Amino Acids
Cara E. Brocklehurst, Markus Furegati, J. Constanze D. M¨¹ller-Hartwieg, Flavio Ossola and Luigi La Vecchia
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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31 .     Boc-L-MeLeu-D-morphPhLac-Obn
C32H44N2O7     ÏàËÆ¶È:53.8%
European Journal of Organic Chemistry          2012                   1546-1553
Segment Solid-Phase Total Synthesis of the Anthelmintic Cyclooctadepsipeptides PF1022A and Emodepside
J¨¹rgen Scherkenbeck, Sebastian L¨¹ttenberg, Monika Ludwig, Karin Br¨¹cher and Andreas Kotthaus
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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32 .     deacetylcytochalasin H
    ÏàËÆ¶È:53.8%
Journal of Agricultural and Food Chemistry          1983          31          405-408
Proton and carbon-13 nuclear magnetic resonance studies of the conformation of cytochalasin H derivatives and plant growth regulating effects of cytochalasins
Richard H. Cox, Philip Morris, Horace G. Cutler, Ralph E. Hurd, Richard J. Cole
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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33 .     4-(2-Benzyloxyethyl)phenyl 4,6-O-benzylidene-3-O-[4-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyl)benzyl]-¦Â-Dglucopyranoside
C46H41F17O7     ÏàËÆ¶È:53.5%
Tetrahedron          2011          67          8276-8292
Total synthesis of cucurbitoside-like phenolic glycosides by double fluorous and acyl mixture synthesis
Masaru Kojima, Yutaka Nakamura, Kazuki Komori, Shoji Akai , Ken-ichi Sato , Seiji Takeuchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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34 .     16¦Â-Acetoxymethyl-3-benzyloxy-17-methyl-18-nor-estra-1,3,5(10),13(17)-tetraene
C28H32O3     ÏàËÆ¶È:52%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
Ágota Sz¨¢jli, J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, Ren¨¢ta Minorics, Árp¨¢d M¨¢rki, George Falkay, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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35 .     3-benzyloxy-16¦Â-hydroxymethylestra-1,3,5(10),13(17)-tetraene
C26H30O2     ÏàËÆ¶È:52%
Steroids          2006          71          141-153
Neighboring group participation: Part 16. Stereoselective synthesis and receptor-binding examination of the four stereoisomers of 16-bromomethyl-3,17-estradiols
Ágota Sz¨¢jli, J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, Ren¨¢ta Minorics, Árp¨¢d M¨¢rki, George Falkay, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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36 .     Pent-4-enyl 3-O-benzyl-4,6-benzylidene-2-deoxy-2-tetrachiorophthalimido-¦Â-D-glucopyranoside
C33H29NO7Cl4     ÏàËÆ¶È:52%
Bioorganic & Medicinal Chemistry          1996          4          1909-1918
N-tetrachlorophthaloyl (TCP) for ready protection/deprotection of amino sugar glycosides
John S Debenham, Sheryl D Debenham, Bert Fraser-Reid
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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37 .     (4R)-3-[(2R,3R)-2,6-Bis(benzyloxy)-3-hydroxy-2-methylhexanoyl]-5,5-dimethyl-4-phenyloxazolidin-2-one
C32H37NO6     ÏàËÆ¶È:52%
European Journal of Organic Chemistry          2012                   988-994
Towards Allopumiliotoxins: A Concise Synthesis of the Indolizidine Core
Bodduri V. D. Vijaykumar, Pitchakuntla Mallesham and Srivari Chandrasekhar
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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38 .     1-[2,2-dimethyl-8,8a-dihydro-3aH-indeneo[(1S,2R)-1,2]-oxazol-3-yl] (2R)-benzyl-3-benzyloxy propanone
C29H31NO3     ÏàËÆ¶È:52%
Bioorganic & Medicinal Chemistry          2010          18          2037-2048
Design, asymmetric synthesis, and evaluation of pseudosymmetric sulfoximine inhibitors against HIV-1 protease
Ding Lu, Yuk Yin Sham, Robert Vince
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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39 .     methyl (1R,3R,4R,5S)-5-acetamido-1-benzyloxy-4-(tert-butoxycarbonylamino)-3-(2-tosyloxyethoxy)-cyclohexane-1-carboxylate
C31H42N2O10S     ÏàËÆ¶È:52%
Bioorganic & Medicinal Chemistry          2010          18          7239-7251
Design, synthesis, biological evaluation, and modeling of a non-carbohydrate antagonist of the myelin-associated glycoprotein
Oliver Schwardt, Hendrik Koliwer-Brandl, Raphael Zimmerli, Stefanie Mesch, Gianluca Rossato, Morena Spreafico, Angelo Vedani, Sørge Kelm, Beat Ernst
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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40 .     Compound 10
C39H50N8O5     ÏàËÆ¶È:51.8%
Bioorganic & Medicinal Chemistry Letters          2009          19          6736-6739
Design, synthesis and biological evaluation of a bivalent ¦Ì opiate and adenosine A1 receptor antagonist
Smitha C. Mathew, Nandita Ghosh, Youlet By, Aur¨¦lie Berthault, Marie-Alice Virolleaud, Louis Carrega, Gaëlle Chouraqui, Laurent Commeiras, Jocelyne Condo, Mireille Attolini, Anouk Gaudel-Siri, Jean Ruf, Jean-Luc Parrain, Jean Rodriguez, R¨¦gis Guieu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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41 .     cuneataside E
C24H40O11     ÏàËÆ¶È:50%
Phytochemistry          2005          66          2752-2758
Phenolic glycosides and ionone glycoside from the stem of Sargentodoxa cuneata
Jun Chang, Ryan Case
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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42 .     ugonstilbene A
C24H28O3     ÏàËÆ¶È:50%
Planta Medica          2003          69          964-967
Cyclized Geranyl Stilbenes from the Rhizomes of Helminthostachys zeylanica
Chien-Chih Chen,Yu-Ling Huang,Pei-Yu Yeh,Jun-Chih Ou
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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43 .     3,3a-Dibutyl-3,3a,5,9b-tetrahydro-9b-hydroxy-5-methyl-1-phenyl-1H-imidazo[4,5-c]quinoline-2,4-dione
C25H31N3O3     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2009          92          689-708
Molecular Rearrangement of 9b-Hydroxy-1H-imidazo[4,5-c]quinoline-2,4-diones - A Convenient Pathway to Spiro-Linked Imidazolidine-Oxindole Derivatives
Anton¨ªn Kl¨¢sek, Anton¨ªn Lyčka, Ivan Mikš¨ªk, Aleš Růička
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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44 .     3,3a-Dibutyl-3,3a,5,9b-tetrahydro-9b-hydroxy-1,5-diphenyl-1H-imidazo[4,5-c]quinoline-2,4-dione
C30H33N3O3     ÏàËÆ¶È:50%
Helvetica Chimica Acta          2009          92          689-708
Molecular Rearrangement of 9b-Hydroxy-1H-imidazo[4,5-c]quinoline-2,4-diones - A Convenient Pathway to Spiro-Linked Imidazolidine-Oxindole Derivatives
Anton¨ªn Kl¨¢sek, Anton¨ªn Lyčka, Ivan Mikš¨ªk, Aleš Růička
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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45 .     N-(L-Phenylalanine methyl ester)sulfonyl-L-proline benzyl ester
C22H27N2O6S     ÏàËÆ¶È:50%
Molecules          2007          12          1125-1135
Synthesis of Sulfonamides and Evaluation of Their Histone Deacetylase (HDAC) Activity
Seikwan Oh, Hyung¨CIn Moon, Il¨CHong Son and Jae¨CChul Jung
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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46 .     2-Phenylethyl-6-O-[ (E)-cin-namoyl ]-¦Â-D-glucopyranoside
    ÏàËÆ¶È:50%
Journal of Chinese Pharmaceutical Sciences          2004          13          14-18
Synthesis of Phenylpropanoid Glycoside Analogs
LI Shu-chun, ZHOU Jing, and LI Zhong-jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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47 .     compound IV
    ÏàËÆ¶È:50%
Acta Pharmaceutica Sinica          1992          27          279-282
STUDIES ON NAPHTHOIC ACID ESTERS FROM THE ROOTS OF RUBIA CORDIFOLIA L.
HM Hua; SX Wang; LJ Wu; X Li; TR Zhu
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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48 .     De-A,B-22-benzenesulphonyl-23,24-dinorcholestan-8-benzyloxymethyl ether
    ÏàËÆ¶È:50%
Steroids          2000          65          252-265
Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3
Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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49 .     De-A,B-24,25-dihydroxy-cholestan-8-benzyloxymethylether
C18H33O2     ÏàËÆ¶È:50%
Steroids          2000          65          252-265
Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3
Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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50 .     De-A,B-24-oxo-25-hydroxy-cholestan-8-benzyloxymethyl ether
C18H31O3     ÏàËÆ¶È:50%
Steroids          2000          65          252-265
Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3
Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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51 .     De-A,B-24-oxo-23,25-dihydroxy cholestan-8-benzyloxymethyl ether
C18H31O3     ÏàËÆ¶È:50%
Steroids          2000          65          252-265
Synthesis and biological activities of the two C(23) epimers of 1¦Á,23,25-trihydroxy-24-oxo-19-nor-vitamin D3: novel analogs of 1¦Á,23(S),25-trihydroxy-24-oxo-vitamin D3, a natural metabolite of 1¦Á,25-dihydroxyvitamin D3
Nancy E. Lee, Paul G. Williard, Alex J. Brown, Moray J. Campbell, H. Phillip Koeffler, Sara Peleg, D. Sunita Rao, G. Satyanarayana Reddy
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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52 .     3-Benzyloxy-13¦Á-estra-1,3,5(10)-trien-17-one
    ÏàËÆ¶È:50%
Steroids          2003          68          277-288
Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers
J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, Éva Frank, George Falkay, Árp¨¢d M¨¢rki, Ren¨¢ta Minorics, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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53 .     3-benzyloxy-16¦Â-hydroxymethyl-13¦Á-estra-1,3,5(10)-trien-17¦Á-ol
C26H32O3     ÏàËÆ¶È:50%
Steroids          2003          68          277-288
Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers
J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, Éva Frank, George Falkay, Árp¨¢d M¨¢rki, Ren¨¢ta Minorics, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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54 .     3-benzyloxy-16¦Â-acetoxymethyl-13¦Á-estra-1,3,5(10)-trien-17¦Á-ol
C28H34O4     ÏàËÆ¶È:50%
Steroids          2003          68          277-288
Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers
J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, Éva Frank, George Falkay, Árp¨¢d M¨¢rki, Ren¨¢ta Minorics, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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55 .     16,17-seco-3-Benzyloxy-13¦Á-estra-1,3,5(10),16-tetraen-17-al
C26H30O2     ÏàËÆ¶È:50%
Steroids          2003          68          277-288
Synthesis and receptor-binding examinations of the normal and 13-epi-D-homoestrones and their 3-methyl ethers
J¨¢nos Wölfling, Erzs¨¦bet Merny¨¢k, Éva Frank, George Falkay, Árp¨¢d M¨¢rki, Ren¨¢ta Minorics, Gyula Schneider
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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56 .     butylrolactone-V
C24H24O8     ÏàËÆ¶È:50%
Natural Product Research          2009          23          77-85
Secondary metabolites of Aspergillus sp. F1, a commensal fungal strain of Trewia nudiflora
Ting Lin; Chunhua Lu; Yuemao Shen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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