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1 .     4-N,N-dimethyl-3'-methoxy-stilbene
C17H19NO     ÏàËÆ¶È:61.5%
Bioorganic & Medicinal Chemistry          2010          18          7724-7730
Synthesis and evaluation of stilbene derivatives as a potential imaging agent of amyloid plaques
Myeng Chan Hong, Yun Kyung Kim, Jae Yong Choi, Si Qiang Yang, Hakjune Rhee, Young Hoon Ryu, Tae Hyun Choi, Gi Jeong Cheon, Gwang Il An, Hye Yun Kim, Youngsoo Kim, Dong Jin Kim, Jun-Seok Lee, Young-Tae Chang, Kyo Chul Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

2 .     4-N-methyl-2'-methoxy-stilbene
C15H14BrN     ÏàËÆ¶È:61.5%
Bioorganic & Medicinal Chemistry          2010          18          7724-7730
Synthesis and evaluation of stilbene derivatives as a potential imaging agent of amyloid plaques
Myeng Chan Hong, Yun Kyung Kim, Jae Yong Choi, Si Qiang Yang, Hakjune Rhee, Young Hoon Ryu, Tae Hyun Choi, Gi Jeong Cheon, Gwang Il An, Hye Yun Kim, Youngsoo Kim, Dong Jin Kim, Jun-Seok Lee, Young-Tae Chang, Kyo Chul Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

3 .     4-N-methyl-3'-methoxy-stilbene
C15H14BrN     ÏàËÆ¶È:61.5%
Bioorganic & Medicinal Chemistry          2010          18          7724-7730
Synthesis and evaluation of stilbene derivatives as a potential imaging agent of amyloid plaques
Myeng Chan Hong, Yun Kyung Kim, Jae Yong Choi, Si Qiang Yang, Hakjune Rhee, Young Hoon Ryu, Tae Hyun Choi, Gi Jeong Cheon, Gwang Il An, Hye Yun Kim, Youngsoo Kim, Dong Jin Kim, Jun-Seok Lee, Young-Tae Chang, Kyo Chul Lee
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

4 .     lynamicin C
C20H11N3Cl4     ÏàËÆ¶È:58.3%
Journal of Natural Products          2008          71(10)          1732-1737
Lynamicins A-E, Chlorinated Bisindole Pyrrole Antibiotics from a Novel Marine Actinomycete
Katherine A. McArthur, Scott S. Mitchell, Ginger Tsueng, Arnold Rheingold,Donald J. White, Jennifer Grodberg, Kin S. Lam, and Barbara C. M. Potts
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

5 .     keramidine
    ÏàËÆ¶È:58.3%
Journal of Natural Products          2005          68          327-330
Dominicin, a Cyclic Octapeptide, and Laughine, a Bromopyrrole Alkaloid, Isolated from the Caribbean Marine Sponge Eurypon laughlini
David E. Williams, Brian O. Patrick, Hans W. Behrisch, Rob Van Soest, Michel Roberge, and Raymond J. Andersen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

6 .     mukanadin A
C11H13N5O3Br     ÏàËÆ¶È:58.3%
Journal of Natural Products          1999          62          1581-1583
Mukanadins A-C, New Bromopyrrole Alkaloids from Marine Sponge Agelas nakamurai
Hiroshi Uemoto, Masashi Tsuda, and Jun¡¯ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

7 .     6-oxo-6¦Ã(5)-dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl-diethyl-1H-2-imida-zolyl aminomethylphosphonate
C20H23N3O6P2     ÏàËÆ¶È:58.3%
Chemical & Pharmaceutical Bulletin          2009          57          1391-1395
One-Step Synthesis and Bioassay of N-Phosphoramidophosphonates
Mudumala Veera Narayana Reddy, Avula Balakrishna, Mungara Anil Kumar, Gangireddygari Chandra Sekhar Reddy, Arigela Uma Ravi Sankar, Cirandur Suresh Reddy and Tirupati Murali Krishna
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

8 .     3RS(3R,4R,5S)-2,5-diphenyl-3-furyl-4-nitroisoxazolidine
C19H16N2O4     ÏàËÆ¶È:58.3%
Journal of Heterocyclic Chemistry          2007          44          1045-1049
1,3-dipolar cycloadditions. Part XII-selective cycloaddition route to 4-nitroisoxazolidine ring systems
Avijit Banerji,Maya Gupta,Pizush Kanti Biswas,Thierry Prang¨¦ and Alain Neuman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

9 .     compound 9
    ÏàËÆ¶È:58.3%
Journal of Heterocyclic Chemistry          2005          42          867-875
A study of substituent effect on 1H and 13C NMR spectra of mono,di and poly substituted carbazoles
Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

10 .     compound 3c
    ÏàËÆ¶È:58.3%
Journal of Heterocyclic Chemistry          2004          41          161-171
A study of substituent effect on 1H and 13C nmr spectra of N-and C-substituted carbazoles
Sergio M. Bonesi,Maria A. Ponce and Rosa Erra-Balsells
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

11 .     1-phenyl-3,4-dihydro-9H-¦Â-carboline
C17H14N2     ÏàËÆ¶È:58.3%
Heterocycles          2005          65          2483-2492
A Simple Method for the Synthesis of 1-Substituted ¦Â-Carboline Derivatives from Tryptamine and Carboxylic Acids in Polyphosphoric Acid
Iliyan Ivanov,* Stoyanka Nikolova, and Stela Statkova-Abeghe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

12 .     1-(3',4'-dimethoxyphenyl)-3,4-dihydro-9H-¦Â-carboline
C19H18N2O2     ÏàËÆ¶È:58.3%
Heterocycles          2005          65          2483-2492
A Simple Method for the Synthesis of 1-Substituted ¦Â-Carboline Derivatives from Tryptamine and Carboxylic Acids in Polyphosphoric Acid
Iliyan Ivanov,* Stoyanka Nikolova, and Stela Statkova-Abeghe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

13 .     1-(2'-naphthyl)-3,4-dihydro-9H-¦Â-carboline
C21H16N2     ÏàËÆ¶È:58.3%
Heterocycles          2005          65          2483-2492
A Simple Method for the Synthesis of 1-Substituted ¦Â-Carboline Derivatives from Tryptamine and Carboxylic Acids in Polyphosphoric Acid
Iliyan Ivanov,* Stoyanka Nikolova, and Stela Statkova-Abeghe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

14 .     Compound 8a
C11H10N2S2     ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry Letters          2006          16          6273-6276
Isobrassinin and its analogues: Novel types of antiproliferative agents
P¨¦ter Csom¨®s, Istv¨¢n Zupk¨®, Borb¨¢la R¨¦thy, Lajos Fodor, George Falkay, G¨¢bor Bern¨¢th
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

15 .     N-chloromethyl-N,N-dimethyl tryptamine
C13H18ClN2     ÏàËÆ¶È:58.3%
Magnetic Resonance in Chemistry          2007          45          359-361
NMR spectral assignments of a new chlorotryptamine alkaloid and its analogues from Acacia confusa (pages 359¨C361)
Malcolm S. Buchanan, Anthony R. Carroll, David Pass and Ronald J. Quinn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

16 .     hymenidin
    ÏàËÆ¶È:58.3%
Tetrahedron          1990          46          5579-5586
Ageliferins, potent actomyosin Atpase activators from the Okinawan marine sponge Agelas sp
Jun'ichi Kobayashi, Masashi Tsuda, Tetsuya Murayama, Hideshi Nakamura, Yasushi Ohizumi, Masami Ishibashi, Michiko Iwamura, Tomihisa Ohta, Shigeo Nozoe
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

17 .     diethyl 2,6-dihydroxy-4-(3-thienyl)-2,6-bis(trifluoromethyl)tetrahydro-2H-pyran-3,5-dicarboxylate
C17H18F6SO7     ÏàËÆ¶È:58.3%
Russian Journal of Organic Chemistry          2010          46          468-473
Synthesis of 2,6-bis(fluoroalkyl)-2,6-dihydroxytetrahydro-2H-pyran-3,5-dicarboxylates from aldehydes and fluorinated ¦Â-oxo esters in the presence of ionic liquid-K2CO3 as catalytic system
S. G. Zlotin, G. V. Kryshtal¡¯, G. M. Zhdankina, A. V. Ignatenko and Ya. V. Burgart, et al.
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

18 .     hymenidin
C11H12N5OBr     ÏàËÆ¶È:58.3%
Experientia          1986          42          1176-1177
A novel antagonist of serotonergic receptors, hymenidin, isolated from the Okinawan marine spongeHymeniacidon sp.
J. Kobayashi, Y. Ohizumi, H. Nakamura and Y. Hirata
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

19 .     2-morpholin-4-yl-5-phenyl-pyridine-3-carbonitrile
C16H15N3O     ÏàËÆ¶È:58.3%
Tetrahedron          2012          68          10318-10325
An alternative synthesis of pyrimido[4,5-b]quinoline-4-ones via metal-free amination in water and Vilsmeier¨CHaack cyclization
Radhey M. Singh, Neha Sharma, Ritush Kumar, Mrityunjaya Asthana, Shraddha Upadhyay
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

20 .     ethyl 2,2-difluoro-2-(4-phenoxyphenyl)acetate
C16H14F2O3     ÏàËÆ¶È:58.3%
Tetrahedron          2013          69          3913-3918
Cobalt-catalyzed cross-coupling reaction of arylzinc reagents with ethyl bromodifluoroacetate
Keisuke Araki, Munenori Inoue
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

21 .     compound 8i
C15H14BNO5     ÏàËÆ¶È:58.3%
Tetrahedron          2013          69          7732-7740
(1-Bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis
Eric M. Woerly, Jonathan E. Miller, Martin D. Burke
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

22 .     1-methyl-1H-benzo[d]imidazole-2-carbonitrile
    ÏàËÆ¶È:58.3%
Organic Magnetic Resonance          1982          20          212-216
Investigation of benzimidazoles. III¡ªtransmission of the substituent effects in 2-substituted 1-methylbenzimidazoles studied by 13C nuclear magnetic resonance
V. A. Lopyrev, L. I. Larina, T. I. Vakul'skaya, E. F. Shibanova, I. A. Titova, M. G. Voronkov and E. E. Liepin'sh
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

23 .     9-methoxy derivative of monobromodispacamide
C12H14BrN5O3     ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry          2006          14          17-24
Novel bioactive bromopyrrole alkaloids from the Mediterranean sponge Axinella verrucosa
Anna Aiello, Monica D¡¯Esposito, Ernesto Fattorusso, Marialuisa Menna, Werner E.G. M¨¹ller, Sanja Perović-Ottstadt, Heinz C. Schröder
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

24 .     2-(1H-Indol-3-yl)-4-thiazolecarboxylic acid
C12H8N2O2S     ÏàËÆ¶È:58.3%
Bioorganic & Medicinal Chemistry          2013          21          4541-4549
Metabolism of the phytoalexins camalexins, their bioisosteres and analogues in the plant pathogenic fungus Alternaria brassicicola
M. Soledade C. Pedras, Abbas Abdoli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

25 .     (Z)-4-(Benzofuran-3-ylmethylene)-1-methyl-2-(methylthio)-1H-imidazol-5(4H)-one
C14H12N2O2S     ÏàËÆ¶È:57.1%
Molecules          2011          16          5527-5537
Microwave Assisted Synthesis of Novel Functionalized Hydantoin Derivatives and Their Conversion to 5-(Z)Arylidene-4H-imidazoles
Sukanta Kamila, Haribabu Ankati and Edward R. Biehl
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

26 .     konbamidin
C13H14N2O4     ÏàËÆ¶È:53.8%
Journal of Natural Products          1994          Vol 57          1603
Konbamidin, a New Indole Alkaloid from the Okinawan Marine Sponge Ircinia sp.
Hideki Shinonaga, Hideyuki Shigemori, Jun'ichi Kobayashi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

27 .     4',4'''-Dihydroxy-6,6''-diflavone
C30H18O6     ÏàËÆ¶È:53.8%
Bioorganic & Medicinal Chemistry          2011          19          3060-3073
Synthesis and antifungal activities of natural and synthetic biflavonoids
Gabriel Sagrera ,Ana Bertucci, Alvaro Vazquez, Gustavo Seoane
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

28 .     3-((1H-Indol-3-yl)(phenyl)methyl)-1H-indole
C23H18N2     ÏàËÆ¶È:53.8%
Canadian Journal of Chemistry          2009          87          416-421
A catalyst-free protocol for the green and efficient condensation of indoles with aldehydes in ionic liquids
Abdolkarim Zare, Abolfath Parhami, Ahmad Reza Moosavi-Zare,Alireza Hasaninejad, Ali Khalafi-Nezhad, and Mohammad Hassan Beyzavi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

29 .     3-((1H-Indol-3-yl)(phenyl)methyl)-1H-indole
    ÏàËÆ¶È:53.8%
Canadian Journal of Chemistry          2007          85          416-420
A solvent-free protocol for facile condensation of indoles with carbonyl compounds using silica chloride as a new, highly efficient, and mild catalyst
Alireza Hasaninejad, Abdolkarim Zare, Hashem Sharghi, Mohsen Shekouhy,Reza Khalifeh, Alireza Salimi Beni, and Ahmad Reza Moosavi Zare
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
--------------------------------------------------------------------------------

30 .     3,3'-Bis(5-bromo-indolyl)phenylmethane
C23H16Br2N2     ÏàËÆ¶È:53.8%
Canadian Journal of Chemistry          2006          84          1541-1545
Efficient RuIII-catalyzed condensation of indoles and aldehydes or ketones
Khalil Tabatabaeian, Manouchehr Mamaghani, Nosratollah Mahmoodi, and Alireza Khorshidi
Tobeastriver
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