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1 .     rhazizine
C21H24N2O4     ÏàËÆ¶È:71.4%
Tetrahedron          1989          45          3507-3512
Rhazizine: A novel alkaloid from the leaves of Rhazya stricta
Atta-ur-Rahman, Talat Fatima, Sajida Khanum
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     pyrrolidinoindoline
C24H27N3O2     ÏàËÆ¶È:59.0%
Organic Letters          2008          Vol.10,No.1          125-128
First Total Synthesis of Trimeric Indole Alkaloid, Psychotrimine

Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     5-((4-heptylphenyl)ethynyl)-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one
    ÏàËÆ¶È:59.0%
Bioorganic & Medicinal Chemistry          2010          18          5826-5834
Improved inhibition of the histone acetyltransferase PCAF by an anacardic acid derivative
Massimo Ghizzoni, Andr¨¦ Boltjes, Chris de Graaf, Hidde J. Haisma, Frank J. Dekker
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     10-demetlwxy-1-norvincorine N-oxide
C20H24N2O3     ÏàËÆ¶È:57.1%
Planta Medica          1988          54          214-218
Relative Configuration and Cytotoxic Activity of Vincarubine: A Novel Bisindole Alkaloid from Vinca minor
B. Proksat, D. Uhrfn, E. Grossmann, Z. Votickt, and J. Fuska
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     Aspernolide A
C24H24O7     ÏàËÆ¶È:57.1%
Phytochemistry          2009          70          128-132
Aspernolides A and B, butenolides from a marine-derived fungus Aspergillus terreus
Rajesh R. Parvatkar, Celina D¡¯Souza, Ashootosh Tripathi, Chandrakant G. Naik
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     vomilenine
    ÏàËÆ¶È:57.1%
Phytochemistry          1996          41          969-973
Indole alkaloids from Rauwolfia sellowii
Cesar Vicente Ferreira Batista, Jan Schripsema, Robert Verpoorte, Sandra Beatriz Rech, Amelia T. Henriques
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     acidissiminol epoxide
C25H31NO4     ÏàËÆ¶È:57.1%
Phytochemistry          1994          37          757-760
Dihydroxy acidissiminol and acidissiminol epoxide, two tyramine derivatives from Limonia acidissima
Parthasarathi Ghosh, Mrinal Kanti Ghosh, Swapnadip Thakur, Jasodhara dan (Datta), Toshihiro Akihisa, Toshitake Tamura, Yumiko Kimura
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     3-methoxy-1-(3-methylphenyl)-4-phenyl-3,4-dihydro-1H-2-benzothiopyran
C23H21NOS     ÏàËÆ¶È:57.1%
Heterocycles          2008          75          3025-3033
Synthesis of 1-Iminoisothiochroman Derivatives Based on Reactions of 2-Lithio-¦Â-methoxystyrene Derivatives with Isothiocyanates Followed by Acid-mediated Cyclization
Kazuhiro Kobayashi, Daisuke Nakai, Kazutaka Hayashi, and Hisatoshi Konishi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     diethyl 2-[4-(methoxycarbonylmethyl)-3-phenyl-3,4-dihydroquinazolin-2-yl]propanedioate
C24H26N2O6     ÏàËÆ¶È:57.1%
Heterocycles          2012          84          893-911
Expedient Synthesis of 3,4-Dihydroquinazolines via Tandem Addition ¡ª Conjugate Addition Cyclization of Carbodiimides Bearing a Michael Acceptor
Takao Saito,* Hayato Nakano, Hidenori Terada, Noriki Kutsumura, and Takashi Otani
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     5,14-Dihydro-5,6-dimethyl-6,14-methano-6H-benzo[d]naphtho[1,2-g][1,3]oxazocine
C21H19NO     ÏàËÆ¶È:57.1%
Helvetica Chimica Acta          2011          94          142-147
A Facile Synthesis of Bridged Polycyclic Naphthooxazocine Skeletons: Eight-Membered-Ring Constructions via Tandem Dinucleophilic Addition of Naphthalenols to Quinolinium Salts
Firouz Matloubi Moghaddam, Salman Taheri, Zohreh Mirjafary, Hamdollah Saeidian, Mostafa Kiamehr and Mohsen Tafazzoli
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     S-(3-Butyl-1,2,3,4-tetrahydro-2,4-dioxo-1-phenylquinolin-3-yl) Carbamothioate
C20H20N2O3S     ÏàËÆ¶È:57.1%
Helvetica Chimica Acta          2012          95          1352-1372
Modified Riemschneider Reaction of 3-Thiocyanatoquinolinediones
Ondřej Rudolf, Vladim¨ªr Mrkvička, Anton¨ªn Lyčka, Michal Rouchal and Anton¨ªn Kl¨¢sek
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     herbamine
    ÏàËÆ¶È:54.5%
Chemistry of Natural Compounds          1982          18          693-696
NMR INVESTIGATION OF ALKALOIDS.III. 13C NMR SPECTRA AND RECONSIDERATION OF THEn STEREOCHEMISTRY OF HERBAMINE AND HERBADINE
M. R. Yagudaev
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     11-butyl-4-chloro-10-(2-methoxyphenyl)-7,8,10,11-tetrahydro-5H-benzo[e] pyrimido[4,5-b][1,4]diazepin-9(6H)-one
    ÏàËÆ¶È:54.5%
Journal of Heterocyclic Chemistry          2010          47          990-993
Synthesis of novel tricyclic 4-chloro-7,8,10,11-tetrahydro-5H-benzo[e]pyrimido[4,5-b][1,4]diazepin-9(6H)-ones
Jinbao Xiang, Lianyou Zheng, Tong Zhu, Qun Dang and Xu Bai
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 2a
    ÏàËÆ¶È:54.5%
Tetrahedron Letters          2005          46          8153-8157
Linear C2-symmetric polycyclic benzodithiophene: efficient, highly diversified approaches and the optical properties
Cui-Hua Wang, Rong-Rong Hu, Shuang Liang, Jia-Hua Chen, Zhen Yang, Jian Pei
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     18,19-dehydrocorynoxinic acid
C21H24N2O4     ÏàËÆ¶È:52.3%
Journal of Natural Products          2008          71(7)          1271-1274
Alkaloids from the Leaves of Uncaria rhynchophylla and Their Inhibitory Activity on NO Production in Lipopolysaccharide-Activated Microglia
Dan Yuan, Bin Ma, Chunfu Wu, Jingyu Yang, Lijia Zhang, Suiku Liu, Lijun Wu, and Yoshihiro Kano
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     compound 2a
C27H38O4     ÏàËÆ¶È:52.3%
Journal of Natural Products          2007          70          1249-1252
Hydroxyalkenylresorcinols from Stylogyne turbacensis
Carlos Jim¨¦nez-Romero, Daniel Torres-Mendoza, Luis David Ureña Gonz¨¢lez, Eduardo Ortega-Barr¨ªa,Kerry L. McPhail,William H. Gerwick, and Luis Cubilla-Rios
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     rhazicine N-oxide
    ÏàËÆ¶È:52.3%
Planta Medica          1988          54          235-236
The Alkaloids of Melodinus acutiflorus. Rhazicine N-Oxide
Wen-lan Hu and Manfred Hesse
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     herbamine
C22H26N2O4     ÏàËÆ¶È:52.3%
Chemistry of Natural Compounds          1996          32          216-334
ALKALOIDS. PLANTS, STRUCTURE, PROPERTIES
R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     2-Bromo-N-[4-(3-{[6-( 3,5-dimethylbenzyl)-5-ethyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl]methoxy}prop-1-ynyl)phenyl]acetamide
C27H28BrN3O4     ÏàËÆ¶È:52.3%
Helvetica Chimica Acta          2009          92          1385-1403
Synthesis and Anti-HIV-1 Evaluation of New Sonogashira-Modified Emivirine (MKC-442) Analogues
Krzysztof Danel, Per T. Jørgensen, Erik B. Pedersen, Paolo La Colla, Gabriella Collu, Roberta Loddo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     6-(3,5-Dimethylbenzyl)-5-ethyl-1-[({3-[4-(hydroxymethyl)phenyl]prop-2-ynyl}oxy)methyl]uracil
C25H26N2O4     ÏàËÆ¶È:52.3%
Helvetica Chimica Acta          2009          92          1385-1403
Synthesis and Anti-HIV-1 Evaluation of New Sonogashira-Modified Emivirine (MKC-442) Analogues
Krzysztof Danel, Per T. Jørgensen, Erik B. Pedersen, Paolo La Colla, Gabriella Collu, Roberta Loddo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2013-08-24 11:11:46
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