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331456351

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13C NMR (151 MHz, CCl3) ¦Ä, 13.06,30.20,41.43, 56.96,108.62,109.85, 129.06,134.39,142.71,  160.58, 160.83, 161.63,  184.60,177.95, 204.00
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1 .     2-acetonyl-3-methyl-7-methoxy-naphthazarin
C15H14O6     ÏàËÆ¶È:93.3%
Natural Product Research and Development          2009          21          574-576
Naphthaquinones from Fusarium sp. 1RGa-1b,an Endophytic Fungus Associated with Trewia nudiflora(Euphorbiaceae)
YU Bu-zhu;SONG Cheng-zhi;DU Zhi-zhi; CAI Xiang-hai; HUANG Sheng-xiong; LUO Xiao-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     (1S,3R)-austrocortirubin
C16H16O7     ÏàËÆ¶È:60%
Australian Journal of Chemistry          1999          52          1115-1117
Pigments of Fungi. LXII. (1S,3R)-Austrocortirubin: Isolation from the Fungus Dermocybe splendida and Synthesis from (S)-Citramalic Acid
Catherine Elsworth, Melvyn Gill and Abilio Ten
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     70 -amino-20 - methyl-2,40 -dioxo-30 ,40 -dihydrospiro[indoline-3,50 -pyrano[2, 3-d]pyrimidine]-60 -carbonitrile
C16H11N5O3     ÏàËÆ¶È:56.2%
Journal of Heterocyclic Chemistry          2009          46          1266-1270
An efficient,three-component synthesis of spiro[benzo[g]chromene-4,3'-indoline]-3-carbonitrile and spiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile derivatives
Ramin Ghahremanzadeh,Tayebeh Amanpour and Ayoob Bazgir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     7'-amino-4'-hydroxy-2'-methyl-2-oxospiro[indoline-3,5'-pyrano[2,3-d]pyrimidine]-6'-carbonitrile
C16H11N5O3     ÏàËÆ¶È:56.2%
Journal of Heterocyclic Chemistry          2010          47          967-972
One-pot and three-component synthesis of spiro[chromeno[2,3-d] pyrimidine-5,3'-indoline]-diones and spiro[chromeno[2,3-c] pyrazole-4,3'-indoline]-diones
Ramin Ghahremanzadeh, Fatemeh Fereshtehnejad, Zahra Yasaei, Tayebeh Amanpour and Ayoob Bazgir
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     5,7-Dimethoxyflavone
     ÏàËÆ¶È:53.3%
Phytochemistry          1994          35          765-768
Triterpenoids and flavonoids from Leptospermum scoparium
Hanns Häberlein, Klaus-P. Tschiersch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     N-(4-phenyl-thiazol-2-yl)-2-(p-methoxyphenylhydrazono)-2-cyanoacetamide
C19H15N5O2S     ÏàËÆ¶È:53.3%
Journal of Heterocyclic Chemistry          2003          40          963-971
Versatile 2-aminothiazoles,building blocks for highly functionalised heterocycles
Gerd Kaupp,Fathy A. Amer,Mohamed Abbas Metwally and Ehab Abdel-Latif
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     6-ethyl-5-hydroxy-2,7-dimethoxy-1,4-naphthoquinone
     ÏàËÆ¶È:53.3%
Chinese Pharmaceutical Journal          2008          43          255-257
Study on the Antiphlogistic Constituents in Seed of Schisandra propinqua(Wall)Hook.f.et Thoms
LI Jun, LI Fu, LU Yuan-yuan, WEN Gui-qing, SU Xiao-jian
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     2-isopropanol-3-methyl-7-methoxy-naphthazarin
C15H16O6     ÏàËÆ¶È:53.3%
Natural Product Research and Development          2009          21          574-576
Naphthaquinones from Fusarium sp. 1RGa-1b,an Endophytic Fungus Associated with Trewia nudiflora(Euphorbiaceae)
YU Bu-zhu;SONG Cheng-zhi;DU Zhi-zhi; CAI Xiang-hai; HUANG Sheng-xiong; LUO Xiao-dong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     6-ethyl-5-hydroxy-2,7-dimethoxy-1,4-naphthoquninone
     ÏàËÆ¶È:53.3%
Bioorganic Chemistry          1981          10          399-411
6-Ethyl-5-hydroxy-2,7-dimethoxy-1,4-naphthoquinone from Hendersonula toruloidea: A biosynthetic study using 13C labels detected by nuclear magnetic resonance and 14C tracers
Ronald Bentley, W.J. Banach, A.Gavin McInnes, John A. Walter
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     3-ethyl-4-ethylsulfanyl-8-methoxyisoquinolin-1(2H)-one
C14H17NO2S     ÏàËÆ¶È:53.3%
Heterocycles          2012          85          887-894
Synthesis of 3-Substituted 4-Sulfanyl-8-methoxyisoquinolin-1(2H)-ones by the Reaction of Ethyl 2-[Lithio(sulfanyl)methyl]-6-methoxybenzoates with Aliphatic and Aromatic Nitriles
Kazuhiro Kobayashi,* Hiroo Hashimoto, and Kazuhiro Nakagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     4-ethylsulfanyl-8-methoxy-3-(1-methylethyl)isoquinolin-1(2H)-one
C15H19NO2S     ÏàËÆ¶È:53.3%
Heterocycles          2012          85          887-894
Synthesis of 3-Substituted 4-Sulfanyl-8-methoxyisoquinolin-1(2H)-ones by the Reaction of Ethyl 2-[Lithio(sulfanyl)methyl]-6-methoxybenzoates with Aliphatic and Aromatic Nitriles
Kazuhiro Kobayashi,* Hiroo Hashimoto, and Kazuhiro Nakagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     5,4'-dimethoxyflavone
C17H14O4     ÏàËÆ¶È:53.3%
Journal of Medicinal Chemistry          1995          38          4937-4943
Synthesis and Biological Evaluation of Substituted Flavones as Gastroprotective Agents
Jeffrey J. Ares, Pamela E. Outt, Jared L. Randall, Peter D. Murray, Pamela S. Weisshaar, Linda M. O'Brien, Beth L. Ems, Sunil V. Kakodkar, Gary R. Kelm,
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     5-¼×Ñõ»ù»ÆÍª
    ÏàËÆ¶È:53.3%
Journal of Chinese Medicinal Materials          2010          33          1871-1874
Chemical Constituents of Rhizoma Imperatae and Their Anti-complementary Activity
FU Li-na, CHEN Lan-ying, LIU Rong-hua, CHEN Dao-feng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     5,7-Dimethoxy-8-(3-hydroxy-3-methylbut-1Z-enyl)flavone (= Z-tephrostachin)
C22H22O5     ÏàËÆ¶È:52.9%
Phytochemistry          2012          78          135-146
Distinct chemotypes of Tephrosia vogelii and implications for their use in pest control and soil enrichment
Philip C. Stevenson, Geoffrey C. Kite, Gwilym P. Lewis, F¨¦lix Forest, Stephen P. Nyirenda,Steven R. Belmain, Gudeta W. Sileshi, Nigel C. Veitch
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     trans-Tephrostachin
C22H22O5     ÏàËÆ¶È:52.9%
Phytochemistry          1981          20          1719-1720
8-C-Prenylflavonoids from the seed of Tephrosia bracteolata
Sami A. Khalid, Peter G. Waterman
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     (+)-austrocortirubin
C16H16O7     ÏàËÆ¶È:50%
Journal of the Chemical Society, Perkin Transactions 1          1990                   1583-1592
Pigments of fungi. Part 12. Structure and absolute stereochemistry of antibiotic tetrahydroanthraquinones from the fungus Dermocybe splendida Horak. X-Ray structure determination of austrocortirubin phenylboronate and austrocortilutein acetonide
Melvyn Gill, Albin F. Smrdel, Richard J. Strauch and Michael J. Begley
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     nigrosporin B
C16H16O6     ÏàËÆ¶È:50%
Bioscience, Biotechnology, and Biochemistry          1997          61          1848-1852
Nigrosporins A and B, New Phytotoxic and Antibacterial Metabolites Produced by a Fungus Nigrospora oryzae
Masayasu TANAKA, Toshiro FUKUSHIMA, Yasuko TSUJINO, Takane FUJIMORI
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     4-ethylsulfanyl-8-methoxy-3-phenylisoquinolin-1(2H)-one
C18H17NO2S     ÏàËÆ¶È:50%
Heterocycles          2012          85          887-894
Synthesis of 3-Substituted 4-Sulfanyl-8-methoxyisoquinolin-1(2H)-ones by the Reaction of Ethyl 2-[Lithio(sulfanyl)methyl]-6-methoxybenzoates with Aliphatic and Aromatic Nitriles
Kazuhiro Kobayashi,* Hiroo Hashimoto, and Kazuhiro Nakagawa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     3-Omethylfusarubin
C16H16O7     ÏàËÆ¶È:50%
Acta Scientiarum Naturalium Universitatis Sunyatseni          2008          47(1)          56-58
Secondary Metabolites of Mangrove Endophytic Fungus B77 in the South China Sea
SHAO Chang-lun, HU Gu-ping, YANG Rui-yun, XIA Xue-kui, WANG Chang-yun, SHE Zhi-gang, LIN Yong-cheng
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2Â¥2013-11-22 21:30:35
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