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22.06,22.86,23.15,24.69,30.11,35.47,39.16,50.58,55.06,102.47,111.16,111.42,118.94,119.17,120.20,121.74,122.95,127.17,128.65,129.09,135.15,135.68,166.77,169.25,173.08
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banxiaxiaoyu: ½ð±Ò+13, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-05-15 20:12:48
1 .     aspergillamide A (trans)
C28H34N4O3     ÏàËÆ¶È:69.2%
Tetrahedron          1998          54          13459-13466
Aspergillamides A and B: Modified cytotoxic tripeptides produced by a marine fungus of the genus Aspergillus
Steven G. Toske, Paul R. Jensen, Christopher A. Kauffman, William Fenical
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     JBIR-81
    ÏàËÆ¶È:68%
The Journal of Antibiotics          2010          63          389-391
Isolation of two new terpeptin analogs¡ªJBIR-81 and JBIR-82¡ªfrom a seaweed-derived fungus, Aspergillus sp. SpD081030G1f1
Miho Izumikawa, Junko Hashimoto, Motoki Takagi and Kazuo Shin-ya
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     aspergillamide B
C28H34N4P3     ÏàËÆ¶È:65.3%
Tetrahedron          1998          54          13459-13466
Aspergillamides A and B: Modified cytotoxic tripeptides produced by a marine fungus of the genus Aspergillus
Steven G. Toske, Paul R. Jensen, Christopher A. Kauffman, William Fenical
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     Methyl (S)-2-((R)-3-(1H-indol-3-yl)-2-(2-nitrobenzamido)propanamido)-4-methylpentanoate
C25H28N4O6     ÏàËÆ¶È:64%
Chinese Journal of Chemistry          2014          32          757−770
Bio-inspired Step-Economical, Redox-Economical and Protecting-Group-Free Enantioselective Total Syntheses of (−-Chaetominine and Analogues
Shi-Peng Luo, Qi-Long Peng, Chu-Pei Xu, Ai-E Wang, and Pei-Qiang Huang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     compound 6a
C29H31N5O3     ÏàËÆ¶È:60.7%
Chinese Chemical Letters          2012          24          462-465
Synthesis and cytotoxic activities of a series of novel N-methylbisindolylmaleimide amino acid ester conjugates
Ke Wang, Zheng Yan, Nan Wang, Zhan Zhu Liu
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     SF2809-I
C23H23N3O3     ÏàËÆ¶È:60%
The Journal of Antibiotics          2004          57          89-96
SF2809 Compounds, Novel Chymase Inhibitors from Dactylosporangium sp. 2. Structural Elucidation
MASATO TANI,KENZO HARIMAYA,YASUHIRO GYOBU,TORU SASAKI,OSAMI TAKENOUCHI,TAKASHI KAWAMURA,TAKASHI KAMIMURA and TOSHIAKI HARADA
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     Villocarine A
C22H26N2O3     ÏàËÆ¶È:60%
Bioorganic & Medicinal Chemistry          2011          19          4075-4079
New vasorelaxant indole alkaloids, villocarines A¨CD from Uncaria villosa
Hirotaka Matsuo, Ryuichi Okamoto, Kazumasa Zaima, Yusuke Hirasawa, Intan Safinar Ismail, Nordin Hj Lajis, Hiroshi Morita
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     5-[(4-ßÅßá»ù)-¶Ô¼×»ù±½¼×»ù]-2,2-ÑÇÎì»ù-1,4-¶þ‡fÍé-4,6-¶þͪ
C25H25NO4     ÏàËÆ¶È:60%
Chinese Journal of Organic Chemistry          2014          34          2487¨C2492
One-Pot Three-Component Synthesis of New ¦Â-Indole Derivatives in Gluconic Acid Aqueous Solution
Yan, Nan Xia, Jianhui Xiong, Yunkui Xiong, Bin Lin, Chunhua*, Liao, Weilin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     5-[(4-ßÅßá»ù)-ÁÚÂȱ½¼×»ù]-2,2-ÑÇÎì»ù-1,4-¶þ‡fÍé-4,6-¶þͪ
C24H22ClNO4     ÏàËÆ¶È:60%
Chinese Journal of Organic Chemistry          2014          34          2487¨C2492
One-Pot Three-Component Synthesis of New ¦Â-Indole Derivatives in Gluconic Acid Aqueous Solution
Yan, Nan Xia, Jianhui Xiong, Yunkui Xiong, Bin Lin, Chunhua*, Liao, Weilin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     (S)-3-Indol-1-(2-nitrobenzoyl)-3,4-dihydro-1H-benzo[1,4]diazepine-2,5-dione
C25H18N4O5     ÏàËÆ¶È:60%
Tetrahedron Letters          2015          56          1255−1258
Procedure¡ªeconomical enantioselective total syntheses of asperlicins C and E
Pei-Qiang Huang, Yu Wang, Shi-Peng Luo, Hui Geng, Yuan-Ping Ruan, Ai-E Wang
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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