| ²é¿´: 312 | »Ø¸´: 1 | ||
banxiaxiaoyuгæ (³õÈëÎÄ̳)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| 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 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸»ª¶«Ê¦·¶ÉúÎïѧ326·Ö£¬Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
071000ÉúÎïѧµ÷¼ÁÇóÖú
ÒѾÓÐ11È˻ظ´
»¯Ñ§¹¤³ÌÓë¼¼Êõ324µ÷¼Á
ÒѾÓÐ16È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
282£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ19È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
ÖпÆÔº×Ü·Ö315Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á ²ÄÁÏÓ빤³Ì 324·Ö ר˶
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸¿ó´ó£¬²ÄÁϹ¤³Ìר˶314·Ö£¬0856¿Éµ÷¶¼¿ÉÒÔ
ÒѾÓÐ12È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48426.9
- ºì»¨: 52
- Ìû×Ó: 6748
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
banxiaxiaoyu: ½ð±Ò+13, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-05-15 20:12:48
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
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 ̼Æ×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 ̼Æ×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 ̼Æ×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 AnaloguesShi-Peng Luo, Qi-Long Peng, Chu-Pei Xu, Ai-E Wang, and Pei-Qiang Huang Structure 13C NMR Structure & 13C NMR ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×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 ̼Æ×Ä£Äâͼ |

2Â¥2015-05-15 20:00:08













»Ø¸´´ËÂ¥
-Chaetominine and Analogues