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13C NMR (126 MHz, MeOD) ¦Ä 176.90, 135.18, 129.65£¬ 75.14, 74.39, 71.69, 36.95, 33.98, 32.15, 31.62, 29.27, 29.01, 28.88, 25.45, 24.85, 22.33, 13.01. |
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- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
2Â¥2015-03-14 17:21:02
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3Â¥2015-03-14 17:36:41
hydros
½ð³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 613 (²©Ê¿)
- ½ð±Ò: 1073.3
- É¢½ð: 1218
- ºì»¨: 65
- Ìû×Ó: 1889
- ÔÚÏß: 249.7Сʱ
- ³æºÅ: 3334230
- ×¢²á: 2014-07-22
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
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³ÂÏþ´í: ½ð±Ò+10, ¡ïÓаïÖú 2015-03-14 18:31:10
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1 . 9,10,13-trihydroxy-(E)-11-octadecenoic acid C18H32O5 ÏàËÆ¶È:94.4% Natural Product Research and Development 1996 8(4) 28-32 SYNTHESIS OF NATURAL INSECTICIDE p-PHELLANDRENE Lu Kui; Liu Yanqi; Zhao Yingjie; Lu Chunming; Zhang Xiaolin; Jiang Yongjia Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Pinellic acid (9S,12S,13S-trihydroxy-10(E)-octadecenoicacid) ÏàËÆ¶È:94.4% Phytotherapy Research 2013 27 1376-1380 Inhibition of Prostaglandin D2 Production by Trihydroxy Fatty Acids Isolated from Ulmus davidiana var. japonica Hyun Gyu Choi, Yu Mi Park, Yue Lu, Hyeun Wook Chang, MinKyun Na and Seung Ho Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . methyl 11,12,15-trihydroxy-13(14)-octadecenoate C19H36O5 ÏàËÆ¶È:84.2% Indian Journal of Chemistry Section B 2003 42B 1782-1785 Terpenoid and lipid constituents from Artemisia annua Amit Tewari & Singh Bhakuni Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2015-03-14 17:39:30













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