| ²é¿´: 198 | »Ø¸´: 1 | ||||
hulizhi½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú
|
| 24.3,29.7,78.8,101.4,104.4,106.7,108.4,114.8,115.8,119.8,134.5,135.3,147.7,148.1,162.2,162.8,194.5 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸211£¬»¯Ñ§Ñ§Ë¶£¬310·Ö£¬±¾¿ÆÖصãË«·Ç£¬Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ13È˻ظ´
²ÄÁÏÓ뻯¹¤×¨Ë¶306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ19È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ19È˻ظ´
»¯¹¤Ñ§Ë¶ 285Çóµ÷¼Á
ÒѾÓÐ22È˻ظ´
298Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
368»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
326Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´

wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hulizhi: ½ð±Ò+18, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-08-06 22:43:20
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hulizhi: ½ð±Ò+18, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-08-06 22:43:20
|
°´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½40¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 7-hydroxy-3',4'-methylene-flavan ÏàËÆ¶È:70.5% Natural Product Research and Development 2010 22 987-990 Chemical Constituents of Myristica argentea Warb. SHI Ji; ZHAO Qi-miao; JIA Tia-zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (¡À)-7,4'-dihydroxy-3'-methoxyflavan ÏàËÆ¶È:58.8% Phytochemistry 1996 43 1265-1269 Five flavans from Mariscus psilostachys Eliane Garo, Marc Maillard, S¨¢ndor Antus, Steven Mavi, Kurt Hostettmann Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . (28)-8,5'-dihydroxy-7,3',4'-trimethoxyflavan C18H20O6 ÏàËÆ¶È:55.5% Journal of Natural Products 1991 Vol 54 196 Plant Anticancer Agents, XLVIII. New Cytotoxic Flavonoids from Muntingia calabura Roots Norito Kaneda, John M. Pezzuto, D. Doel Soejarto, A. Douglas Kinghorn, Norman R. Farnsworth, Thawatchai Santisuk, Patoomratana Tuchinda, Jinda Udchachon, Vichai Reutrakul Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . erythro-1-(3,4-Methylenedioxyphenyl)-2-{4-[(E)-1-propenyl]phenoxy}propan-1-ol C19H20O4 ÏàËÆ¶È:52.9% Phytochemistry 1996 42 1167-1169 Neolignans and a sesquiterpene from Caryodaphnosis tonkinensis Nguyen Hoang Anh, Helmut Ripperger, Tran Van Sung, G¨¹nter Adam Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (¡À)-7,4'-Dihydroxy-3'-methoxyflavan ÏàËÆ¶È:52.9% Phytochemistry 1995 38 745-749 Flavonoids of dragon's blood from Dracaena cinnabari Mohamed Masaoud, Helmut Ripperger, Andrea Porzel, G¨¹nter Adam Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (-)-N-methylviguine ÏàËÆ¶È:52.9% Phytochemistry 1991 30 2071-2074 Alkaloids from Sarcocapnos saetabensis Olga Blanco, Luis Castedo, Diego Cortes, M. Carmen Villaverde Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (2S)-7,3'-dimethoxy-4'-hydroxyflavan ÏàËÆ¶È:52.9% Phytochemistry 1988 27 1835-1841 Flavonoid and other constituents of Bauhinia manca Hans Achenbach,Markus Stöcker,Manuel A. Constenla Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 5-(3,4-methylenedioxyphenyl]-2-styryl-5-trifluoromethyl-2-oxazoline C19H14F3NO3 ÏàËÆ¶È:52.9% Journal of Heterocyclic Chemistry 2000 37 343-348 Unusual behaviour of N-cinnamoyl-2-hydroxy-2-(trifluoromethyl)-arylethylamines in pictet-gams cyclization. Synthesis of 2-styryl-5-aryl-5-trifluoromethyl-2-oxazolines L¨¢Szl¨® Posz¨¢v¨¢cz and Gyula Simig Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2-(4-fluorostyryl)-5-(3,4-methylenedioxyphenyl)-5-trifluoromethyl-2-oxazoline C19H13F4NO3 ÏàËÆ¶È:52.9% Journal of Heterocyclic Chemistry 2000 37 343-348 Unusual behaviour of N-cinnamoyl-2-hydroxy-2-(trifluoromethyl)-arylethylamines in pictet-gams cyclization. Synthesis of 2-styryl-5-aryl-5-trifluoromethyl-2-oxazolines L¨¢Szl¨® Posz¨¢v¨¢cz and Gyula Simig Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . N-[3',4'-methylenedioxy-(E)-cinnamoyl]anthranilic acid C17H13NO5 ÏàËÆ¶È:52.9% Indian Journal of Chemistry 2007 46B 2074-2078 A simple two-step synthesis of avenanthramides,constituents of oats (Avena sativa L) Kamat,Shrivallabh P; Parab,Sulaksha J Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . Compound 4a ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry Letters 2005 15 3717-3719 Microwave-assisted synthesis of imidazoles: Reaction of p-toluenesulfonylmethyl isocyanide and polymer-bound imines Swapan K. Samanta, Irene Kylänlahti, Jari Yli-Kauhaluoma Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . ((7S)-8'-(4'-hydroxy-3'-methoxyphenyl)-7-hydroxypropyl)benzene-2,4-diol C16H18O5 ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry Letters 2011 21 6884-6887 Inhibitory effect on NO production of phenolic compounds from Myristica fragrans To Dao Cuong, Tran Manh Hung, MinKyun Na, Do Thi Ha, Jin Cheol Kim, Dongho Lee, SungWoo Ryoo, Jeong Hyung Lee, Jae Sue Choi, Byung Sun Min Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . combretol B C17H18O5 ÏàËÆ¶È:52.9% Planta Medica 2011 77 1841-1844 Five New Diarylpropan-1-ols from Combretum yunnanense Wang, Li-Qin; Wu, Ming-Mei; Liu, Jing-Ping; Li, Yan; Hua, Yan; Wang, Yuan-Yuan; Li, Xing-Yao; Chen, Ye-Gao; Wang, Ji-hua: Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-[(3-pyridinylmethylidene)amino]-2-methyl-6,7-meth-ylenedioxy-quinazolin-4(3H)-onequinazolin-4(3H)-one derivative C16H12N4O3 ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry 2009 17 6517-6525 Synthesis and analgesic profile of conformationally constrained N-acylhydrazone analogues: Discovery of novel N-arylideneamino quinazolin-4(3H)-one compounds derived from natural safrole Rodolfo C. Maia, Leandro L. Silva, Eduardo F. Mazzeu, Milla M. Fumian, Claudia M. de Rezende, Antonio C. Doriguetto, Rodrigo S. Corr¨ºa, Ana Luisa P. Miranda, Eliezer J. Barreiro, Carlos Alberto Manssour Fraga Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (¡À)-2-(1,3-benzodioxol-5-yl)-2,3,dihydro-4(1H)-quinolinone C16H13NO3 ÏàËÆ¶È:52.9% Journal of Heterocyclic Chemistry 2011 48 613-619 (¡À)-2-Aryl-2,3-dihydro-4(1H)-quinolinones by a tandem reduction¨CMichael addition reaction Richard A. Bunce and Baskar Nammalwar Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-08-06 21:58:23














»Ø¸´´ËÂ¥