| ²é¿´: 482 | »Ø¸´: 1 | ||
ůÐÄ89ͳæ (СÓÐÃûÆø)
|
[ÇóÖú]
̼Æ×ÇóÖú£¬Ð»Ð» ÒÑÓÐ1È˲ÎÓë
|
|
ë®´ú±ûͪ´òÆ× 29.84,40.47,51.87,115.98,126.15,131.13,157.22,172.65,206.21 |
» ²ÂÄãϲ»¶
¿É¿¿ÏûÏ¢£¬8ÔÂ21ºÅ(Ã÷Ìì)·Å°ñ
ÒѾÓÐ3È˻ظ´
Ö»ÓÐÿÄêÕâÖÖʱºòÀ´¹ä¹äСľ³æ
ÒѾÓÐ20È˻ظ´
»¶Ó·¢À´filecodeµÄMz6ºóµÄ´úÂëÑéÖ¤Æä¹æÂÉ
ÒѾÓÐ125È˻ظ´
½ñÌì»ù½ð»á³ö½á¹ûÂð£¿20260819
ÒѾÓÐ15È˻ظ´
ʱ¼ä´Á±äÁË£¬ÄÜ¿´³öʲôÎÊÌ⣿
ÒѾÓÐ16È˻ظ´
filecode£¬4¸öjtjcÁË
ÒѾÓÐ13È˻ظ´
ΪʲôÓà¶î±¦µÄÄ껯ÀûÂÊÔ½À´Ô½µÍ£¿Ö÷ÒªÔÒòÓÐÄÄЩ£¿
ÒѾÓÐ5È˻ظ´
½ñÌì·Å°ñûϷÁ˰É
ÒѾÓÐ5È˻ظ´
½ñÌì·Å°ñÂð£¿
ÒѾÓÐ15È˻ظ´
filecode=ºóÃæµÚÒ»¸öÊÇ´óд×Öĸ
ÒѾÓÐ12È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Íò·Ö¸Ðл£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬¼±£¡~~лл
ÒѾÓÐ3È˻ظ´
·Ç³£¸Ðл£¡Î¢Æ×ÇóÖú
ÒѾÓÐ3È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð» £¨TE1-1£©
ÒѾÓÐ3È˻ظ´
Ò»°ã´ò̼Æ×»òÇâÆ×ÓÃʲôÈܼÁ
ÒѾÓÐ7È˻ظ´
ë®´ú±½µÄÇâÆ×ºÍ̼Æ×
ÒѾÓÐ9È˻ظ´
¹ØÓÚÈý·ú¼×»ù̼Æ×»¯Ñ§Î»ÒƵÄÎÊÌâ
ÒѾÓÐ3È˻ظ´
̼Æ×ÓÐ̼²»³ö·å£¬Êý¾ÝÄÜÓò»£¿
ÒѾÓÐ26È˻ظ´
̼Æ×Ò²ÓÐÁ½Öط壬ÈýÖØ·å£¬¶àÖØ·åô£¿²ËÄñ²»¶®£¬Çóµã²¦£¡
ÒѾÓÐ25È˻ظ´
NMR̼Æ×£¬Çë´ó¼ÒÌÖÂÛÒ»ÏÂÆ×ͼÖеķå
ÒѾÓÐ21È˻ظ´
ÇëÎÊÌìÈ»ÓлúµÄͬѧ£¬º¬µª»¯ºÏÎïºË´ÅµÄ̼13Æ×£¬»á³öÏÖÓÐЩ̼²»³ö·åµÄÇé¿öÂð£¿
ÒѾÓÐ14È˻ظ´
¡¾ÇóÖú¡¿·ÖÀëÌá´¿µÃµ½µÄ»¯ºÏÎï¼òµ¥ÇâÆ×ºÍ̼Æ×½âÎö
ÒѾÓÐ10È˻ظ´
[ÇóÖú]ÑùƷ̼Æ×Ò»¸öÎÊÌâ
ÒѾÓÐ7È˻ظ´
ÇóÖú~~´ÓºË´ÅÆ×£¨ÇâÆ×£¬Ì¼Æ×£©ÖУ¬ÔõôÄÜ¿´³öÊÇľÌÇ»¹Êǰ¢À²®ÌÇ£¿
ÒѾÓÐ6È˻ظ´
¹ØÓÚ»¯ºÏÎï̼Æ×»¯Ñ§Î»ÒƶԲ»ÉÏ£¬ÐèУÕýµÄÎÊÌâ¡£Çó¸ßÈ˽â´ð...
ÒѾÓÐ8È˻ظ´
¡¾ÇóÖú¡¿¹ØÓÚ̼Æ×Öп¨±ö̼µÄλÖÃ
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ë®´ø»¯ºÏÎï̼Æ× Çó½âÊÍ
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿Ì¼Æ×ÖÐȱÉÙÒÔôÊ»ù̼Êý¾Ý
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿Ì¼Æ×È¥ñîÎÊÌâ
ÒѾÓÐ10È˻ظ´
¡¾ÇóÖú¡¿ºË´ÅÇâÆ×»òÕß̼Æ×ÈçºÎ¿´º¬Á¿
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿´ò̼Æ×ºÍÇâÆ×£¬ÎÒµÄÑùÆ·¹»²»¹»°¡
ÒѾÓÐ10È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48941.7
- ºì»¨: 52
- Ìû×Ó: 6845
- ÔÚÏß: 546.6Сʱ
- 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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ůÐÄ89: ½ð±Ò+7, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-24 19:25:27
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ůÐÄ89: ½ð±Ò+7, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2015-03-24 19:25:27
|
1 . p-hydroxyphenylacetic acid methyl ester ÏàËÆ¶È:66.6% Chinese Pharmaceutical Journal 2009 44 490-492 Studies on Chemical Constituents in Forsythia suspensa (Thunb.) Vahl FENG Wei-sheng, LI Ke-ke, ZHENG Xiao-ke Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . methyl-2-(4-methoxymethoxy)phenyl acetate C11H14O4 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2010 18 3387-3402 Serotonin derivatives as a new class of non-ATP-competitive receptor tyrosine kinase inhibitors Anita B¨¹ttner, Thomas Cottin, Jing Xu, Lito Tzagkaroulaki, Athanassios Giannis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 4-hydroxyphenylacetic acid C8H8O3 ÏàËÆ¶È:66.6% Zeitschrift f¨¹r Naturforschung C 2011 66 31-34 Nematicidal Activities of 4-Hydroxyphenylacetic Acid and Oidiolactone D Produced by the Fungus Oidiodendron sp. K. Ohtani, S. Fujioka, T. Kawano, A. Shimada, and Y. Kimura Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . methyl(4-OH) phenylacetate ÏàËÆ¶È:66.6% Journal of Chinese Medicinal Materials 2012 35 1602-1604 Chemical Constituents from Pleione bulbocodioides YUAN Qiao-yu, LIU Xin-qiao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 2-(4-hydroxy)phenyl acetic acid methyl ester ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2013 21 7699-7708 Tyrosinase and Layer-by-Layer supported tyrosinases in the synthesis of lipophilic catechols with antiinfluenza activity Tiziana Bozzini, Giorgia Botta, Michela Delfino, Silvano Onofri, Raffaele Saladino, Donatella Amatore, Rossella Sgarbanti, Lucia Nencioni, Anna Teresa Palamara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . methyl p-hydroxybenzeneacetate ÏàËÆ¶È:66.6% Lishizhen Medicine and Materia Medica Research 2010 21 1127-1128 º£É߸ÉÌåµÄ»¯Ñ§³É·ÖÑо¿ À×Óð; ÐÜÁÁ; Íõϼ; Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 4-Methoxyphenylacetic acid ÏàËÆ¶È:66.6% European Journal of Plant Pathology 2012 134 239-247 Toxins from a symbiotic fungus, Leptographium qinlingensis associated with Dendroctonus armandi and their in vitro toxicities to Pinus armandi seedlings Xiao-Jun Li, Jin-Ming Gao, Hui Chen, An-Ling Zhang, Ming Tang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . methyl 4-hydroxybenzeneacetate ÏàËÆ¶È:66.6% Chinese Pharmaceutical Journal 2013 48 1815-1819 Chemical Constituents of the Aerial Parts of Emilia sonchifolia ( II) SHEN Shou-mao, ZHANG Jing, LI Guang-zhi, LIU Chun-ming, LU Hui, SI Jian-yong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl 2-(4-hydroxyphenyl)acetate C9H10O3 ÏàËÆ¶È:66.6% Acta Microbiologica Sinica 2012 52 1103-1112 Secondary metabolites of halotolerant fungus Penicillium chrysogenum HK14-01 from the Yellow River Delta area Peng Qu Peipei Liu Peng Fu Yi Wang Weiming Zhu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . methyl4-hydroxyphenylacetate ÏàËÆ¶È:66.6% Guangzhou Chemistry 1996 45-48 A Study on the chemical constituents of the marine sponge pachychalina sp. from south China sea Xiao Dingjun, Deng Songzhi, Wu Houming Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . methyl 5,5,5-trifluoro-4-(p-fluorophenylamino)pentanoate C12H13F4NO2 ÏàËÆ¶È:60% European Journal of Organic Chemistry 2010 1778-1786 Reductive Amination/Cyclization of ¦Ø-Trifluoromethyl Keto Esters to Trifluoromethylated ¦Ä-Amino Alcohols and Lactams Wen Wan, Jie Hou, Haizhen Jiang, Zongqian Yuan, Goubin Ma, Gang Zhao and Jian Hao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . methyl 3-(2-oxo-2H-benzo[1,4]oxazin-3-yl)propanoate C12H11NO4 ÏàËÆ¶È:58.3% Journal of Heterocyclic Chemistry 2013 50 413-416 Novel 3-(2-Oxo-2H-benzo[1,4]oxazin-3-yl)propanoates from Dimethyl-2-oxoglutarate and Test of Their Biological Activity Kamel Hachama, Mohamed Khodja, Saad Moulay, Hocine Boutoumi, Lothar Hennig and Dieter Sicker Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 5-[3-(aminocarbonyl)-4-hydroxybenzyl]-2-hydroxybenzamide ÏàËÆ¶È:55.5% Chinese Chemical Letters 2007 18 1213-1217 Zirconyl chloride promoted highly efficient solid phase synthesis of amide derivatives Cherkupally sanjeeva Reddy£¬Adki Nagaraj£¬Pochampally Jalapathi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (2S,3R,5R,6S)-2,3,5,6-tetrahydroxy-4-[2-[4-hydroxyphenyl)acetyl]oxycyclohexyl-2-(4-hydroxy-phenyl)-acetate C22H24O10 ÏàËÆ¶È:55.5% Phytochemistry 1999 51 991-994 Eudesmanolides and inositol derivatives from Taraxacum linearisquameum C. Zidorn, E.P. Ellmerer-Muller, H. Stuppner Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 2-hydroxy benzoic hydrazide C7H8N2O2 ÏàËÆ¶È:55.5% Indian Journal of Chemistry Section B 2010 49B 526-531 Development and assessment of green synthesis of hydrazides Ajoy Saha,Rajesh Kumar*,Rajendra Kumar & C Devakumar Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . p-hydroxyphenylacetic acid ÏàËÆ¶È:55.5% Chinese Traditional and Herbal Drugs 2010 41 700-703 ´©ÁúÊíÝ÷µØÉϲ¿·ÖµÄ»¯Ñ§³É·Ö(¢ò) ¬µ¤;Áõ½ðƽ;ÕÔéó׿;³Â˧;ÀîÆ½ÑÇ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 5-(4-Hydroxybenzyl)thiazolidine-2,4-dione ÏàËÆ¶È:55.5% Archives of Pharmacal Research 2004 27 1099-1105 Synthesis and biological activity of Benzoxazole containing thiazolidinedione derivatives Raok Jeon and SoYeon Park Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 5-(4-Hydroxybenzyl)thiazolidine-2,4-dione ÏàËÆ¶È:55.5% Archives of Pharmacal Research 2005 28 377-381 Synthesis of polymeric thiazolidinediones and L-ascorbic acid towards the development of insulin-sensitizer Sun Mi Lee and Raok Jeon Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-24 18:45:00









»Ø¸´´ËÂ¥