| ²é¿´: 319 | »Ø¸´: 1 | |||
liuxiaosaľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖúFA2 ÒÑÓÐ1È˲ÎÓë
|
| 29.7, 55.3, 55.4, 55.8, 55.9, 88.2, 88.3, 100.3, 100.4, 114.2, 114.2, 116.2, 116.3, 127.8, 128.7, 135.2, 158.8, 160.5, 163.8, 170.9 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
353Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁϹ¤³Ì302·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çó
ÒѾÓÐ3È˻ظ´
²ÄÁÏÓ뻯¹¤363ÇóÍÆ¼ö
ÒѾÓÐ4È˻ظ´
085602µ÷¼Á ³õÊÔ×Ü·Ö335
ÒѾÓÐ11È˻ظ´
081700ѧ˶£¬323·Ö£¬Ò»Ö¾Ô¸Öйúº£Ñó´óѧÇóµ÷¼ÁѧУ
ÒѾÓÐ12È˻ظ´
085410È˹¤ÖÇÄÜ ³õÊÔ316·Ö Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
²ÄÁÏ»¯¹¤306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ11È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»°ïÖú¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»~
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú,лл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл¸÷λ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл´ó¼Ò
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¡¼±¼±¼±£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú1¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×²éѯ½âÆ×
ÒѾÓÐ5È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- 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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
liuxiaosa: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-01-29 18:25:09
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
liuxiaosa: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-01-29 18:25:09
|
1 . yangonin ÏàËÆ¶È:70% Phytochemistry 2002 59 429-433 Kavalactones from Piper methysticum, and their 13C NMR spectroscopic analyses H. Ranjith W. Dharmaratne, N.P. Dhammika Nanayakkara, Ikhlas A. Khan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 2-methoxy-6-[2-(4-methoxyphenyl)ethenyl]pyran-4-one C15H14O4 ÏàËÆ¶È:65% Phytochemistry 1997 45 701-703 Antifungal stress compounds from Vicia cracca Mustafa M. Saleh, Karl-Werner Glombitza Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . Yangonin ÏàËÆ¶È:65% Phytomedicine 2003 10 309-317 Isolation and synthesis of TNF-a release inhibitors from Fijian kawa (Piper methysticum) T. Hashimoto1, M. Suganuma2, H. Fujiki1,2, M. Yamada3, T. Kohno3, and Y. Asakawa1 Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . N1,N3-Bis((Z)-2-amino-1,2-dicyanovinyl)-2-(1-(tert-butylamino)-3,3-dicyano-2-(4-methoxyphenyl)propylidene)malonamide C27H25N11O3 ÏàËÆ¶È:57.1% Tetrahedron 2014 70 9512-9521 One-pot synthesis of 1,2,4,5-tetrahydro-2,4-dioxobenzo[1,4]diazepine and malonamide derivatives using multi-component reactions Abbas Rahmati, Samaneh Ahmadi, Mahdi Ahmadi-Varzaneh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 4-Methoxy-6-(11,12-methylenedioxy-10,14-dimethoxystyryl)-2-pyrone ÏàËÆ¶È:55% Biochemical Systematics and Ecology 2004 32 603-606 A new styryl-2-pyrone derivative from Polygala sabulosa (Polygalaceae) Moacir Geraldo Pizzolatti, Anildo Cunha Jr., Wagner Souto Pereira, Franco Delle Monache Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 7,8-Epoxyyangonin ÏàËÆ¶È:55% Phytomedicine 2003 10 309-317 Isolation and synthesis of TNF-a release inhibitors from Fijian kawa (Piper methysticum) T. Hashimoto1, M. Suganuma2, H. Fujiki1,2, M. Yamada3, T. Kohno3, and Y. Asakawa1 Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 15 ÏàËÆ¶È:55% Phytochemistry 1985 24 163-169 Constituents of Papaver bracteatum: O-methyl-¦Á-thebaol and 10-n-nonacosanol. Lanthanide-induced chemical shifts in 1H NMR and 13C NMR Hubert G. Theuns, Richard H.A.M. Janssen, Hubertus W.A. Biessels, Cornelis A. Salemink Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 7,4'-dimethoxyisoflavone ÏàËÆ¶È:55% Chinese Traditional and Herbal Drugs 2005 36 1469-1471 ×ÏË뻱ϸ°û¶¾»îÐÔ²¿Î»»¯Ñ§³É·ÖÑо¿ ½ªãü,°×ÀöƼ,¿µÍ¢¹ú Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 2a C21H23BrO7 ÏàËÆ¶È:55% Tetrahedron Letters 2001 42 8907-8909 An environmentally benign synthesis of aurones and flavones from 2'-acetoxychalcones using n-tetrabutylammonium tribromide Gopal Bose, Ejabul Mondal, Abu T Khan, Manob J Bordoloi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-[(dimethylamino)methyl]-5-methoxy-N-(4-methoxyphenyl)-N-methyl-1H-indole-2-carboxamide ÏàËÆ¶È:55% Bioorganic & Medicinal Chemistry 2009 17 4583-4594 Synthesis and pharmacological evaluation of 1,2,3,4-tetrahydropyrazino[1,2-a]indole and 2-[(phenylmethylamino)methyl]-1H-indole analogues as novel melatoninergic ligands Christian Markl, Mohamed I. Attia, Justin Julius, Shalini Sethi, Paula A. Witt-Enderby, Darius P. Zlotos Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . (E)-6-(2,4-dimethoxystyryl)-4-methoxy-2H-pyran-2-one C16H16O5 ÏàËÆ¶È:55% European Journal of Organic Chemistry 2012 3607-3616 Heck¨CMatsuda Arylation as a Strategy to Access Kavalactones Isolated from Polygala sabulosa, Piper methysticum, and Analogues Cristian Soldi, Ang¨¦lica V. Moro, Moacir G. Pizzolatti and Carlos R. D. Correia Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 18 ÏàËÆ¶È:55% Organic Magnetic Resonance 1982 20 166-169 Carbon-13 NMR studies. 96¡ªcarbon-13 spectra of several polyhydroxylated 9,10-dihydrophenanthrene and phenanthrene derivatives Albert Stoessl and J. B. Stothers Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 4',5,7-Trihydroxy-8-(cyclohexylamino)-2-phenyl-4H-chromen-4-one ÏàËÆ¶È:55% Molecules 2012 17 14748-14764 Nitrogen-Containing Apigenin Analogs: Preparation and Biological Activity Rui Liu, Bin Zhao, Dong-En Wang, Tianyu Yao, Long Pang, Qin Tu, Saeed Mahmoud Ahmed, Jian-Jun Liu and Jinyi Wang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 7,4'-dimethoxyisoflavone ÏàËÆ¶È:55% Journal of Chinese Medicinal Materials 2005 28 19-20 ×ÏËë»±¹ûʵ»¯Ñ§³É·Ö ½ªãü, °×ÀöƼ, ¿µÍ¢¹ú, Çú¾², ³ÂÓî Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 14-oxonaamidine G C24H23N5O5 ÏàËÆ¶È:55% Helvetica Chimica Acta 1995 78 1178-1184 Novel Naamidine-Type Alkaloids and Mixed-Ligand Zinc(II) Complexes from a Calcareous Sponge, Leucetta sp., of the Coral Sea Ines Mancini, Graziano Guella, C¨¦cile Debitus and Francesco Pietra Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . Methyl 4-(4-methoxyphenyl)-3-[2-(4-methoxyphenyl)ethynyl]isoquinolin-7-yl ether C26H21NO3 ÏàËÆ¶È:54.5% Tetrahedron 2012 68 8207-8215 Synthesis of 8-aryl substituted benzo[a]phenanthridine derivatives by consecutive three component tandem reaction and 6-endo carbocyclization Anil K. Mandadapu, Meena D. Dathi, Rajesh K. Arigela, Bijoy Kundu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-01-29 18:02:40














»Ø¸´´ËÂ¥