| ²é¿´: 368 | »Ø¸´: 1 | |||
jinweiyangгæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖújyl-20µÄ½á¹¹ ÒÑÓÐ1È˲ÎÓë
|
|
13C NMR (101 MHz, CDCl3) ¦Ä 123.29,123.33,123.42,128.16,131.00,134.16,139.68,142.47,148.16 |
» ²ÂÄãϲ»¶
307·Ö²ÄÁÏרҵÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁÏר˶283Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
¼ÆËã»ú11408£¬286·ÖÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ14È˻ظ´
Ò»Ö¾Ô¸Äϲý´óѧ£¬085600£¬344·ÖÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
¿¼Ñе÷¼ÁÉúѰÕÒµ¼Ê¦
ÒѾÓÐ3È˻ظ´
²ÄÁÏ0856 Ó¢Ò»Êý¶þ 323 Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
»¯Ñ§0703-Ò»Ö¾Ô¸211-338·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
¡¾ÇóÖú¡¿¹ØÓÚPWSCF½á¹¹ÓÅ»¯Ð§Âʵ͵ÄÎÊÌâ
ÒѾÓÐ12È˻ظ´
ÇóÖú̼ËáÃ̵ľ§Ìå½á¹¹Îļþ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö¾§ÌåµÄÍØÆË½á¹¹¼°ÍØÆË·ÖÎö
ÒѾÓÐ8È˻ظ´
ÇóÖúSAPO-34¾§Ìå½á¹¹Í¼£¨ÒªÇò¹÷Ä£Ð͵ģ©
ÒѾÓÐ5È˻ظ´
ÖØ½ðÇóÖú ´Ë½á¹¹µÄά¶û˹Âõ¶û£¹þ¿Ë·´Ó¦
ÒѾÓÐ3È˻ظ´
[ÇóÖú]ÓйØPEIµÄ½á¹¹Ê½
ÒѾÓÐ5È˻ظ´
[ÇóÖú]¹ØÓÚ¶àëĵĽṹ·ÖÎö
ÒѾÓÐ4È˻ظ´
ÇóFe3O4, Fe2O3 and FeTiO3¾§Ìå½á¹¹
ÒѾÓÐ12È˻ظ´
ÇóÖúmPEG-DSPEµÄ½á¹¹Ê½
ÒѾÓÐ5È˻ظ´
ÇóÖúb-¹ÈçÞ´¼µÄ½á¹¹Ê½
ÒѾÓÐ4È˻ظ´
ÇóÖú¹¦ÄܲÄÁÏÓë½á¹¹²ÄÁϵĵÄ׼ȷ¶¨ÒåÓë·ÖÀà
ÒѾÓÐ3È˻ظ´
ÇóÖúÑó»±ÌǵĽṹʽ
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿¹ØÓÚÅäºÏÎïµÄ½á¹¹¡¢»·¨
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú£ºÇëÎÊethyldiaminocarbodiimide(EDC)µÄ½á¹¹
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿PMBµÄ½á¹¹Ê½ÊÇʲô£¿
ÒѾÓÐ3È˻ظ´
¡¾ÇóÖú¡¿Çå³þµÄµ°°×Öʶþ¼¶½á¹¹Í¼
ÒѾÓÐ6È˻ظ´
¡¾ÇóÖú¡¿ÇëÎʵ¥¾§½á¹¹×Ô¶¯ÐýתµÄÈí¼þ
ÒѾÓÐ6È˻ظ´
ÇóÖú½âÎö¾§Ìå½á¹¹µÄһЩÊý¾Ýº¬Òå
ÒѾÓÐ2È˻ظ´
¡¾ÇóÖú¡¿ÈçºÎ¸ù¾Ý½á¹¹Ê½ÕÒÌìÈ»²úÎïµÄÀàËÆ½á¹¹
ÒѾÓÐ17È˻ظ´
¡¾ÇóÖú/½»Á÷¡¿²ËÄñÇóÖú£¬ÈçºÎÓɵ°°×ÖʵÄÒ»¼¶½á¹¹µÃµ½Èý¼¶½á¹¹£¿
ÒѾÓÐ12È˻ظ´
¡¾ÇóÖú¡¿°±»ùËáÐòÁÐÈýά½á¹¹µÄ»ñµÃ
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿ÇóÖúÒ»¸öÒ©ÎïµÄ¾§Ìå½á¹¹Êý¾Ý£¡
ÒѾÓÐ15È˻ظ´
¡¾ÇóÖú¡¿½á¹¹Ê½µÄÃüÃû
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿¹ØÓÚÅжÏÕý·´¼â¾§Ê¯½á¹¹µÄÎÊÌâ
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿CastepÖнṹÓÅ»¯µÄÎÊÌâ
ÒѾÓÐ11È˻ظ´
¡¾ÇóÖú¡¿Çó¶àÌǵĸ߼¶½á¹¹Í¼
ÒѾÓÐ16È˻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
jinweiyang: ½ð±Ò+8, ¡ïÓаïÖú 2015-02-05 10:44:56
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
jinweiyang: ½ð±Ò+8, ¡ïÓаïÖú 2015-02-05 10:44:56
|
1 . ÐØÏÙà×ठÏàËÆ¶È:66.6% Chinese Journal of Marine Drugs 2011 30(5) 12-17 Studies on the chemical constituents of sponge Haliclona cymaeformis from the South China Sea WU Xu-dong,MEI Wen-li,SHAO Chang-lun,Nicole J.de Voogd,WANG Hu,WANG Chang-yun,DAI Hao-fu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 1H-indole-3-carboxylic acid ÏàËÆ¶È:66.6% Biochemical Systematics and Ecology 2012 43 210-213 Monoindole alkaloids from a marine sponge Mycale fibrexilis Ru-Ping Wang, Hou-Wen Lin, Ling-Zhi Li, Pin-Yi Gao, Ying Xu, Shao-Jiang Song Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 4-quinolinesulfonyl chloride ÏàËÆ¶È:66.6% Heterocycles 2007 71 1975-1990 From Haloquinolines and Halopyridines to Quinoline-and Pyridinesulfonyl Chlorides and Sulfonamides Andrzej Maslankiewicz, Krzysztof Marciniec, Maciej Pawlowski, and Pawel Zajdel Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . [Au(3ppy)Cl3] ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2009 47 658-665 1H, 13C and 15N nuclear magnetic resonance coordination shifts in Au(III), Pd(II) and Pt(II) chloride complexes with phenylpyridines (pages 658¨C665) Leszek Pazderski, Jarom¨ªr Toušek, Jerzy Sitkowski, Lech Kozerski and Edward Szłyk Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . N-(4-Nitrophenyl)phthalimide ÏàËÆ¶È:66.6% Archives of Pharmacal Research 2007 30 1501-1506 Synthesis of N-phenylphthalimide Derivatives as ¦Á-Glucosidase Inhibitors Wanchai Pluempanupat, Sirichai Adisakwattana, Sirintorn Yibchok-Anun and Warinthorn Chavasiri Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 4-Fluoroisoquinoline-5-sulfonyl chloride hydrochloride ÏàËÆ¶È:66.6% Heterocycles 2011 83 1771-1781 A Practical Synthesis of Novel Rho-Kinase Inhibitor, (S)-4-Fluoro-5-(2-methyl-1,4-diazepan-1-ylsulfonyl)isoquinoline Noriaki Gomi, Tadaaki Ohgiya, Kimiyuki Shibuya,* Jyunji Katsuyama, Masayuki Masumoto, and Hitoshi Sakai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (E)-Ethyl 3-(4-nitrophenyl)acrylate ÏàËÆ¶È:66.6% Tetrahedron 2012 68 1466-1474 Palladium-catalyzed double arylations of terminal olefins in acetic acid Daichao Xu, Chunxin Lu, Wanzhi Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-Phenyl-2-pyridinecarbonitrile C12H12N2 ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2012 595-603 Synthesis of Biaryls through a One-Pot Tandem Borylation/Suzuki¨CMiyaura Cross-Coupling Reaction Catalyzed by a Palladacycle Lianhui Wang, Xiuling Cui, Jingya Li, Yusheng Wu, Zhiwu Zhu and Yangjie Wu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 4,4'-bis-[3-(4-nitrobenzyl)-1H-imidazolium-1-yl]biphenyl dibromide C32H26N6O4 ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2011 19 6525-6542 The anti-malarial activity of bivalent imidazolium salts Jason Z. Vlahakis, Simona Mitu, Gheorghe Roman, E. Patricia Rodriguez, Ian E. Crandall, Walter A. Szarek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-nitro-N-pyrimidin-2-ylbenzenesulfonamide C10H9N4O4S ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 2009 17 7449-7456 In vivo and in vitro anti-leishmanial activities of 4-nitro-N-pyrimidin- and N-pyrazin-2-ylbenzenesulfonamides, and N2-(4-nitrophenyl)-N1-propylglycinamide M. Auxiliadora Dea-Ayuela, Encarna Castillo, Marta Gonzalez-Alvarez, Celeste Vega, Miriam Rol¨®n, Francisco Bol¨¢s-Fern¨¢ndez, Joaqu¨ªn Borr¨¢s, M. Eugenia Gonz¨¢lez-Rosende Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 5-(3-nitrophenyl)-3-oxy-1H-1,2,3-triazole-4-carboxylic acid C9H6N4O5 ÏàËÆ¶È:66.6% Russian Journal of Organic Chemistry 2005 41 591-598 3-Oxy-5-phenyl-1H-1,2,3-triazole-4-carboxylic Acid. Synthesis, Structure, and Properties O. V. Shtabova, S. D. Shaposhnikov, S. F. Mel¡¯nikova, I. V. Tselinskii and Ch. Nather, et al. Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . (E)-ethyl-3-(4-nitrophenyl)acrylate ÏàËÆ¶È:66.6% Tetrahedron 2012 68 6498-6503 Nucleophilic carbene-catalyzed redox-esterification reaction of ¦Á-halo-¦Á,¦Â-unsaturated aldehyde Xiang-Bo Wang, Xiao-Lei Zou, Guang-Fen Du, Zhi-Yong Liu, Bin Dai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 2a C13H10Br2S ÏàËÆ¶È:66.6% Tetrahedron 2013 69 5981-5988 Design and construction of supramolecular polysulfurated metallodendrimers with various shapes and sizes via coordination-driven self-assembly Nai-Wei Wu, Quan-Jie Li, Jing Zhang, Jiuming He, Jiang-Kun Ou-Yang, Hongwei Tan, Zeper Abliz, Hai-Bo Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-(1H-Imidazol-1-yl)pyridine ÏàËÆ¶È:66.6% Tetrahedron 2013 69 7279-7284 Ligand-free Cu2O-catalyzed cross coupling of nitrogen heterocycles with iodopyridines Original Research Article Yong-Chua Teo, Fui-Fong Yong, Shirlyn Sim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . N4,N4,N4',N4'-tetraphenyl-[1,1'-biphenyl]-4,4'-diamine C36H28N2 ÏàËÆ¶È:66.6% Tetrahedron 2014 70 4754-4759 Effects of solvent and base on the palladium-catalyzed amination: PdCl2(Ph3P)2/Ph3P-catalyzed selective arylation of primary anilines with aryl bromides Liangzhen Cai, Xuanying Qian, Wenjing Song, Taoping Liu, Xiaochun Tao, Wanfang Li, Xiaomin Xie Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . ¦Á-aryl-N-phenyl nitrone (p-Br) ÏàËÆ¶È:66.6% Organic Magnetic Resonance 1984 22 592-596 Investigation of substituent effects on the 1H and 13C NMR spectra of (Z)-N-(arylmethylene)-arylamine N-oxides (,N-diaryl nitrones) N. Arumugam, P. Manisankar, S. Sivasubramanian and D. A. Wilson Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 1,1-Difluoro-6-nitro-1H-indene C9H5F2NO2 ÏàËÆ¶È:66.6% Synthesis 2014 46 613-620 An Efficient and Convenient Protocol for the Synthesis of 1,1-Difluoro-6-nitro-2,3-dihydro-1H-indene Derivatives Zhang, Dongfeng; Li, Peng; Lin, Ziyun; Huang, Haihong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 2b ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 1989 27 611-615 Quantitative evaluation of electronic effects of the 1-tetrazolyl group from 1H and 13C NMR data for substituted 1-phenyltetrazoles Vladimir P. Karavai, Pavel N. Gaponik and Oleg A. Ivashkevich Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-02-04 16:04:56














»Ø¸´´ËÂ¥