| ²é¿´: 402 | »Ø¸´: 1 | ||
bin85666666гæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý²éѯ ÒÑÓÐ1È˲ÎÓë
|
|
ÎҵϝºÏÎï̼Æ×Êý¾ÝÈçÏ£º 18.1,18.6,19.7,32.1,40.8,41.1,74.3,115.2,126.8,129.4,130.3,130.7,157.8 3Q! |
» ²ÂÄãϲ»¶
302·ÖÇóµ÷¼Á Ò»Ö¾Ô¸°²»Õ´óѧ085601
ÒѾÓÐ5È˻ظ´
²ÄÁÏÓ뻯¹¤371Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
313Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
²ÄÁϹ¤³Ì302·ÖÇóµ÷¼Á
ÒѾÓÐ5È˻ظ´
ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ4È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ8È˻ظ´
¸´ÊÔµ÷¼Á
ÒѾÓÐ6È˻ظ´
Çó
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
¼±Çó΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
¡¾·ÖÏí¡¿Ãâ·ÑµÄ20¸öÆ×ͼÊý¾Ý¿â
ÒѾÓÐ13È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
bin85666666: ½ð±Ò+20 2014-06-03 16:38:16
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
bin85666666: ½ð±Ò+20 2014-06-03 16:38:16
|
²éѯ½á¹û£º¹²²éµ½119¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . compound 8(E) C15H17N3O ÏàËÆ¶È:61.5% Journal of Heterocyclic Chemistry 2000 37 1089-1096 A series of diarylsubstituted oximes as potential substrate for new aldose reductase inhibitors Dietmar Rakowitz, Gottfried Heinisch, Peter Lukavsky, Sigrid Kiendler, Cornelia Trenkwalder, Daniela Barlocco, Giulio Rastelli and Luca Costantino Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . stachyline D C13H18O4 ÏàËÆ¶È:61.5% Journal of Natural Products 2011 74 21-25 Stachylines A−D from the Sponge-Derived Fungus Stachylidium sp. Celso Almeida, Natalja Part, Sarah Bouhired, Stefan Kehraus, and Gabriele M. König Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . isobutyl 2-diazo-3-oxo-5-phenylpentanoate ÏàËÆ¶È:60% Tetrahedron Letters 2004 45 2417-2419 Metalation of ¦Á-diazocarbonyl compounds using Grignard reagents. A convenient synthesis of ¦Á-diazo-¦Â-ketoesters and mixed esters of ¦Á-diazomalonate Erick Cuevas-Yañez, Joseph M. Muchowski, Raymundo Cruz-Almanza Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Compound 5 ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 1991 1 535-538 The enzymatic Baeyer-Villiger oxidation: synthesis of the C11¨CC16 subunit of ionomycin Michael J. Taschner, Quin-Zene Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . N-(2,2-dicyano-1-thioxoethyl)-N-[(4-methylphenyl)sulfonyl]pentanethioamide C16H17N3O2S3 ÏàËÆ¶È:57.1% Helvetica Chimica Acta 2013 96 2141-2146 Copper-Catalyzed Synthesis of 2H-Thiopyran Derivatives from Alkynes, Sulfonyl Azides, Carbon Disulfide, and Malononitrile Issa Yavari, Manijeh Nematpour and Ziba Tavakoli Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . atenolol ÏàËÆ¶È:57.1% Magnetic Resonance in Chemistry 2011 49 284-290 1H and 13C NMR characteristics of ¦Â-blockers Monika Agnieszka Zieli¨½ska-Pisklak, Dariusz Maciej Pisklak and Iwona Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (3Z,6E)-1-N-methyl-3-benzylidene-6-(2S-methyl-3-hydroxypropylidene)-piperazine-2,5-dione and (3Z,6E)-1-N-methyl-3-benzylidene-6-(2R-methyl-3-hydroxypropylidene)-piperazine-2,5-dione C16H18N2O3 ÏàËÆ¶È:57.1% Marine Drugs 2013 11 1035-1049 Communication: Diketopiperazine Derivatives from the Marine-Derived Actinomycete Streptomyces sp. FXJ7.328 Pei Wang, Lijun Xi, Peipei Liu, Yi Wang, Wei Wang, Ying Huang and Weiming Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . trichomanin C50H38O10 ÏàËÆ¶È:53.8% Chemistry & Biodiversity 2005 Vol. 2 139 Antuifungal Constituents from the chinese Moss Homalia trichomanoides Xiao-ning Wang,Wen-tao Yu,and Hong-xiang Lou Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . pregeijerene B C12H18 ÏàËÆ¶È:53.8% Phytochemistry 2003 105-108 A pregeijerene isomer from Juniperus erectopatens foliage Laurence G. Cool, Robert P. Adams Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (2S)-2-Amino-3-(2,4-dimethylphenyl) propan-1-ol hydrochloride ÏàËÆ¶È:53.8% Molecules 2004 9 405-426 Synthesis of Chiral Building Blocks for Use in Drug Discovery Sharon T. Marino, Danuta Stachurska-Buczek, Daniel A. Huggins, Beata M. Krywult, Craig S. Sheehan, Thao Nguyen, Neil Choi, Jack G. Parsons, Peter G. Griffiths, Ian W. James, Andrew M. Bray, Jonathan M. White and Rustum S. Boyce Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . N-(4'-Hydroxybiphenyl-3-yl)-2-(3-hydroxyphenyl)-N-methylacetamide ÏàËÆ¶È:53.8% Bioorganic & Medicinal Chemistry 2011 19 807-815 17¦Â-HSD2 inhibitors for the treatment of osteoporosis: Identification of a promising scaffold Marie Wetzel, Sandrine Marchais-Oberwinkler, Rolf W. Hartmann Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 1-{(4S)-4-Benzyl-4,5-dihydro-oxazol-2-yl}-(2S)-2-methylpropylamine C14H21N2O ÏàËÆ¶È:53.8% Canadian Journal of Chemistry 2007 85 85-95 Modular syntheses of oxazolinylamine ligands and characterization of group 10 metal complexes Christine A. Caputo, Florentino d.S. Carneiro, Michael C. Jennings, and Nathan D. Jones Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . O-benzyl-L-tyrosinol C16H19NO2 ÏàËÆ¶È:53.8% Canadian Journal of Chemistry 2011 89 88¨C91 Synthesis of a new chiral auxiliary¡ªNon-cross-linked polystyrene-supported oxazolidine-2-selone Xiping He, Jia Li, Cuifen Lu, Zuxin Chen, and Guichun Yang Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 16B ÏàËÆ¶È:53.8% Journal of Heterocyclic Chemistry 2006 43 723-729 A study on the ability of 2,5-dihydro-and 2,3,4,5-tetrahydro-1h-phosphole oxides,as well as 7-phosphanorbornene 7-oxide derivatives to undergo uv light-mediated fragmentation-related phosphinylation of methanol Gyöurgy Keglevich,J¨¢nos Kov¨¢cs,Helga Szelke and Tam¨¢s Köurtv¨¦alyesi Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-05-31 14:20:05














»Ø¸´´ËÂ¥