| ²é¿´: 497 | »Ø¸´: 1 | ||
Ò©²Äͳæ (СÓÐÃûÆø)
|
[ÇóÖú]
awm-17 ̼Æ×Êý¾ÝÈçÏ ÒÑÓÐ1È˲ÎÓë
|
| 3C NMR (126 MHz, MeOD) ¦Ä 25.90,28.23,29.48,42.65,55.87,97.70,107.50,109.21,113.40,116.17,116.40,121.56,122.11,122.55,123.84,125.84,123.60,128.45,138.56,144.20,145.32,162.59,171.15 |
» ²ÂÄãϲ»¶
085501»úеר˶ 302·Ö ²»ÌôרҵÇóµ÷¼Á
ÒѾÓÐ3È˻ظ´
332£¬085601Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
292Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
314Çóµ÷¼Á
ÒѾÓÐ17È˻ظ´
Ò»Ö¾Ô¸Öйú¿ÆÑ§ÔºÉϺ£ÓлúËù£¬Óлú»¯Ñ§356·ÖÕÒµ÷¼Á
ÒѾÓÐ6È˻ظ´
291Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
¿¼ÑжþÂÖµ÷¼Á
ÒѾÓÐ4È˻ظ´
262Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
µ÷¼Á
ÒѾÓÐ17È˻ظ´
268·Ö085602»¯Ñ§¹¤³Ìµ÷¼Á
ÒѾÓÐ14È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
Óл¯ºÏÎï̼Æ×Êý¾ÝÈçÏ£¬Ç󻯺ÏÎï½á¹¹Ê½¡£ÇóÖúÇóÖú£¬¼±¼±£¬ÔÚÏߵȣ¬Ð»Ð»£¡½ð±Ò~~~~~~
ÒѾÓÐ6È˻ظ´
ÇóÔõÑùÓÃMestReNova 6.1¶Á³ö̼Æ×µÄÊý¾Ý
ÒѾÓÐ4È˻ظ´
½ñÌìÔÙÇóÒ»´Î΢Æ× ³ê½ð20 ллÁË °´Õչ涨¸ñʽÕûÀíºÃ̼Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ20%£©
ÒѾÓÐ3È˻ظ´
̼Æ×ÓÐ̼²»³ö·å£¬Êý¾ÝÄÜÓò»£¿
ÒѾÓÐ26È˻ظ´
MESTRENOVA 7 ½â̼Æ×£¬ÈçºÎÈÃÊä³öµÄÊý¾Ý±£ÁôһλСÊý£¨Ä¬ÈÏÊÇÁ½Î»£©£¿
ÒѾÓÐ12È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
¡¾ÇóÖú¡¿Çë³æÓÑÃǰï°ï½âÒ»ÏÂÕâ¸ö»¯ºÏÎï°¡£¬ÓÐÇâÆ×£¬Ì¼Æ×ºÍÖÊÆ×Êý¾Ý
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿Ì¼Æ×ÖÐȱÉÙÒÔôÊ»ù̼Êý¾Ý
ÒѾÓÐ12È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ò©²Ä: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-25 15:07:01
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
Ò©²Ä: ½ð±Ò+15, ¡ï¡ï¡ïºÜÓаïÖú 2015-03-25 15:07:01
|
²éѯ½á¹û£º¹²²éµ½146¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . trigonostemon F C20H16N2O3 ÏàËÆ¶È:73.9% Journal of Natural Products 2010 73 40-44 Constituents of Trigonostemon chinensis Qin Zhu, Chun-Ping Tang, Chang-Qiang Ke, Xi-Qiang Li, Jin Liu, Li-She Gan, Hans-Christoph Weiss, Ernst-Rudolf Gesing and Yang Ye Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 8d C30H24N3O6 ÏàËÆ¶È:60.8% Journal of Asian Natural products Research 2010 12 36-42 Synthesis and antitumor activity of bisindolylmaleimide and amino acid ester conjugates Ke Wang; Xiang-Yan Li; Xiao-Guang Chen; Zhan-Zhu Liu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 5 ÏàËÆ¶È:60.8% Magnetic Resonance in Chemistry 1992 30 905-908 Two-dimensional NMR analysis of selected photochromic spiroindolinonaphthoxazines V. Malatesta, P. Allegrini, C. Neri and L. Lanzini Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . oblongifoliagarcinine B C22H24O3 ÏàËÆ¶È:56.5% Helvetica Chimica Acta 2008 Vol. 91 938 New Biphenyl Constituents from Garcinia oblongifolia Xu Wu, Chang-Qiang Ke, Yi-Ping Yang, and Yang Ye Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . gisoflavone C21H20O6 ÏàËÆ¶È:56.5% Chemical & Pharmaceutical Bulletin 1989 37 3005-3009 Phenolic Constituents of Licorice. II. : Structures of Licopyranocoumarin, Licoarylcoumarin and Glisoflavone, and Inhibitory Effects of Licorice Phenolics on Xanthine Oxidase Tsutomu HATANO,Taeko YASUHARA,Toshiyuki FUKUDA,Tadataka NORO and Takuo OKUDA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . glioclatine C23H21N4O2S2 ÏàËÆ¶È:56.5% Chinese Chemical Letters 2006 17 922-924 A New Epidithiodioxopiperazine Metabolite Isolated from Gliocladium roseum YMF1.00133 Jin Yan DONG, Wei ZHOU, Lei LI, Guo Hong LI, Ya Jun LIU, Ke Qing ZHANG Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 4-2-(tert-butoxycarbonylamino)-3-(1H)indole-3-yl]propionyloxy-2(3H)-benzoxazolone ÏàËÆ¶È:56.5% Chinese Chemical Letters 2010 21 63-66 Synthesis and activities of new 4-hydroxybenzoxazolone derivatives Li Tang; Shu Rong Ban; Xiu E.Feng; Wen Han Lin; Qing Shan Li Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 5 ÏàËÆ¶È:56.5% Zeitschrift f¨¹r Naturforschung B 2007 62 314-322 Boryl-substituted Zirconocene Dichloride Complexes as Catalyst Precursors for Homogeneous Ethylene Polymerization A. Kestel-Jakob and H. G. Alt Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . N-(4-Methoxybenzenesulfonyl)-1-methyl-3-pentylfuro[3,4-b]indole C22H25NO4S ÏàËÆ¶È:56.5% Tetrahedron 2012 68 356-362 A convenient access to 1,3-disubstituted furo[3,4-b]indoles by acid ion-exchange resin-catalyzed furan formation Joan Basset, Manel Romero, Thaïs Serra, M. Dolors Pujol Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 3-Hexyl-N-(4-methoxybenzenesulfonyl)-1-methylfuro[3,4-b]indole C24H27NO4S ÏàËÆ¶È:56.5% Tetrahedron 2012 68 356-362 A convenient access to 1,3-disubstituted furo[3,4-b]indoles by acid ion-exchange resin-catalyzed furan formation Joan Basset, Manel Romero, Thaïs Serra, M. Dolors Pujol Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . javaberine A C24H23NO6 ÏàËÆ¶È:56.5% Heterocycles 2001 55 2043-2050 Javaberine A, New TNF-¦Á and Nitric Oxide Production Inhibitor, from the Roots of Talinum paniculatum Hiroshi Shimoda, Norihisa Nishida, Kiyofumi Ninomiya, Hisashi Matsuda, and Masayuki Yoshikawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 6-[2-(3,4-dihydroxyphenyl)ethylamino]-11H-indolo[3,2-c]quinoline hydrochloride C23H19N3O2 ÏàËÆ¶È:56.5% Bioorganic & Medicinal Chemistry 2010 18 1948-1957 Synthesis and antiproliferative evaluation of certain indolo[3, 2-c]quinoline derivatives Chih-Ming Lu, Yeh-Long Chen, Hui-Ling Chen, Chyi-An Chen, Pei-Jung Lu, Chia-Ning Yang, Cherng-Chyi Tzeng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 6,7,8,9-tetrahydrobenzo[c]azepino[1,2,3-lm]carbazole C20H17N ÏàËÆ¶È:56.5% European Journal of Organic Chemistry 2011 5905-5910 One-Pot Synthesis of Fused Benzo[c]carbazoles by Photochemical Intramolecular Annulation of 3-Acyl-2-haloindoles with Tethered Styrenes Shen-Ci Lu, Shi-Chao Wei, Wei-Xia Wang, Wei Zhang and Zhi-Feng Tu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . (9-methyl-9H-carbazole-3,6-diyl)bis((5-methylbenzofuran-2-yl)methanone) C33H23NO4 ÏàËÆ¶È:56.5% Heterocycles 2012 85 421-429 PEG-400-Promoted and Ultrasound Assisted Rap-Stoermer Reaction for Efficient Synthesis of Benzofuran-2-yl(carbazolyl)methanone Derivatives Yang Li, Yan Yan, and Wentao Gao Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 3-allyl-11-phenyl-2,3,6,11-tetrahydro-2,6-methano[1,3]thiazocino[8,7-b]indole-5-carbonitrile (major) ÏàËÆ¶È:56.5% Tetrahedron 2012 68 9685-9693 Pyridinium salts¡ªversatile reagents for the regioselective synthesis of functionalized thiazocino[2,3-b]indoles by tandem dinucleophilic reactions of thiooxindoles Mostafa Kiamehr, Firouz Matloubi Moghaddam, Pavel V. Gormay, Volodymyr Semeniuchenko, Alexander Villinger, Peter Langer, Viktor O. Iaroshenko Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . N-(3-fluoro-4-(thieno[2,3-d]pyrimidin-4-yloxy)phenyl)-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxamide C24H14F2N4O3S ÏàËÆ¶È:56.5% Bioorganic & Medicinal Chemistry 2011 19 3906-3918 Discovery of novel c-Met kinase inhibitors bearing a thieno[2,3-d]pyrimidine or furo[2,3-d]pyrimidine scaffold Ailing Zhao, Xin Gao, Yuanxiang Wang, Jing Ai, Ying Wang, Yi Chen, Meiyu Geng, Ao Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . Nortoprentin C C19H13N4Br ÏàËÆ¶È:56.5% The Journal of Organic Chemistry 1991 56 4304-4307 Nortopsentins A, B, and C. Cytotoxic and antifungal imidazolediylbis[indoles] from the sponge Spongosorites ruetzleri Shinichi Sakemi, Hao H. Sun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . N-(pyridin-4-ylmethylene)-4-(2,2,2-trifluoroethoxy)benzenamine C28H31F3N2O4 ÏàËÆ¶È:56.5% Monatshefte f¨¹r Chemie 2014 145 71−77 Synthesis and mesomorphic properties of new fluorinated hydrogen-bonded supramolecular liquid crystals Zhilian Liu, Jianzhi Han, Jian Zhang, Zhenning Yu, Tengfei Li, Shuxiang Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . N-(pyridin-4-ylmethylene)-4-(2,2,2-trifluoroethoxy)benzenamine C29H33F3N2O4 ÏàËÆ¶È:56.5% Monatshefte f¨¹r Chemie 2014 145 71−77 Synthesis and mesomorphic properties of new fluorinated hydrogen-bonded supramolecular liquid crystals Zhilian Liu, Jianzhi Han, Jian Zhang, Zhenning Yu, Tengfei Li, Shuxiang Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 9 C27H21N3O4 ÏàËÆ¶È:55.5% The Journal of Antibiotics 1996 49 519-526 Further Minor Metabolites of Staurosporine Produced by a Streptomyces longisporoflavm Strain YANG CAI, ANDREAS FREDENHAGEN, PAUL HUG, THOMAS MEYER, HEINRICH H. PETER Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . 4-(4-chlorophenyl)-8-methoxy-2-pentyloxy-5,6-dihydro-benzo[h]quinoline-3-carbonitrile C26H25ClN2O2 ÏàËÆ¶È:54.1% Journal of Heterocyclic Chemistry 2007 44 1525-1528 A novel synthesis of benzo[h]quinolines and study of their fluorescence properties Madhukar N. Jachak,Dhananjay B. Kendre,A. B. Avhale,Raghunath B. Toche and Ram W. Sabnis Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-03-25 07:42:11













»Ø¸´´ËÂ¥