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libinoookľ³æ (ÕýʽдÊÖ)
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ÇóÖú΢Æ×Êý¾Ý12
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| 13C NMR (151 MHz, cdcl3) ¦Ä 158.77, 158.74, 149.62, 141.11, 134.59, 133.27, 128.92, 126.94, 123.46, 120.88, 120.75, 120.34, 116.70, 110.29, 108.07, 29.71, 19.73, 8.70. |
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libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-11-13 13:18:28
libinoook: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-11-13 13:18:28
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²éѯ½á¹û£º¹²²éµ½587¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . tanshinlactone C17H12O3 ÏàËÆ¶È:88.8% Chemical & Pharmaceutical Bulletin 1986 34 3166-3168 Tanshinlactone, a Novel Seco-abietanoid from Salvia miltiorrhiza HOU-WEI LUO,JIANG JI,MEI-YU WU,ZHONG-GEN YONG,MASATAKE NIWA and YOSHIMASA HIRATA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . Neo-tanshinlactone C17H12O3 ÏàËÆ¶È:88.8% Journal of Medicinal Chemistry 2004 47 5816-5819 Antitumor Agents. 239. Isolation, Structure Elucidation, Total Synthesis, and Anti-Breast Cancer Activity of Neo-tanshinlactone from Salvia miltiorrhiza Xihong Wang, Kenneth F. Bastow, Chang-Ming Sun, Yun-Lian Lin, Hsi-Jung Yu, Ming-Jaw Don, Tian-Shung Wu, Seikou Nakamura, and Kuo-Hsiung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . neo-tanshinlactone ÏàËÆ¶È:88.8% Heterocycles 2012 86 785-789 SYNTHESIS OF NEO-tANSHINLACTONE VIA THE PALLADIUM-MEDIATED INTRAMOLECULAR BIARYL COUPLING REACTION Hitoshi Abe,* Toshitaka Kawai, Yoshinori Komatsu, Mayu Kamimura, Yasuo Takeuchi, and Yoshikazu Horino Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . tanshinlactone ÏàËÆ¶È:88.8% Chinese Pharmaceutical Journal 2011 46 977-979 Study on Chemical Constituents of Salvia grand ifolia XIAO, Lei, WANG, Hong-qing, MA, Lin, CHEN, Ruo-yun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . tanshinlactone ÏàËÆ¶È:77.7% Natural Product Research and Development 2013 25 370-374 Rapid Isolation of Anti-angiogenic Constituents by Activity-Oriented Separation Method ZHUANG Wen-ting, ZHU Lu-ping, XIANG Cheng, HE Jing, LI Peng, LI Bao-cai Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 3c C23H18ClN5 ÏàËÆ¶È:66.6% Indian Journal of Chemistry Section B 2012 51B 1462-1469 Synthesis, reactions and anthelmintic activity of 1-[benzimidazol-2-yl]-4-formyl-3-[2¡ä (-substituted phenyl) indole-3-yl] pyrazoles Sharma, Kanti; Jain, Renuka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . [2-(4-Bromobenzyl)-1-thioxo-1,2,3,4-tetrahydro-¦Â-carbolin-9-yl]acetic acid C20H17O2N2SBr ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2012 20 356-367 Design, synthesis, and biological evaluation of novel (1-thioxo-1,2,3,4-tetrahydro-b-carbolin-9-yl)acetic acids as selective inhibitors for AKR1B1 Daisuke Minehira, Daisuke Takeda, Hirokazu Urata, Atsushi Kato, Isao Adachi, Xu Wang,Yuji Matsuya, Kenji Sugimoto, Mayuko Takemura, Satoshi Endo, Toshiyuki Matsunaga,Akira Hara, Jun Koseki, Kayo Narukawa, Shuichi Hirono, Naoki Toyooka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . N1-(2-bromophenyl)-N2-4-tolyloxalamide C15H13BrN2O2 ÏàËÆ¶È:61.1% Journal of Heterocyclic Chemistry 2006 43 1569-1574 A facile access to indigodianiles Christiane K¨¹hn,Rainer Beckert,Manfred Friedrich and Helmar Görls Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . 2-(N,N-dibenzylamino)-3-(benzotriazol-1-yl)-5-methoxy-2H-indazole C20H20N6O ÏàËÆ¶È:61.1% Journal of Heterocyclic Chemistry 2010 47 98-111 n-Butyllithium-mediated reactions of 1-(2-azidoarylmethyl)- 1H-benzotriazoles with alkyl halides Taehoon Kim and Kyongtae Kim Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 2-cyclohex-2-en-1-yl-1-methoxy-1H-indole C15H17NO ÏàËÆ¶È:61.1% Heterocycles 2006 68 2349-2356 Regioselective Reaction of 2-Indolylcyanocuprates with Electrophiles Minoru Ishikura,* Reina Uemura, Koji Yamada, and Reiko Yanada Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 1-Chloro-2(1-methylpropoxy)benzene ÏàËÆ¶È:61.1% Magnetic Resonance in Chemistry 2008 46 23-29 Origin of 13C complexation shifts in the adduct formation of 2-butyl phenyl ethers with a dirhodium tetracarboxylate complex (pages 23¨C29) Edison D¨ªaz G¨®mez and Helmut Duddeck Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . 2-methyl-6-(phenylsulfonyl)7-p-tolylpyrazolo[1,5-a]pyrimidine C20H17N3O2S ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2008 16 6344-6352 Synthesis and analgesic/anti-inflammatory evaluation of fused heterocyclic ring systems incorporating phenylsulfonyl moiety Mohamed R. Shaaban, Tamer S. Saleh, Abdelrahman S. Mayhoub, Ahmed Mansour, Ahmad M. Farag Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 2-(2,4-dimethylbenzyl-1H-indole-3-carbaldehy-de C18H17NO ÏàËÆ¶È:61.1% Indian Journal of Chemistry Section B 2011 50B 843-857 Studies on Lewis-acid mediated domino reaction of N-protected bromomethylindoles with arenes/heteroarenes Dhayalan, Vasudevan; Sureshbabu, Radhakrishnan; Mohanakrishnan, Arasambattu K Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . N-[1-(1-allyl-1H-indol-3-yl)-2,2,2-trichloroethyl]-trifluoromethanesulfonamide C14H12Cl3F3N2O2S ÏàËÆ¶È:61.1% Russian Journal of Organic Chemistry 2008 44 86-94 Reactions of N-(Polychloroethylidene)arene-and - trifluoromethanesulfonamides with indoles E. V. Kondrashov, E. V. Rudyakova, I. B. Rozentsveig, I. V. Ushakova and G. N. Rozentsveig, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 1,6-bis[3-(2,2,2-trichloro-1-trifluoromethylsul-fonylaminoethyl)-1H-indol-1-yl]hexane C28H26Cl6F6N4O4S2 ÏàËÆ¶È:61.1% Russian Journal of Organic Chemistry 2008 44 86-94 Reactions of N-(Polychloroethylidene)arene-and - trifluoromethanesulfonamides with indoles E. V. Kondrashov, E. V. Rudyakova, I. B. Rozentsveig, I. V. Ushakova and G. N. Rozentsveig, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . 2N-oxide-olivacine ÏàËÆ¶È:61.1% Natural Product Communications 2012 7 729-730 New Indole Alkaloid from Peschiera affinis (Apocynaceae) Allana Kellen L. Santos, Luciana L. Machado, Ayla Marcia C. Bizerra, Francisco Jos¨¦ Q. Monte, Gilvandete M. P. Santiago, Raimundo Braz-Filho and Telma L. G. Lemos Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 3f C24H21N5 ÏàËÆ¶È:61.1% Indian Journal of Chemistry Section B 2012 51B 1462-1469 Synthesis, reactions and anthelmintic activity of 1-[benzimidazol-2-yl]-4-formyl-3-[2¡ä (-substituted phenyl) indole-3-yl] pyrazoles Sharma, Kanti; Jain, Renuka Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (E)-2-(((3,5-bis(trifluoromethyl)phenyl)imino)methyl)-4-methylphenol C16H11F6NO ÏàËÆ¶È:61.1% Tetrahedron 2013 69 3810-3816 Formal [4+1] cycloaddition of camphor-derived sulfonium salts with aldimines: enantioselective synthesis of 2,3-dihydrobenzofurans Ying Cheng, Xiao-Qiang Hu, Shuang Gao, Liang-Qiu Lu, Jia-Rong Chen, Wen-Jing Xiao Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 9-hydroxyaristololactam I ÏàËÆ¶È:61.1% Acta Pharmaceutica Sinica 2011 46 188-192 A new aristolochic acid derivative from Asarum himalaicum XIE Bai-bo, SHANG Ming-ying *, WANG Xuan, CAI Shao-qing *, Kuo-hsiung LEE Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . butyl 2-((benzo[d]isoxazol-3-yl)methyl)-1H-benzimida-zole-1-carboxylate C20H19N3O3 ÏàËÆ¶È:57.8% Journal of Heterocyclic Chemistry 2007 44 685-691 Synthesis,anti-bacterial,anti-asthmatic and anti-diabetic activities of novel N-substituted-2-(benzo[d]isoxazol-3-ylmethyl)-1H-benzimidazoles Sanjay Dashrath Vaidya,Bobba Venkata Siva Kumar,Ramanatham Vinod Kumar,Umesh Nanasaheb Bhise and Uday Chandrakant Mashelkar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 21 . 2-((benzo[d]isoxazol-3-yl) methyl)-1-benzenesulfonyl-1H-benzimidazole C21H15N3O3S ÏàËÆ¶È:57.8% Journal of Heterocyclic Chemistry 2007 44 685-691 Synthesis,anti-bacterial,anti-asthmatic and anti-diabetic activities of novel N-substituted-2-(benzo[d]isoxazol-3-ylmethyl)-1H-benzimidazoles Sanjay Dashrath Vaidya,Bobba Venkata Siva Kumar,Ramanatham Vinod Kumar,Umesh Nanasaheb Bhise and Uday Chandrakant Mashelkar Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 22 . 2-(3-nitrophenyl)-3-p-tolyl-3,4-dihydro-2H-benzo[e][1,3]oxazine C21H18N2O3 ÏàËÆ¶È:57.8% Journal of Heterocyclic Chemistry 2011 48 255-260 Synthesis of 2,3-diaryl-3,4-dihydro-2H-1,3-benzoxazines and their fungicidal activities Zilong Tang, Weiwen Chen, Zhonghua Zhu and Hanwen Liu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 23 . 6-(4-fluorophenyl)-7-methyl-5,6-dihydroindolo[1,2-a]quinoxaline C22H17FN2 ÏàËÆ¶È:57.8% European Journal of Organic Chemistry 2011 6998-7010 Lewis Acid-Catalyzed Selective Synthesis of Diversely Substituted Indolo- and Pyrrolo[1,2-a]quinoxalines and Quinoxalinones by Modified Pictet¨CSpengler Reaction Akhilesh K. Verma, Rajeev R. Jha, V. Kasi Sankar, Trapti Aggarwal, Rajendra P. Singh and Ramesh Chandra Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 24 . compound 3b C23H17ClFN5 ÏàËÆ¶È:57.8% Indian Journal of Chemistry Section B 2012 51B 1462-1469 Synthesis, reactions and anthelmintic activity of 1-[benzimidazol-2-yl]-4-formyl-3-[2¡ä (-substituted phenyl) indole-3-yl] pyrazoles Sharma, Kanti; Jain, Renuka Structure 13C NMR ̼Æ×Ä£Äâͼ |
4Â¥2013-11-13 08:09:57













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