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jiangchunyong: ½ð±Ò+1, лл 2013-10-28 15:48:51
zhanchuan: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-10-28 20:34:01
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jiangchunyong: ½ð±Ò+1, лл 2013-10-28 15:48:51
zhanchuan: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-10-28 20:34:01
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²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½32¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5a¦Á,6,9,9a¦Â,10-Pentahydro-10¦Â-hydroxy-7-methylanthra[1,2-d]-[1,3]dioxol-5-one C16H16O4 ÏàËÆ¶È:75% Journal of Natural Products 2012 75 2076-2081 PPAR¦Ã Agonist from Chromolaena odorata Man-Li Zhang, Dianne Irwin, Xiao-Ning Li, Françoise Sauriol, Xiao-Wei Shi, Yu-Fang Wang, Chang-Hong Huo, Li-Geng Li, Yu-Cheng Gu, and Qing-Wen Shi Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2,10¦Â-dibromochamigra-2,7-dien-9a-ol ÏàËÆ¶È:53.3% Helvetica Chimica Acta 2009 92 1873-1879 Halogenated Sesquiterpenes from the Marine Red Alga Laurencia saitoi (Rhodomelaceae) Nai-Yun Ji, Xiao-Ming Li, Ke Li, Bin-Gui Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . diethyl 3-(1H-1,2,3-benzotriazol-1-yl)-1-[(ethoxycarbothioyl)thio]propyl phosphonate C16H24N3O4PS2 ÏàËÆ¶È:53.3% Heterocycles 2001 54 301-308 Xanthate Mediated Generation of the Benzotriazol-1-yl-methyl Radical and Its Subsequent Addition to a Variety of Olefins Alan R. Katritzky,* Martin A. C. Button, and Sergey N. Denisenko Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (+)-helminthogermacrene C15H24 ÏàËÆ¶È:50% Phytochemistry 2004 65 199-206 Sesquiterpenes of the liverwort Scapania undulata Adewale Martins Adio, Claudia Paul, Petra Kloth, Wilfried A. König Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . Haplacutine F C18H23NO ÏàËÆ¶È:50% Phytochemistry 2009 70 1055-1061 Accelerated dereplication of crude extracts using HPLC¨CPDA¨CMS¨CSPE¨CNMR: Quinolinone alkaloids of Haplophyllum acutifolium Dan Staerk, Julie R. Kesting, Majid Sairafianpour, Matthias Witt, Javad Asili, Seyed A. Emami, Jerzy W. Jaroszewski Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . trans-3-Benzo[1,3]dioxol-5-yl-N-isopropyl-acrylamide C13H15NO3 ÏàËÆ¶È:50% Molecules 2009 14 3833-3843 Amides from Piper capense with CNS Activity ¨C A Preliminary SAR Analysis Mikael E. Pedersen, Bjørn Metzler, Gary I. Stafford, Johannes van Staden, Anna K. Jäger and Hasse B. Rasmussen Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2-(4-methoxybenzyliden)-4,4-dimethyl-3-oxopentanonitrile C15H17NO2 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2006 43 299-306 Microwave-assisted three-component synthesis and in vitro antifungal evaluation of 6-cyano-5,8-dihydropyrido[2,3-d]pyrimidin-4(3H)-ones Jairo Quiroga,Carlos Cisneros,Braulio Insuasty,Rodrigo Abon¨ªa,Silvia Cruz,Manuel Nogueras,Jos¨¦ Manuel de la Torre,Maximiliano Sortino and Susana Zacchino Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (10a'S)-2',3',5',6',7',10'-Hexahydro-10a'H-spiro[1,3-dithiolane-2,1'-pyrrolo[1,2-a]azocin]-10a'-ylmethanol C13H21NOS2 ÏàËÆ¶È:50% Heterocycles 2006 68 47-58 Concise Highly Enantioselective Cascade Synthesis of Azacyclooctene Alkaloids with a Quaternary Stereocenter Daniele Muroni, Antonio Saba,* and Nicola Culeddu Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Limonene ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2001 39 621-624 Enantiomeric differentiation of terpenic olefins by carbon-13 NMR using chiral binuclear shift reagents Nicolas Baldovini, F¨¦lix Tomi and Joseph Casanova Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . (¡À)-N-allyl-5-benzoyl-2-pyrrolidinone C14H15NO2 ÏàËÆ¶È:50% Tetrahedron 2012 68 3692-3700 Application of the intramolecular PIFA-mediated amidation of alkynes to the synthesis of substituted indolizidinones Leticia M. Pardo, Imanol Tellitu, Esther Dom¨ªnguez Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 5a C11H12N2S ÏàËÆ¶È:50% Heterocycles 2000 53 613-620 Synthesis and Structural Features of New Cyclofunctionalized Benzimidazoles Alba Chimirri,* Anna Maria Monforte, Pietro Monforte, Francesco Nicol¨°, Angela Rao, and Maria Zappal¨¤ Structure 13C NMR ̼Æ×Ä£Äâͼ |

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