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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£º¹²²éµ½65¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 5-(methoxymethyl)-1H-pyrrole-2-carbaldehyde C7H9NO2 ÏàËÆ¶È:62.5% Journal of Natural Products 2005 68 1066-1070 Nitrogen-Containing Compounds from Salvia miltiorrhiza Ming-Jaw Don, Chien-Chang Shen, Yun-Lian Lin, Wan-Jr Syu, Yi-Huei Ding, and Chang-Ming Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (E)-4-(tert-Butyldimethylsilyl)oxy-3-methyl-but-2-en-1-ol ÏàËÆ¶È:62.5% Bioorganic & Medicinal Chemistry Letters 2003 13 1257-1260 Replacing the pyrophosphate group of HMB-PP by a diphosphonate function abrogates Its potential to activate human ¦Ã¦Ä T cells but does not lead to competitive antagonism Armin Reichenberg, Martin Hintz, Yvonne Kletschek, Tanja Kuhl, Christian Haug, Rosel Engel, Jens Moll, Dmitry N. Ostrovsky, Hassan Jomaa, Matthias Eberl Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . compound 5h ÏàËÆ¶È:62.5% Tetrahedron Letters 2005 46 7247-7248 Efficient cyclopropanation of active methylene compounds. A serendipitous discovery Veera Reddy Arava, Udaya Bhaskara Rao Siripalli, Pramod Kumar Dubey Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 5-methoxymethyl-1H-pyrrole-2-carbaaldehyde C7H9NO2 ÏàËÆ¶È:62.5% Natural product sciences 2011 17 181-182 A New Pyrrole Constituent from the Fruits of Lycium chinense Jeon, Wan-Soo; Kim, E. Ray; Chin, Young-Won; Kim, Jin-Woong Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 5-¼×Ñõ¼×»ù-1H-ßÁ¿©-2-¼×È© ÏàËÆ¶È:62.5% Journal of Tropical and Subtropical Botany 2010 18 564-568 Chemical Constituents from Isodon lophanthoides var. gracilif lora LIANG, Yao, guang, XU, Xinya, XIE, Hai, hui, LIN, Qing, WEI, Xiao, yi Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 5-((tert-Butyldimethylsilyloxy)methyl)-1H-pyrrole-2-carbaldehyde C12H21NO2Si ÏàËÆ¶È:55.5% Organic Letters 2011 Vol. 13, No. 20 5452-5455 Total Synthesis and Stereochemical Revision of Acortatarins A and B Gangarajula Sudhakar, Vilas D. Kadam, Shruthi Bayya, Gavinolla Pranitha, and Bharatam Jagadeesh Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . transtorine C10H7O3N ÏàËÆ¶È:50% Journal of Natural Products 1998 61 262-263 Transtorine, a New Quinoline Alkaloid from Ephedra transitoria Suleiman Al-Khalil Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-Methylsulfanyl-3-phenyl-3,5-dihydroimidazol-4-one C10H10N2OS ÏàËÆ¶È:50% Molecules 2004 9 867-875 Reactivity of 2-Thiohydantoins Towards Various Electrophilic Reagents: Applications to the Synthesis of New 2-Ylidene-3, 5-dihydro-4H-imidazol-4-ones. Jean-Ren¨¦ Ch¨¦rouvrier, François Carreaux and Jean P. Bazureau Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 5-hydroxymethyl-2-furancarboxaldehyde ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2009 34 2200-2202 Chemical constituents of Lobelia chinensis HAN Jinglan, Zhang Fengling, LI Zhihong, DU Guanhua, QIN Hailin Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 5-(hydroxymethyl)furfural ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2008 33 1272-1274 Studies on chemical constituents of Dioscorea opposita BAI Bing, LI Mingjing, WANG Yong, LIU Xiuhua Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . herierin III C8H10O4 ÏàËÆ¶È:50% Acta Pharmaceutica Sinica 1990 Vol 25 522-525 ISOLATION AND IDENTIFICATION OF TWO NEW PYRONE COMPOUNDS FROM THE CULTURE OF HERICTUM ERINACEUS FG Qian; GY Xu; SJ Du and MH Li Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 1-(3-Hydroxyphenyl)-4(methoxyphenyl)-2,6-diphenyl-1,4-dihydropyridine C30H25NO2 ÏàËÆ¶È:50% Canadian Journal of Chemistry 2006 84 1064-1073 A new and efficient one-pot solid-supported synthesis of 1,2,4,6-tetraaryl-1,4-dihydropyridines Anil K. Verma, Summon Koul, Tej K. Razdan, and Kamal K. Kapoor Structure 13C NMR ̼Æ×Ä£Äâͼ |

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