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jiayanlai: ½ð±Ò+10, ¡ïÓаïÖú 2014-10-06 20:25:38
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jiayanlai: ½ð±Ò+10, ¡ïÓаïÖú 2014-10-06 20:25:38
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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£º¹²²éµ½42¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . N-[4-(dimethylamino)-2-butynyl]-4-methyl-2-azetidinone oxalate C10H16N2O ÏàËÆ¶È:60% Journal of Medicinal Chemistry 1990 33 580-584 beta.-Lactam analogs of oxotremorine. 3- and 4-Methyl-substituted 2-azetidinones Bjoern M. Nilsson, Bjorn Ringdahl, Uli Hacksell Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . (Z)-ethyl (5-acetoxy-3-methyl-4-oxothiazolidine-2-ylidene)ethanoate C10H13NO5S ÏàËÆ¶È:60% Tetrahedron 2013 69 9819-9825 Unusual mode of reactivity of 2-alkylidene-4-oxothiazolidine S-oxides under the Pummerer reaction conditions Original Research Article Zdravko Džambaski, Đorđe Toljić, Bojan Bondžić, Rade Marković, Marija Baranac-Stojanović Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-methyl-4a-benzyl-4a,5-dihydrolumiflavin ÏàËÆ¶È:53.8% Helvetica Chimica Acta 1980 63 2187-2201 A Comparative 13C-NMR. Study on Various Reduced Flavins Cees G. Van Schagen, Franz M¨¹ller Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . antiprotealide C12H18ClNO4 ÏàËÆ¶È:50% Journal of Natural Products 2009 72 295-297 Antiprotealide Is a Natural Product Rama Rao Manam, Venkat R. Macherla, Ginger Tsueng, Chris W. Dring, Jeffrey Weiss, Saskia T. C. Neuteboom, Kin S. Lam, and Barbara C. Potts Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-O-acetyl-7-O-methylpyranonigrin A C13H13NO6 ÏàËÆ¶È:50% Journal of Natural Products 2007 70 1180-1187 Reassessing the Structure of Pyranonigrin Gerhard Schlingmann,Tohru Taniguchi, Haiyin He, Ramunas Bigelis, Hui Y. Yang, Frank E. Koehn, Guy T. Carter, and Nina Berova Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . cyclo-(Leu-Thr) C10H18O3N2 ÏàËÆ¶È:50% Acta Botanica Yunnanica 2003 25(3) 366-368 Cyclodipeptides of Panax notoginseng and Lactams of Panax ginseng TAN Ning-Hua,WANG huang-Ming, YANG Ya-Bin,HE Ming Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . virginae butanolide F C9H16O4 ÏàËÆ¶È:50% Chinese Chemical Letters 2006 17 1466-1468 A New Virginae Butanolide from Streptomyces sp. Xiang LI, Yi Nan ZHENG, Wen Han LIN, Isabel SATTLER Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 7,10,10-Trimethyl-3-selena-4,5-diaza-tricyclo[5.2.1.02,6]deca-2(6),4-diene C10H14N2Se ÏàËÆ¶È:50% Molecules 2004 9 957-967 New 1, 2, 3-Selenadiazole and 1, 2, 3-Thiadiazole Derivatives Mousa Al-Smadi and Samer Ratrout Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 7,10,10-Trimethyl-3-thia-4,5-diaza-tricyclo[5.2.1.02,6]deca-2(6),4-diene C10H14N2S ÏàËÆ¶È:50% Molecules 2004 9 957-967 New 1, 2, 3-Selenadiazole and 1, 2, 3-Thiadiazole Derivatives Mousa Al-Smadi and Samer Ratrout Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 1-(2-Cyanoethyl)-3-(2-ethoxy-2-oxoethyl)-1H-imidazol-3-ium bromide ÏàËÆ¶È:50% Molecules 2009 14 403-411 Microwave Assisted Reactions of Some Azaheterocylic Compounds Gheorghita Zbancioc, Vasilichia Bejan, Marian Risca, Costel Moldoveanu and Ionel I. Mangalagiu Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (S)-5-isopropyl-5,6-dihydro-2H-1,4-oxazin-2-one ÏàËÆ¶È:50% Heterocycles 2008 76 747-757 A Simple Chiral Template for the Synthesis of Fuctionalized ¦Á-Arylglycine Derivatives Hiyoku Nakata, Takahiro Imai, Satoshi Yokoshima, and Tohru Fukuyama Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Compound 6 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry Letters 2010 20 2665-2667 Shoukath M. Ali, Ateeq Ahmad, Syed Shahabuddin, Moghis U. Ahmad, Saifuddin Sheikh, Imran Ahmad Shoukath M. Ali, Ateeq Ahmad, Syed Shahabuddin, Moghis U. Ahmad, Saifuddin Sheikh, Imran Ahmad Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . Cyclo (L-Val-L-Ala) ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2009 47 366-370 1H and 13C NMR assignments of eight nitrogen containing compounds from Nocardia alba sp.nov (YIM 30243T) (pages 366¨C370) Zhang-Gui Ding, Jiang-Yuan Zhao, Pei-Wen Yang, Ming-Gang Li, Rong Huang, Xiao-Long Cui and Meng-Liang Wen Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound Z-7 C11H19NO4 ÏàËÆ¶È:50% Tetrahedron Letters 2003 44 4361-4364 Excess sodium ions improve Z selectivity in Horner¨CWadsworth¨CEmmons olefinations with the Ando phosphonate Petri M. Pihko, Taina M. Salo Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound 4c C11H21N3O ÏàËÆ¶È:50% Tetrahedron Letters 2003 44 8479-8481 Asymmetric Strecker synthesis by addition of trimethylsilyl cyanide to aldehyde SAMP-hydrazones Dieter Enders, Michael Moser Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . »·(çÓ-ÀÒ)¶þëÄ C14H18N2O3 ÏàËÆ¶È:50% Journal of China Pharmaceutical University 2005 36 523-525 Aqueous Constituents from Stellaria Media(L.) Cyr. HU Yong-Mei; WANG Hao; YE Wen-Cai; LIU Ge Structure 13C NMR ̼Æ×Ä£Äâͼ |

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