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13C NMR ( cd3od) 4.56,10.78, 22.24,57.17,120.38, 122.85, 124.10,159.81 |
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yyzhou: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-06-15 15:21:18
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yyzhou: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-06-15 15:21:18
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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£º¹²²éµ½9¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-Chloro-N-phenylpropanamide ÏàËÆ¶È:50% Chemistry of Natural Compounds 2011 Vol. 47, No. 4 541-544 BIOACTIVE METABOLITES FROM Penicillium sp. P-1,A FUNGAL ENDOPHYTE IN Huperzia serrata You-Min Ying, Zha-Jun Zhan, Zhi-Shan Ding,and Wei-Guang Shan Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 5a ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 5833-5835 Synthesis and reactivity of benzoxa(thia)zol-2-thiones: new route to 2-alkylthiobenzoxa(thia)zoles Abdallah Harizi, Anis Romdhane, Zine Mighri Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . dipropyl ethenylmalonate C11H18O4 ÏàËÆ¶È:50% Organic letters 2001 3 789-790 GaCl3-Promoted Ethenylation of Silylated ¦Â-Dicarbonyl Compound with Silylethyne. Synthesis of Ethenylmalonate Mieko Arisawa, Kensuke Akamatsu, and Masahiko Yamaguchi Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (R)-(-)-1-(benzofuran-2-yl)ethanol C10H10O2 ÏàËÆ¶È:50% Heterocycles 2001 55 569-577 Enantioselective Synthesis of 2- and 3-Benzofuryl ¦Â-Amino Alcohols Marek Zaidlewicz,* Aldona Chechlowska, Andrzej Prewysz-Kwinto, and Andrzej Wojtczak Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . compound 9 C8H8N2O2 ÏàËÆ¶È:50% Heterocycles 2000 52 719-732 Synthesis of Optically Pure 1-(2-Pyridinyl)ethylamine and 4-(2-Pyridinyl)-1,3-oxazolin-2-one Jun'ichi Uenishi,* Takao Hiraoka, Kyoko Yuyama, and Osamu Yonemitsu Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 4,5,6,7-tetrahydro-2-phenyl-isoindole C14H15N ÏàËÆ¶È:50% Tetrahedron 1989 45 3189-3202 Functionalized chloroenamines in aminocyclopropane synthesis I. ¡ª bicyclic and pentacyclic lactams from carbamoylated chloroenamines Peter Altmeier, Elmar Vilsmaier, Gotthelf Wolmershäuser Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . N-(1-silatranylmethyl)carbazole C19H22N2O3Si ÏàËÆ¶È:50% Russian Journal of Organic Chemistry 2003 39 1458-1466 N-Silatranylmethyl Derivatives of Pyrrole, Indole, and Carbazole M. G. Voronkov, O. M. Trofimova, V. K. Turchaninov, E. A. Zel'bst and Yu. I. Bolgova, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 5-bromo-3-iodo-1H-indole C8H5BrIN ÏàËÆ¶È:50% Tetrahedron 2012 68 6269-6275 A convenient iodination of indoles and derivatives Salha Hamri, Jose Rodr¨ªguez, Joan Basset, G¨¦rald Guillaumet, M. Dolors Pujol Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . (¡À)-2-(allylsulfinyl)pyridine C8H9NOS ÏàËÆ¶È:50% European Journal of Organic Chemistry 2010 6409-6416 Enzymatic Synthesis of Novel Chiral Sulfoxides Employing Baeyer¨CVilliger Monooxygenases Ana Rioz-Mart¨ªnez, Gonzalo de Gonzalo, Daniel E. Torres Pazmiño, Marco W. Fraaije and Vicente Gotor Structure 13C NMR ̼Æ×Ä£Äâͼ |

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