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C13NMR(CDCL3): 15.4,15.8,21.3,28.8,32.7,37.4,52.2,126.6,126.8,136.2,140.5,145.8,146.4,148.6,149.3,149.8,152.4,167.0,167.3 ÒÑÃ÷È·ËùÇ󻯺ÏÎïÊÇÎÞɫ͸Ã÷ÒºÌå×´ÉúÎï¼î£¬ÉÏ´«¸½¼þΪËùÇ󻯺ÏÎïµÄ̼Æ×ºÍÇâÆ×µÄÆ×ͼ |
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²éѯ½á¹û£º¹²²éµ½40¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 12-ethyl-5,6,13,14-tetrahydro-2-hdyroxy-3-methoxy-8H-isoquino[2.1-b][2.7]naphthyridin-8-one C19H20N2O3 ÏàËÆ¶È:68.4% Canadian Journal of Chemistry 1987 65 2362-2368 8H-Isoquino[2,1-b][2,7]naphthyridin-8-ones: synthesis of the Alangium alkaloids, alangimaridine and alangimarine Jahangir, Michael A. Brook, David B. MacLean, Herbert L. Holland Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 12a ÏàËÆ¶È:66.6% Journal of Natural Products 2014 77 1021-1030 Spiromastixones A¨CO, Antibacterial Chlorodepsidones from a Deep-Sea-Derived Spiromastix sp. Fungus Siwen Niu, Dong Liu, Xinxin Hu, Peter Proksch, Zhongzhe Shao, and Wenhan Lin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . austrodimerine C21H27N3O5 ÏàËÆ¶È:65% Phytochemistry 1998 47 825-832 Monoterpene alkaloids, iridoids and phenylpropanoid glycosides from Osmanthus austrocaledonica Rabah Benkrief, Yvonne Ranarivelo, Alexios-Leandros Skaltsounis, Francois Tillequin, Michel Koch, Jacques Pusset, Thierry S¨¦venet Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . compound 4l C24H34N4O6 ÏàËÆ¶È:65% European Journal of Organic Chemistry 2011 4293-4297 Synthesis of Various Chiral 1,2,4-Triazole-Containing -Amino Acids from Aspartic or Glutamic Acids Anne-Laure Blayo, Fr¨¦d¨¦ric Brunel, Jean Martinez and Jean-Alain Fehrentz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ketoheterophyllin A C20H24O7 ÏàËÆ¶È:65% Chemical & Pharmaceutical Bulletin 2014 62 1092-1099 Germacranolides and Their Diversity of Eupatorium heterophyllum Collected in P. R. China Yoshinori Saito, Tomomi Mukai, Yuko Iwamoto, Makiko Baba, Koji Takiguchi, Yasuko Okamoto, Xun Gong, Takayuki Kawahara, Chiaki Kuroda, Motoo Tori Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . ethyl 2,7,7-trimethyl-5-oxo-4-phenyl-1,4,5,6,7,8-hexahydroquinoline-3-carboxylate C21H25NO3 ÏàËÆ¶È:63.1% Indian Journal of Chemistry Section B 2008 47B 1084-1090 Hantzsch synthesis of polyhydroquinolines - A simple,efficient and neat protocol Arumugam,Pandurangan; Perumal,Paramasivan T Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . N,N-Dihexyl-(5-{(E)-2-[5-((E)-2-thiazol-2-yl-vinyl)thiazol-2-yl]vinyl}thiazol-2-yl)amine C25H34N4S3 ÏàËÆ¶È:63.1% Zeitschrift f¨¹r Naturforschung B 2007 62 1525-1529 Conjugated Compounds Based on Vinylthiazole Units H. Meier, F. Nicklas, and R. Petermann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . dimethyl 6-[(diphenoxyphosphoryl)oxy]-3-hydroxy-4-pentylphthalate C27H29O9P ÏàËÆ¶È:63.1% European Journal of Organic Chemistry 2011 7140-7147 Olefin-Metathesis-Based Synthesis of Furans by an RCM/Deprotonation/Phosphorylation Sequence and Their Diels¨CAlder Reactions Bernd Schmidt and Diana Geißler Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 39,42-diacetoxy-5,17,23,35-tetra-tert-butyl-37,38,40,41-tetra-ethoxy-11,29-dinitrocalix[6]arene C70H86N2O12 ÏàËÆ¶È:63.1% European Journal of Organic Chemistry 2010 7005-7011 Microwave-Assisted Synthesis of a Nitro-m-xylylenedioxycalix[6]arene Building Block Functionalized at the Upper Rim Hitos Gal¨¢n, Javier de Mendoza and Pilar Prados Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . schizanthine I C19H27NO6 ÏàËÆ¶È:63.1% Heterocycles 1988 27 1887-1897 Tropane Alkaloids from Schizanthus pinnatus Gabriel de la Fuente, Mat¨ªas Reina, Orlando Muñoz, Aurelio San Mart¨ªn, and Jean-Pierre Girault Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 12-ethyl-5,6,13,14-tetrahydro-2,3-dimethoxy-8H-isoquino[2.1-b][2.7]naphthyridin-8-one C20H22N2O3 ÏàËÆ¶È:63.1% Canadian Journal of Chemistry 1987 65 2362-2368 8H-Isoquino[2,1-b][2,7]naphthyridin-8-ones: synthesis of the Alangium alkaloids, alangimaridine and alangimarine Jahangir, Michael A. Brook, David B. MacLean, Herbert L. Holland Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . formosusin A C17H25NO3 ÏàËÆ¶È:63.1% Bioorganic & Medicinal Chemistry 2014 22 1070-1076 Formosusin A, a novel specific inhibitor of mammalian DNA polymerase ¦Â from the fungus Paecilomyces formosus Yoshiyuki Mizushina, Hiroe Suzuki-Fukudome, Toshifumi Takeuchi, Kenji Takemoto, Isoko Kuriyama, Hiromi Yoshida, Shinji Kamisuki, Fumio Sugawara Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . [1-(4-nitrophenyl)-1H-1,2,3-triazol-4-yl]methyl 3,4-dihydro-4-(4-hydroxyphenyl)-2-oxo-6-propyl-1H-pyrimidine-5-carboxylate C23H22N6O6 ÏàËÆ¶È:63.1% Helvetica Chimica Acta 2014 97 375-383 One-Pot Synthesis of (1,2,3-Triazolyl)methyl 3,4-Dihydro-2-oxo-1H-pyrimidine-5-carboxylates as Potentially Active Antimicrobial Agents (pages 375¨C383) Minoo Dabiri, Peyman Salehi, Mahboubeh Bahramnejad, Majid Koohshari and Atousa Aliahmadi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 2-Amino-5-benzoyl-N-butyl-4-(pyridin-2-yl)-1Hpyrrole-3-carboxamide C21H22N4O2 ÏàËÆ¶È:63.1% Chemical Biology & Drug Design 2010 75 277-283 Design of a Versatile Multicomponent Reaction Leading to 2-amino-5-ketoaryl pyrroles Kan Wang and Alexander Dömling Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . dehydrocannabifuran ÏàËÆ¶È:61.9% Planta Medica 2008 74 267-272 Isolation and Characterization of New Cannabis Constituents from a High Potency Variety Mohamed M. Radwan, Samir A. Ross, Desmond Slade, Safwat A. Ahmed, Fazila Zulfiqar,Mahmoud A. ElSohly Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . Ethyl 3-Acetoxy-9-methyl-7-(4-nitrophenyl)-6-oxo-7,8-dihydro-6H-dibenzo[b,d]pyran-8-carboxylate C25H21NO8 ÏàËÆ¶È:60.8% Synthesis 2012 44 2385−2395 Synthesis of 6H-Dibenzo[b,d]pyran-6-one Derivatives via Coumarin-Fused Cyclohexa-1,3-diene Intermediates Chen, Chao-Yue; Zhao, Yong-Sheng; Xiang, Chang-Bing; Huang, Zhi-Zhen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . argutane B C20H22N2O2 ÏàËÆ¶È:60% Helvetica Chimica Acta 2007 Vol. 90 2151 Two Novel Monoterpene Alkaloid Dimers from Incarvillea arguta Jian-Jun Fu, Hui-Zi Jin, Yun-Heng Shen, Wei-Dong Zhang, Wen-Zheng Xu, Qi Zeng, and Shi-Kai Yan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . lecocarpinolide ÏàËÆ¶È:60% Helvetica Chimica Acta 2005 Vol. 88 160 Novel Sesquiterpenoids from Siegesbeckia orientalis Ying Xiang, Cheng-Qi Fan, Jian-Min Yue Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . drypetenone C C20H22O5 ÏàËÆ¶È:60% Journal of Natural Products 2001 64 707-709 Chemical Constituents from Drypetes littoralis |

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