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²éѯ½á¹û£º¹²²éµ½12¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . arborescidine B C16H17BrN2 ÏàËÆ¶È:50% Journal of Natural Products 1993 Vol 56 99 Brominated Indole Alkaloids from the Marine Tunicate Pseudodistoma arborescens Mohammed Chbani, Mary Païs, Jean-Marc Delauneux, C¨¦cile Debitus Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . baishouwubenzophenone C16H14O6 ÏàËÆ¶È:50% Acta Pharmaceutica Sinica 1988 Vol 23 276-280 STUDIES ON CONSTITUENTS OF CHINESE TRADITIONAL DRUG BAISHOUWU (CYNANCHUM AURICULATUM ROYLE EX WIGHT) SS Gong; CD Liu; SL Liu; YR Du; W Kang and XQ Dong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 4¦Â-hydroxyeudesma-2,11(13)-dien-5¦ÁH-12-oic acid ÏàËÆ¶È:50% Phytochemistry 1991 30 3653-3655 Oxygenated nerolidol esters and eudesmane acids fromInula viscosa Juan F. Sanz, Carmen Ferrando, J. Alberto Marco Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . Compound 12 ÏàËÆ¶È:50% Journal of the American Chemical Society 1976 98 3645-3655 Gneeral Methods of Synthesis of Indole Alkaloids.14.1,2 Short Routes of Construction of Yohimboid and Ajmalicinoid Alkaloid Systems and Theis 13C Nuclear Magnetic Resonance Spectral Analysis Ernest Wenkert,Ching-Jer Chang,H.P.S Chawla W.Cochran, Edward W.Hagaman,James C.King, and Kazuhiko Orito Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . apocynol A C13H20O3 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2001 49 845-848 Medicinal Foodstuffs. XXIV. Chemical Constituents of the Processed Leaves of Apocynum venetum L.: Absolute Stereostructures of Apocynosides I and II Toshiyuki MURAKAMI, Akinobu KISHI, Hisashi MATSUDA, Masao HATTORI and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 3-(2,3-dimethoxy-4-methylphenyl)-3-methylpent-4-enal C15H20O3 ÏàËÆ¶È:50% Tetrahedron 2006 62 9393-9402 Structure revision of HM-3, an aromatic sesquiterpene isolated from the phytopathogenic fungus Helicobasidium mompa. First total syntheses of HM-3 and HM-4 A. Srikrishna, P.C. Ravikumar Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (¡À)-arborescidine B C16H17N2Br ÏàËÆ¶È:50% Tetrahedron 1998 54 6135-6146 Synthesis of the brominated marine alkaloids (¡À)-arborescidine A, B and C Brigitte E.A. Burm, Michaël M. Meijler, Jacco Korver, Martin J. Wanner, Gerrit-Jan Koomen Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 6,7-dimethoxy-1-methyl-2(1H)-quinoxalinone-3-propionylcarboxylic acid methyl ester ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 1998 36 300-302 Complete 13C and 1H spectral assignments of certain substituted quinoxalinones Val¨¦rie Rampont-Placidi, Benoit Cossec, Marie-Th¨¦r¨¨se Brondeau and Pierre Mutzenhardt Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Methyl 2-Hexylbenzofuran-3-carboxylate C16H20O3 ÏàËÆ¶È:50% Synthesis 2012 44 1825−1832 Cyclization¨CCarbonylation¨CCyclization Coupling Reactions of N-Propargylanilines and o-Alkynylphenols with Palladium(II)¨CBisoxazoline Catalysts Kusakabe, Taichi; Sekiyama, Emika; Ishino, Yukari; Motodate, Satoshi; Kato, Shigeki; Mochida, Tomoyuki; Kato, Keisuke Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Jasminoside B ÏàËÆ¶È:50% Lishizhen Medicine and Materia Medica Research 2013 24 1599-1603 »ÆÁ¬½â¶¾ÌÀ»¯Ñ§³É·Ö¼°ÆäÉñ¾Ï¸°û±£»¤×÷ÓÃÑо¿ ÑîÑô, ÕÔº£Óþ, Ëν¨·¼, Íõºê½à, Ñ, ˾ÄÏ, ÁõÇìɽ, ±ß±¦ÁÖ* Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 12 ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 1992 30 678-681 13C NMR spectra of eudesmane derivatives J. Alberto Marco, Juan F. Sanz and Miguel Carda Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-(N,N-Diethylamino)ethyl 6-acetyl-5-hydroxy-2-methyl-3-benzofurancarboxylate C18H23NO5 ÏàËÆ¶È:50% Monatshefte f¨¹r Chemie 2013 144 1679-1689 Microwave-assisted preparation and antimicrobial activity of O-alkylamino benzofurancarboxylates Kinga Ostrowska, Elżbieta Hejchman, Irena Wolska, Hanna Kruszewska, Dorota Maciejewska Structure 13C NMR ̼Æ×Ä£Äâͼ |
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