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ÒÔºóÇë×¢Òâ¸ñʽ£ºÊýÖµ´ÓСµ½´ó£¬ÒÔÓ¢ÎĶººÅ¸ô¿ª£¬ÊýÖµ¼äÎÞ¿Õ¸ñ¡£¡£¡£ ²éѯ½á¹û£º¹²²éµ½4541¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . salprionin C20H24O3 ÏàËÆ¶È:79.1% Phytochemistry 1995 40 1469-1471 De-O-ethylsalvonitin and salprionin, two further diterpenoids from Salvia prionitis Long-Ze Lin, Geoffrey A. Cordell, Pin Lin Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . inulacappolide C22H30O7 ÏàËÆ¶È:66.6% Chemical & Pharmaceutical Bulletin 2007 55(8) 1258-1260 Cytotoxic Germacranolide Sesquiterpene from Inula cappa Hong-Gang XIE,Hong CHEN,Bo CAO,Hong-Wu ZHANG,and Zhong-Mei ZOU Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . pirolatin ÏàËÆ¶È:66.6% Phytochemistry 1985 24 1857-1859 Structure of renifolin and reconfirmation of the structure of pirolatin Hiroyuki Inouye, Kenichiro Inoue Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,4-O-Isopropylidene-¦Â-D-galactopyranosyl)-(1¡ú4)-3-oallyl-6-O-benzyl-2-deoxy-2-phthalimido-¦Â-D-glucopyranosyl azide ÏàËÆ¶È:66.6% Bioorganic & Medicinal Chemistry 1997 5 1-19 Glycosyl azides as building blocks in convergent syntheses of oligomeric lactosamine and Lewisx saccharides Wolfgang Bröder, Horst Kunz Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . methyl (R,S,R)-2-(2,6,10-trimethyl-1(E),5(E),9-tridecatrienyl)-5-[(phenylmethoxy)methyl]-2,3,4,5-tetrahydro-3-furancarboxylate C28H40O4 ÏàËÆ¶È:66.6% The Journal of Organic Chemistry 1997 62 6603-6607 Specific C−C Bond Construction by Remote C−H Activation: Synthesis of (− -trans-CembranolideDouglass F. Taber and Ying Song Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . compound 26a ÏàËÆ¶È:66.6% Journal of the American Chemical Society 2002 124 10416-10426 Synthesis, Structure, and Biological Evaluation of Novel N- and O-Linked Diinositols Bernhard J. Paul, Jerremey Willis, Theodore A. Martinot, Ion Ghiviriga, Khalil A. Abboud, and Tomas Hudlicky Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 26b ÏàËÆ¶È:66.6% Journal of the American Chemical Society 2002 124 10416-10426 Synthesis, Structure, and Biological Evaluation of Novel N- and O-Linked Diinositols Bernhard J. Paul, Jerremey Willis, Theodore A. Martinot, Ion Ghiviriga, Khalil A. Abboud, and Tomas Hudlicky Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . epothilone C5 C26H37NO5S ÏàËÆ¶È:65.3% Journal of Natural Products 2001 64 847-856 New Natural Epothilones from Sorangium cellulosum, Strains So ce90/B2 and So ce90/D13: Isolation, Structure Elucidation, and SAR Studies Ingo H. Hardt,Heinrich Steinmetz, Klaus Gerth, F. Sasse, Hans Reichenbach, and Gerhard Höfle Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 11 C38H50O4Si ÏàËÆ¶È:65.3% Natural Product Communications 2013 8 929-934 A New Variant of Fused Cyclic Ether Synthesis Based on Ireland-Claisen Rearrangement and RCM Daisuke Domon, Kenshu Fujiwara, Natsumi Kawamura, Ryo Katoono, Hidetoshi Kawai and Takanori Suzuki Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 7¦Â-O-benzylrosmanol C27H32O5 ÏàËÆ¶È:64% Journal of Natural Products 2009 72 1385-1389 Semisynthesis and Biological Evaluation of Abietane-Type Diterpenes. Revision of the Structure of Rosmaquinone Joaquin G. Marrero, Laila Moujir, Lucia S. Andres, Nayely P. Montano, Liliana Araujo, and Javier G. Luis Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (cis)-1 (Z)-Benzylidene-5,5-dimethyl-3-tosyl-3,4,4a,5,7,8,9,-10b-octahydro-1H-chromeno[3,4-c]pyridin-10(2H)-one C28H31NO4S ÏàËÆ¶È:64% Tetrahedron 2012 68 2146-2154 2-(N-Allylaminomethyl)cinnamaldehydes as substrates for syntheses of aza-polycycles via intramolecular cycloaddition reactions Amita Mishra, Neeraj Rastogi, Sanjay Batra Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . compound IIS ÏàËÆ¶È:64% Journal of Pharmaceutical Sciences 1983 72 617-621 Synthesis, isolation, and characterization of two stereoisomeric ring sulfoxides of thioridazine Eric C. Juenge, Clyde E. Wells, Donald E. Green, Irene S. Forrest and James N. Shoolery Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . dendronobiloside C C27H44O12 ÏàËÆ¶È:62.9% Planta Medica 2002 68 723-729 New Alloaromadendrane,Cadinene and Cyclocopacamphane Type Sesquiterpene Derivatives and Bibenzyls from Dendrobium nobile Qinghua Ye,Weimin Zhao Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Taxuyunnanine Y ÏàËÆ¶È:62.9% Tetrahedron 2003 59 37-45 Novel taxoids from the Chinese yew Taxus yunnanensis Sheng-Hong Li, Hong-Jie Zhang, Xue-Mei Niu, Ping Yao, Han-Dong Sun, Harry H.S Fong Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . guan fu base S C24H29NO5 ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2008 Vol. 91 759 A New Diterpenoid and a New Diterpenoid Alkaloid from Aconitum coreanum Chun-Hua Yang, Xia-Chang Wang, Qing-Fa Tang, Wen-Ying Liu, and Jing-Han Liu Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . oblongifoliagarcinine B C22H24O3 ÏàËÆ¶È:62.5% Helvetica Chimica Acta 2008 Vol. 91 938 New Biphenyl Constituents from Garcinia oblongifolia Xu Wu, Chang-Qiang Ke, Yi-Ping Yang, and Yang Ye Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . Secotridentoquinone ÏàËÆ¶È:62.5% Journal of Natural Products 2009 72 214-217 Structure and Absolute Configuration of the Fungal Ansabenzoquinone Rhizopogone Martin Lang, Erhard Jagers,Kurt Polborn, and Wolfgang Steglich Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . pirolatin ÏàËÆ¶È:62.5% Chemical & Pharmaceutical Bulletin 2004 52(6) 714-717 Phenolic Glycosides from Pyrola japonica Ju Sun KIM,Sang Hee SHIM,Yong Nan XU,Sam Sik KANG,Kun Ho SON,Hyeun Wook CHANG,Hyun Pyo KIM,and KiHwan BAE Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . leiocarpin E ÏàËÆ¶È:62.5% Chinese Chemical Letters 2004 15 191-193 A Styrylpyrone Dimer from the Bark of Goniothalamus leiocarpus Qing MU , Yi Neng HE , Wei Dong TANG , Chao Ming LI , Li Guang LOU ,Han Dong SUN , Bin XU , Guo Xun YANG , Chang Qi HU Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . 3R,7E-9-butoxylmegastigma-3-ol-3-O-¦Â-D-glucopyranoside C23H40O7 ÏàËÆ¶È:62.5% Journal of Asian Natural Products Research 2008 10 1109-1115 Three novel compounds from the leaves of Smallanthus sonchifolius Ying-Kun Qiu, Ting-Guo Kang, De-Qiang Dou, Li Liang and Feng Dong Structure 13C NMR ̼Æ×Ä£Äâͼ |
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