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shooter652: ½ð±Ò+8, ¡ïÓаïÖú 2014-06-17 10:17:29
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shooter652: ½ð±Ò+8, ¡ïÓаïÖú 2014-06-17 10:17:29
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²éѯ½á¹û£º¹²²éµ½1174¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . (20R,22R)-20,22,25-trihydroxy-2 ¦Â,3 ¦Â-(isopropylidenedioxy)-5¦Â-cholest-8(14)-en-6-one ÏàËÆ¶È:66.6% Russian Journal of Organic Chemistry 2010 46 1735-1740 ¦¤8(14)-14¦Á-deoxy- and 14¦Á-deoxy-14¦Á-hydroperoxyecdysteroids A. Sh. Ibragimova, N. A. Ves¡¯kina, I. V. Galyautdinov and V. N. Odinokov Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . cumingianol A C32H54O6 ÏàËÆ¶È:65.6% Phytochemistry 2011 72 2205-2211 Triterpenes and a triterpene glucoside from Dysoxylum cumingianum Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3¦Á,12¦Á,16¦Â-Trihydroxy-5¦Â-cholan-24-oic acid C24H40O5 ÏàËÆ¶È:64.2% Steroids 2010 75 506-512 Synthesis, aggregation behavior and cholesterol solubilization studies of 16-epi-pythocholic acid (3¦Á,12¦Á,16¦Â-trihydroxy-5¦Â-cholan-24-oic acid) Nonappa, Uday Maitra Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3,20,24,25-tetrahydroxydammarane C30H54O4 ÏàËÆ¶È:63.3% Phytochemistry 2004 65 2173-2176 Insect antifeedant compounds from Nothofagus dombeyi and N. pumilio Odile Thoison, Thierry S¨¦venet, Hermann M. Niemeyer, Graeme B. Russell Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . panicualtin D C32H52O7 ÏàËÆ¶È:63.3% Journal of the Indian Chemical Society 1999 76 575-581 Study of the stereochemistry of new tetranortriterpenoids isolated from root-wood of Chisocheton paniculatus Hiern(Meliaceae) R.D.Yadav,J.C.S.Kataky and R.K.Mathur Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . Cumingianol B C32H54O6 ÏàËÆ¶È:62.5% Phytochemistry 2011 72 2205-2211 Triterpenes and a triterpene glucoside from Dysoxylum cumingianum Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Cumingianol C C32H52O5 ÏàËÆ¶È:62.5% Phytochemistry 2011 72 2205-2211 Triterpenes and a triterpene glucoside from Dysoxylum cumingianum Shin-ichiro Kurimoto, Yoshiki Kashiwada, Kuo-Hsiung Lee, Yoshihisa Takaishi Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . paniculatin-D C32H52O7 ÏàËÆ¶È:62.5% Indian Journal of Chemistry Section B 1999 38B 1359-1363 New protolimonoids and limonoids art I-isolation,structure elucidation of new protolimonoids and limonoid from the root wood of Chisocheton paniculatus Hiern(Meliaceae)R D Yadav, J C S Kataky&R K mathur Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Kadpolysperin C C32H50O5 ÏàËÆ¶È:62.5% Tetrahedron 2012 68 4820-4829 Kadpolysperins A¨CN, lanostane triterpene acids possessing rich structure types from Kadsura polysperma Ke Dong, Jian-Xin Pu, Xue Du, Jia Su, Xiao-Nian Li, Jian-Hong Yang, Wei Zhao, Yan Li, Han-Dong Sun Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . sugikurojin C C40H56O4 ÏàËÆ¶È:62.0% Chemical & Pharmaceutical Bulletin 2004 52(3) 354-358 A New Abietane and Two Dimeric Abietane Diterpenes from the Black Heartwood of Cryptomeria japonica Shigenobu ARIHARA,Akemi UMEYAMA, Shinya BANDO, Shinji IMOTO, Mikako ONO, Mayo TANI, and Kazuko YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . agladupol A C31H52O6 ÏàËÆ¶È:61.2% Journal of Natural Products 2007 70 1532-1535 Agladupols A¨CE, Triterpenoids from Aglaia duperreana Bo-Jun Xie, Sheng-Ping Yang, Hua-Dong Chen, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . petuniosterol B C28H48O7 ÏàËÆ¶È:60.7% Phytochemistry 1994 36 1307-1314 Ergostane glycosides from Petunia hybrida Kazushi Shingu, Hiroshi Fujii, Kouichi Mizuki, Ikuhiko Ueda, Shoji Yahara, Toshihiro Nohara Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 1¦Â,3¦Á,11¦Á,20-Tetraacetoxy-5¦Â-pregnane C29H44O8 ÏàËÆ¶È:60.7% Steroids 2011 76 1458-1464 Microwave assisted preparation of C(1)-C(11) oxygen-bridged pregnanes Lautaro D. Alvarez, Juan M. Sonego, Adriana S. Veleiro, Gerardo Burton Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 10 ÏàËÆ¶È:60.7% Steroids 1990 55 263-265 Studies of the synthesis of biomarkers. VII. Synthesis of 5¦Á-(17R,20R)-14,15-secocholestane Tong-Shuang Li, Yu-Lin Li, Xiao-Tian Liangt Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . compound IV ÏàËÆ¶È:60.7% Tetrahedron 1995 51 2009-2022 Structure determination of diacholestanes. Their geochemical significance Odette Sieskind, Jean P. Kintzinger, Bernard Metz, Pierre Albrecht Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . (¡À)-(1R*,9S*,10R*,11S*)-and (¡À)-(1R*,9R*,10S*,11R*)-10-hydroxy-12-methyl-1-nitrobicyclo[7.3.1]tridecan-13-one ÏàËÆ¶È:60.7% European Journal of Organic Chemistry 2011 2101-2110 A General, Diastereoselective Synthesis of Highly Functionalized Bicyclo[n.3.1]alkane Systems Based on an Anionic Domino Reaction of -Nitrocycloalkanones Giorgio Giorgi, Sonia Miranda, Miriam Ruiz, Jean Rodriguez, Pilar L¨®pez-Alvarado and J. Carlos Men¨¦ndez Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . sandorinic acid A C30H46O5 ÏàËÆ¶È:60% Journal of Natural Products 2001 64 1243-1245 New Multiflorane-Type Triterpenoid Acids from Sandoricum indicum Tadamitsu Tanaka,Takashi Koyano, Thaworn Kowithayakorn, Haruhiro Fujimoto, Emi Okuyama,Masahiko Hayashi,Kanki Komiyama, and Masami Ishibashi Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . Mesendanin Q C30H48O5 ÏàËÆ¶È:60% Helvetica Chimica Acta 2012 95 286-300 Triterpenoids from Melia toosendan Shi-Hui Dong, Xiu-Feng He, Lei Dong, Yan Wu, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ |

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art I-isolation,structure elucidation of new protolimonoids and limonoid from the root wood of Chisocheton paniculatus Hiern(Meliaceae)