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vanvitamin: ½ð±Ò+5, ¡ï¡ï¡ïºÜÓаïÖú, ллÁË 2013-05-06 09:51:32
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Ã²ËÆ²»ÊÇ 1 . officinoside B C19H32O8 ÏàËÆ¶È:57.1% Chemical & Pharmaceutical Bulletin 2001 49(8) 974-978 Medicinal Flowers. IV.1) Marigold. (2): Structures of New Ionone and Sesquiterpene Glycosides from Egyptian Calendula officinalis Toshiyuki MARUKAMI, Akinobu KISHI, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Compound 2a C21H37O13N ÏàËÆ¶È:57.1% Bioorganic & Medicinal Chemistry Letters 1996 6 1123-1126 Synthesis of lactosamine derivatives using ¦Â--galactosidase from Bacillus circulans Shuichi Takayama, Makoto Shimazaki, Lei Qiao, Chi-Huey Wong Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . citronellol-1-O-¦Á-L-arabinofuranosyl-(1¡ú6)-¦Â-D-glucopyranoside C21H38O10 ÏàËÆ¶È:57.1% Molecules 2012 17 7629-7636 Terpene Glycosides from the Roots of Sanguisorba officinalis L. and Their Hemostatic Activities Wei Sun, Zi-Long Zhang, Xin Liu, Shuang Zhang, Lu He, Zhe Wang and Guang-Shu Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . (1S,2S,4R)-1,8-epoxy-p-methan-2-O-¦Â-D-glucopyranosyl(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:54.5% Pharmazie 2002 57 279-281 New isopimarane diterpene and new cineole type glucoside from Nepeta prattii Zhen-Fu Hou - Yong-Qiang Tu - Yu Li Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . (1R,2R,4S)-1,8-epoxy-p-methan-2-O-¦Â-D-glucopyranosyl-(1¡ú6)-¦Â-D-glucopyranoside ÏàËÆ¶È:54.5% Pharmazie 2002 57 279-281 New isopimarane diterpene and new cineole type glucoside from Nepeta prattii Zhen-Fu Hou - Yong-Qiang Tu - Yu Li Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . officinoside A C19H32O8 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 2001 49(8) 974-978 Medicinal Flowers. IV.1) Marigold. (2): Structures of New Ionone and Sesquiterpene Glycosides from Egyptian Calendula officinalis Toshiyuki MARUKAMI, Akinobu KISHI, and Masayuki YOSHIKAWA Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Ovatolactone 7-O-(6'-O-p-Hydroxybenzoyl)-¦Â-D-glucopyranoside C22H28O10 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 2001 49(6) 732-736 Studies on the Constituents of Catalpa Species. VI.Monoterpene Glycosides from the Fallen Leaves of Catalpa ovata G. DON Koichi MACHIDA, Megumi ANDO, Yasunori YAOITA, Rie KAKUDA, and Masao KIKUCHI Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . melia-ionoside A C19H36O8 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 1991 39 2529-2533 Phytochemical Studies on Meliaceous Plants. VII. The Structures of Two New Ionone Glucosides from Melia toosendan SIEB. et ZUCC. and a Novel Type of Selective Biooxidation by a Kind of Protease Tsutomu NAKANISHI,Mari KONISHI,Hiroko MURATA,Akira INADA,Atsushi FUJII,Naoki TANAKA and Takaji FUJIWARA Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . melia-ionoside A C19H36O8 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 1990 38 830-832 THE STRUCTURES OF TWO NEW IONONE GLUCOSIDES FROM MELIA TOOSENDAN AND A NOVEL TYPE OF SELECTIVE BIO-OXIDATION Tsutomu NAKANISHI,Mari KONISHI,Hiroko MURATA,Akira INADA,Atsushi FUJII,Naoki TANAKA and Takaji FUJIWARA Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . L-prolinium 4-(methylsulfinyl)butyl glucosinolate C17H32N2O12S3 ÏàËÆ¶È:52.3% Fitoterapia 2002 73 177-178 Glucosinolates from Cardaria draba Antoine F¨¦echard, Nicolas Fabre ,S¨¦bastien Hannedouche, Isabelle Fourast¨¦ Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 15¦Â-hydroxyisolineolon C21H32O6 ÏàËÆ¶È:52.3% Phytochemistry 2000 53 485-498 Steroidal glycosides from the aerial part of Asclepias incarnata Tsutomu Warashina, Tadataka Noro Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . Crassarine D C20H34O4 ÏàËÆ¶È:52.3% Marine drugs 2011 9 1955-1968 Bioactive Cembranoids from the Soft Coral Sinularia crassa Chih-Hua Chao,Kuei-Ju Chou,Chiung-Yao Huang,Zhi-Hong Wen,Chi-Hsin Hsu,Yang-Chang Wu,Chang-Feng Dai and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . sarcaglaboside G C21H30O9 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 2009 57 418-420 Three Novel Sesquiterpene Glycosides of Sarcandra glabra Xiao-ru Hu, Jun-shan Yang and Xu-dong Xu Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . Neolinustatinamide C17H31NO12 ÏàËÆ¶È:52.3% Phytochemical Analysis 2010 21 575-581 Synthesis and Characterisation of -Glycosyloxyamides Derived from Cyanogenic Glycosides Jandirk Sendker and Adolf Nahrstedt Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 2¦Á,5¦Á,7¦Â,9¦Á,13¦Á-pentahydroxy-10¦Â-acetoxytaxa-4(20),11-diene C22H34O7 ÏàËÆ¶È:52.3% Magnetic Resonance in Chemistry 2007 45 527-530 Structural determination of a new 2(3 ¡ú 20)abeotaxane with an unusual 13¦Â-substitution pattern and a new 6/8/6-ring taxane from Taxus cuspidata (pages 527¨C530) Changhong Huo, Xiaohui Su, Xing Li, Xiping Zhang, Cunfang Li, Yufang Wang, Qingwen Shi and Hiromasa Kiyota Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 3¦Â,19-Diacetoxy jesromotetrol C24H32O6 ÏàËÆ¶È:52.3% Phytochemistry 1985 24 3056-3058 Diterpenes from Palafoxia texana Antonio G. Gonz¨¢lez, Jos¨¦ J. Mendoza, Javier G. Luis, Angel G. Ravelo, Xorge A. Dom¨ªnguez, G. Cano Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 5 C20H36O4 ÏàËÆ¶È:52.3% Tetrahedron Letters 2002 43 4605-4608 Covilanone: a new rearranged labdane type diterpene J.M.L. Rodilla, M.I. Ismael, L.A. Silva, J.P. Ces¨¢rio Serrano, J.G. Urones, F. Sanz Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . (1S,2E,4S,6E,8S,11R,12R)-2,6-cembradiene-4,8,11,12-tetrol ÏàËÆ¶È:52.3% Acta Chemica Scandinavica 1986 40 123-134 Tobacco Chemistry. 69. Five New Labdanic Compounds from Tobacco. Wahlberg, Inger; Eklund, Ann-Marie; Nordfors, Kerstin; Vogt, Carmen; Enzell, Curt R.; Berg, Jan-Eric Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . Ovatolactone-7-O-(6'-O-p-hydroxybenzoyl)-¦Â-D-glucopyranoside C22H28O10 ÏàËÆ¶È:52.3% Chemical & Pharmaceutical Bulletin 2007 55 159-222 Naturally Occurring Iridoids. A Review, Part 1 Biswanath DINDA, Sudhan DEBNATH and Yoshihiro HARIGAYA Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . compound 17 C18H32O13 ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 1999 7 1549-1558 Bacteria targeted by human natural antibodies using ¦Á-gal conjugated receptor-specific glycopolymers Jun Li, Sima Zacharek, Xi Chen, Jianqiang Wang, Wei Zhang, Adam Janczuk, Peng George Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . 17¦ÂH-periplogenin C23H34O5 ÏàËÆ¶È:52.1% Phytochemistry 1988 27 2129-2133 Biotransformation of digitoxigenin by cell suspension cultures of Strophanthus gratus Tsutomu Furuya,Kiichiro Kawaguchi,Masao Hirotani Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . ent-2-oxo-15,16-dihydroxypima¦Á-8(14)-en-16-O-¦Â-glucopyranoside C26H42O8 ÏàËÆ¶È:50% Journal of Natural Products 2004 67 1517-1521 Novel Diterpenoids and Diterpenoid Glycosides from Siegesbeckia orientalis Ying Xiang, Hua Zhang, Cheng-Qi Fan, and Jian-Min Yue Structure 13C NMR ̼Æ×Ä£Äâͼ 23 . borapetosideA C26H34O12 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1985 33 4438-4444 Studies on the Constituents of the Stems of Tinospora tuberculata BEUMEE. II. New Diterpenoids, Borapetoside A and Borapetol A NAOMICHI FUKUDA,MICHIKO YONEMITSU,TAKEATSU KIMURA,SHIZUKO HACHIYAMA,KAZUMOTO MIYAHARA and TOSHIO KAWASAKI Structure 13C NMR ̼Æ×Ä£Äâͼ 24 . N-oxy-tuberostemonine C22H33NO5 ÏàËÆ¶È:50% Journal of Chinese Pharmaceutical Sciences 1999 8 1-7 Three New Alkaloids from the Roots of Stemona tuberosa Lour Lin Wenhan and Fu Hongzheng Structure 13C NMR ̼Æ×Ä£Äâͼ 25 . 13-Ethyl-11-methylene-18,19-dinor-17¦Á-pregn-4-en-20-yn-16¦Â,17-diol ÏàËÆ¶È:50% Steroids 2002 67 111-117 Base promoted air oxidation of 13¦Â-ethyl-11-methylenegon-4-en-17-one Federica Compostella, Diego Colombo, Emilia Modica, Antonio Scala, Lucio Toma, Bruna Bovio, Fiamma Ronchetti Structure 13C NMR ̼Æ×Ä£Äâͼ 26 . borapetoside A ÏàËÆ¶È:50% Phytochemistry 1989 28 2419-2422 A furanoid diterpene glucoside from Tinospora cordifolia R.K. Bhatt,B.K. Sabata Structure 13C NMR ̼Æ×Ä£Äâͼ 27 . 15-Hydroxytorreyol 10-O-(6-O-¦Â-D-apiofuranosyl)-¦Â-D-glucopyranoside C26H44O11 ÏàËÆ¶È:50% Helvetica Chimica Acta 2010 93 1407-1412 Glycosidic Constituents of Celastrus orbiculatus Yang Zhang, Chang-Heng Tan, Jun-Jie Tan, Pei-Ming Yang, Shan-Hao Jiang, Xiang Ni and Da-Yuan Zhu Structure 13C NMR ̼Æ×Ä£Äâͼ 28 . compound 2 C29H58NO13P ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 5305-5308 Synthesis of ¦Â-d-Galp-(1¡ú4)-¦Á-d-Manp methanephosphonate, a substrate analogue for the elongating ¦Á-d-mannosyl phosphate transferase in the Leishmania Vladimir S Borodkin, Michael A.J Ferguson, Andrei V Nikolaev Structure 13C NMR ̼Æ×Ä£Äâͼ 29 . daucosterol-6'-O-stearate ÏàËÆ¶È:50% Natural Product Research and Development 1996 8(1) 5-9 THE CONSTITUENTS FROM THE RHIZOMA OF ALTSMA ORIENTALIS (SAM) JUZEP. Cai Lining; Wang Hongshu; Cao Hongxing; Zhang Ruyi Structure 13C NMR ̼Æ×Ä£Äâͼ 30 . 1-tert-butyl2'-methyl5-iodo-2-oxo-1',5',6',7',8',8a'-hexahydro-2'H-spiro[indole-3,3'-indolizine]-1,2'(2H)-dicarboxylate C22H27IN2O5 ÏàËÆ¶È:50% Tetrahedron 2012 68 3103-3111 Skeletal diversity via Pd(0) catalysed three-component cascades of allene and halides or triflates with protected hydroxylamines and formamide Elghareeb E. Elboray, Chuanjun Gao, Ronald Grigg Structure 13C NMR ̼Æ×Ä£Äâͼ |

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