| ²é¿´: 237 | »Ø¸´: 1 | |||
ever_lijuanר¼Ò¹ËÎÊ
|
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú-31 ÒÑÓÐ1È˲ÎÓë
|
|
18.77,55.99,56.36,56.58,61.50,67.10,69.72,70.11,70.45,70.68,72.62,97.72,109.60,113.65,113.74,118.81,124.17,124.95,143.20,148.60,150.52 ÈܼÁ£ºCDCl3 |
» ²ÂÄãϲ»¶
316Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
342Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
319Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
¡¾Çóµ÷¼Á¡¿085601²ÄÁϹ¤³Ìר˶ | ×Ü·Ö272 |
ÒѾÓÐ10È˻ظ´
26¿¼Ñе÷¼Á
ÒѾÓÐ3È˻ظ´
294·Ö080500²ÄÁÏ¿ÆÑ§Ó빤³ÌÇóµ÷¼Á
ÒѾÓÐ16È˻ظ´
µ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸Ö£´ó²ÄÁϹ¤³Ì290Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×Ò»¸ö£¬ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ8È˻ظ´
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
΢Æ×13C NMRÊý¾Ý¿â ²éδ֪»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
lifeliuyan
Ö÷¹ÜÇø³¤
![]()
![]()
![]()
![]()
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ever_lijuan: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-03-04 22:10:39
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
ever_lijuan: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2014-03-04 22:10:39
|
²éѯ½á¹û£º¹²²éµ½33¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 4-(3',4'-dimethoxyphenyl)-3-methoxy-6-(4''-methoxyphenyl)methylene-2H-pyran-2,5(6H)-dione C22H20O7 ÏàËÆ¶È:57.1% Australian Journal of Chemistry 1990 43 1497-1518 Pigments of Fungi. XV. An Efficient, Unambiguous Route to Unsymmetrically Substituted Dibenzyl Acyloins and Their Use in the Synthesis of Fungus Pigments of the Pulvinone and Grevillin Types M Gill, MJ Kiefel, DA Lally and A Ten Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . orobol 5,3'-di-O-methyl-8-C-glucoside C23H24O11 ÏàËÆ¶È:56.5% Phytochemistry 1999 52 141-145 Flavonoids from Maclura tinctoria H.N. El-Sohly, A. Joshi, X.-C. Li, S.A. Ross Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . haploperoside D C22H28O13 ÏàËÆ¶È:54.5% Chemistry of Natural Compounds 1985 21 25-32 COUMARIN GLYCOSIDES OF Haplophyllum perforatum. STRUCTURES OF HAPLOPEROSIDES C, D, AND E M. P. Yuldashev, E. Kh. Batirov,A. D. Bdovin, V. M. Malikov, and M. R. Yagudaev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . Erythribyssin C C22H24O5 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry Letters 2009 19 6745-6749 Cytotoxic and PTP1B inhibitory activities from Erythrina abyssinica Phi Hung Nguyen, Thi Van Thu Le, Phuong Thien Thuong, Trong Tuan Dao, Derek Tantoh Ndinteh, Joseph Tanyi Mbafor, Keon Wook Kang, Won Keun Oh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 7-O-(2-O-sinapoyl-¦Â‑D-glucopyranosyl)-6-methoxycoumarin C27H28O13 ÏàËÆ¶È:54.1% Planta Medica 2013 79 1558-1564 Chemical Constituents from the Roots and Stems of Erycibe obtusifolia and Their In Vitro Antiviral Activity Fan, Long; Wang, Ying; Liang, Ning; Huang, Xiao-Jun; Li, Man-Mei; Fan, Chun-Lin; Wu, Zhen-Long; Li, Yao-Lan; Ye, Wen-Cai: Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 8-hydroxydihydropalmatine ÏàËÆ¶È:52.3% Journal of Natural Products 2003 66 481-486 Palmatine and Berberine Isolation Artifacts Radek Marek, Pavlna Sečkov, Dagmar Hulov, Jaromr Marek, Ji Dostl, and Vladimr Sklen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . haploperoside C C24H30O14 ÏàËÆ¶È:52.3% Chemistry of Natural Compounds 1985 21 25-32 COUMARIN GLYCOSIDES OF Haplophyllum perforatum. STRUCTURES OF HAPLOPEROSIDES C, D, AND E M. P. Yuldashev, E. Kh. Batirov,A. D. Bdovin, V. M. Malikov, and M. R. Yagudaev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . ethyl 2(E)-3-(4-(3-((R)-2-((S)-1,2-dihydroxyethyl)-4-hydroxy-5-oxo-2,5-dihydrofuran-3-yloxy)-2-hydroxypropoxy)-3-methoxyphenyl)acrylate ÏàËÆ¶È:52.3% Molecules 2007 12 2533-2545 Synthesis of New L-Ascorbic Ferulic Acid Hybrids Anne Sophie Voisin-Chiret, Marc-Antoine Bazin, Jean-Charles Lancelot and Sylvain Rault Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 7,8-dihydro-8-hydroxypalmatine ÏàËÆ¶È:52.3% Phytochemistry 1999 50 279-281 A 7,8-dihydro-8-hydroxypalmatine from Enantia chlorantha Pascal Wafo, Barthelemy Nyasse, Catherine Fontaine Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 10-demethylxylopinine C20H23NO4 ÏàËÆ¶È:52.3% Journal of Natural Products 2010 73 115-122 Biotransformation of Phenolic Tetrahydroprotoberberines in Plant Cell Cultures Followed by LC-NMR, LC-MS, and LC-CD Kinuko Iwasa, Wenhua Cui, Teturo Takahashi, Yumi Nishiyama, Miyoko Kamigauchi, Junko Koyama, Atsuko Takeuchi, Masataka Moriyasu and Kazuyoshi Takeda Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 4-O-methylellagic acid 3-O-¦Á-L-rhamnopyranoside ÏàËÆ¶È:52.3% Natural Product Sciences 2007 13 160-163 An Ellagic Acid Rhamnoside from the Roots of Potentilla discolor with Protein Glycation and Rat Lens Aldose Reductase Inhibitory Activity Jang, Dae-Sik; Yoo, Nam-Hee; Kim, Jong-Min; Lee, Yun-Mi; Yoo, Jeong-Lim; Kim, Young-Sook; Kim, Jin-Sook Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 1b ÏàËÆ¶È:52.3% Phytochemistry 1993 33 1373-1375 Geranyl 6-O-¦Â-D-xylopyranosyl-¦Â-D-glucopyranoside isolated as an aroma precursor from tea leaves for oolong tea Wenfei Guo, Kanzo Sakata, Naoharu Watanabe, Ryuta Nakajima, Akihito Yagi, Kazuo Ina, Shaojun Luo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . Keteleeroside B C21H30O13 ÏàËÆ¶È:52.3% Zeitschrift f¨¹r Naturforschung B 2011 66b 733-739 Benzoic Acid Allopyranosides and Lignan Glycosides from the Twigs of Keteleeria evelyniana Wen Jun He, Zhao Hui Fu, Hong Jin Han, He Yan, Guang Zhi Zeng,Chang Jiu Jia, Hong Biao Chu, Yu Mei Zhang, and Ning Hua Tan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . foliachinenosides B2 C21H30O11 ÏàËÆ¶È:52.3% Heterocycles 2008 75 1435-1446 New Phenolic Glycosides from the Leaves of Salacia chinensis Seikou Nakamura, Yi Zhang, Tao Wang, Hisashi Matsuda, and Masayuki Yoshikawa Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . oxoglaucidaline C21H19NO6 ÏàËÆ¶È:52.3% Journal of Ethnopharmacology 2008 119 74-80 Cholinesterase inhibitory and anti-amnesic activity of alkaloids from Corydalis turtschaninovii Tran Manh Hung, MinKyun Na, Nguyen Tien Dat, Tran Minh Ngoc, UiJoung Youn, Hong Jin Kim, Byung-Sun Min, JongPill Lee, KiHwan Bae Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 16a C24H23NO3 ÏàËÆ¶È:52.3% European Journal of Organic Chemistry 2010 1798-1808 Regioselective Arylations of ¦Á-Amido Sulfones with Electron-Rich Arenes through Friedel¨CCrafts Alkylations Catalyzed by Ferric Chloride Hexahydrate: Synthesis of Unsymmetrical and Bis-Symmetrical Triarylmethanes Ponnaboina Thirupathi and Sung Soo Kim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 1,4-dideoxy-1,4-{(S)-[(2S,3S,4S,5R,6S)-2,4-O-isopropylidene-5,6,7-tri-O-methoxymethyl-3-(sulfooxy)heptyl]episulfoniumylidene}-D-arabinitol inner salt C21H40O15S2 ÏàËÆ¶È:52.3% Bioorganic & Medicinal Chemistry 2012 20 6321-6334 Role of the side chain stereochemistry in the ¦Á-glucosidase inhibitory activity of kotalanol, a potent natural ¦Á-glucosidase inhibitor. Part 2 Genzoh Tanabe, Kanjyun Matsuoka, Masahiro Yoshinaga, Weijia Xie, Nozomi Tsutsui, Mumen F. A. Amer, Shinya Nakamura, Isao Nakanishi, Xiaoming Wu, Masayuki Yoshikawa, Osamu Muraoka Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . 3-methoxyphenol 1-O-¦Á-L-rhamnopyranosyl-(1¡ú6)-O-¦Â-D-glucopyranoside C19H28O11 ÏàËÆ¶È:52.3% Molecules 2013 18 1255-1261 A New Phenolic Glycoside from Chamaecyparis obtusa var. breviramea f. crippsii Yu-Mei Zhang, Jian Xu, Lin Xiao, Guang-Zhi Zeng, Zhang-Hua Sun and Ning-Hua Tan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . tetrabenzo[b,e,q,t]-30-couronne-10 C36H40O10 ÏàËÆ¶È:52.3% Canadian Journal of Chemistry 1994 72 1218-1224 Solid state and solution stereochemistry of crown ethers and models. ortho-Dimethoxydiphenyl ether and related dibenzo-15-crown-5 and tetrabenzo-30-crown-10 ethers as studied by X-ray crystallography and 1H and 13C NMR spectroscopy G. W. Buchanan, A. Rodrigue, K. Bourque, A. C. Chiverton, I. R. Castleden, S. Fortier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . illoliganoside B C21H32O12 ÏàËÆ¶È:52.3% Carbohydrate Research 2011 346 1165-1168 Four new phenolic diglycosides from the roots of Illicium oligandrum Shuang-Gang Ma, Wen-Zhao Tang, Shi-Shan Yu, Xiao-Guang Chen, Yang Liu, Wen-Jie Wang, Jing Qu, Song Xu, Jin-Hong Ren, Yong Li, Hai-Ning L¨¹ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-03-04 21:56:33














»Ø¸´´ËÂ¥