| ²é¿´: 289 | »Ø¸´: 3 | |||
hylovexf001Òø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú2203ÒÑÓÐ1È˲ÎÓë
|
| ÈܼÁ£ºAcetone-d6 27.4,66.5,81.6,96.1,101.1,106.2,107.0,112.3,129.9,133.0,145.8,154.6,154.8,158.3,163.9,170.8 |
» ²ÂÄãϲ»¶
Ͷ¸åElsevierµÄNeoplasiaÔÓÖ¾£¬µ½×îºóÑ¡publishing optionsÊ±Ò³Ãæ¿Õ°×£¬²»ÄÜÍê³ÉͶ¸å
ÒѾÓÐ22È˻ظ´
ÉêÇë26²©Ê¿
ÒѾÓÐ5È˻ظ´
Ö°³ÆÆÀÉóû¹ý£¬Çó°²Î¿
ÒѾÓÐ22È˻ظ´
À¬»øÆÆ¶þ±¾Ö°³ÆÆÀÉó±ê×¼
ÒѾÓÐ15È˻ظ´
ESTͶ¸å״̬ÎÊÌâ
ÒѾÓÐ7È˻ظ´
±ÏÒµºóµ±¸¨µ¼Ô±ÁË£¬ÌìÌì¸÷ÖÖѧÉú³¬·³
ÒѾÓÐ4È˻ظ´
ƸU VÈÈÈÛ½ºÑо¿ÈËÔ±
ÒѾÓÐ10È˻ظ´
ÇóÖúÎÄÏ×
ÒѾÓÐ3È˻ظ´
Ͷ¸å·µÐÞºóÊÕµ½ÕâÑùµÄ»Ø¸´£¬»¹ÓÐÏ£ÍûÂð
ÒѾÓÐ8È˻ظ´
ÈýÎÞ²úÆ·»¹Óлú»áÂð
ÒѾÓÐ6È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú лл´ó¼Ò
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»~~
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл¸÷λ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»¸÷λ´óÉñ
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏߵȡ¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»´óÉñ£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý3¸ö
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
Àî×ÊÀÚ
Òø³æ (СÓÐÃûÆø)
- Ó¦Öú: 6 (Ó×¶ùÔ°)
- ½ð±Ò: 297.3
- ºì»¨: 2
- Ìû×Ó: 164
- ÔÚÏß: 27.7Сʱ
- ³æºÅ: 1776508
- ×¢²á: 2012-04-24
- ÐÔ±ð: GG
- רҵ: ÖÐҩѧÆäËû¿ÆÑ§ÎÊÌâ
2Â¥2014-10-21 14:39:13
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 47761.9
- ºì»¨: 52
- Ìû×Ó: 6670
- ÔÚÏß: 546.2Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hylovexf001: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡ 2014-10-21 15:52:28
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
hylovexf001: ½ð±Ò+10, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл£¡ 2014-10-21 15:52:28
|
1 . (-)-¶ù²èËØ(2S,3R) ÏàËÆ¶È:62.5% Chinese Journal of Medicinal Chemistry 2001 11 51-62 Study Progress on the Chiral Separation YIN Guo, LIU Zhen-hua, ZENG Shan-shan, ZHU Guo-hong Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 26a C31H28O14 ÏàËÆ¶È:56.2% Chemical & Pharmaceutical Bulletin 1989 37 3255-3263 Tannins and Related Compounds. XC. : 8-C-Ascorbyl (-)-Epigallocatechin 3-O-Gallate and Novel Dimeric Flavan -3-ols, Oolonghomobisflavans A and B, from Oolong Tea. (13) Fumio HASHIMOTO,Gen-ichiro NONAKA and Itsuo NISHIOKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (+)-gallocatechin ÏàËÆ¶È:56.2% Journal of the Chinese Chemical Society 1995 42 77-82 Chemical Constituents from the Roots of Zizyphus jujuba Mill. var. spinosa(¢ñ) Àîˮʢ(Shoei-Sheng Lee);ÍõÕý˜Ð(Jeng-Shu Wang);ê?‚Ñ©(Karin Chiung-Sheue Chen) Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 4',5,7-tri-hidroxi-6-metoxifavona ÏàËÆ¶È:56.2% Qu¨ªmica Nova 2010 33 1877-1881 Flavonoids and other substances from Lippia sidoides and their antioxidant activities Almeida, Macia Cleane S. de; Alves, Leonardo A.; Souza, Luciana Greg¨®rio da S.; Machado, Luciana L.; Matos, Marcos C. de; Oliveira, Maria Conceição F. de; Lemos, Telma L. G.; Braz-Filho, Raimundo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . oroxylin A C16H12O5 ÏàËÆ¶È:56.2% Natural Product Research and Development 2014 26 212-214 Five Phenols from Kalimeris indica JI Peng, WANG Guo-kai*, LIU Jin-song, LUO Zheng-hui, LIU Ji-kai, WANG Gang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . phyllocoumarin ÏàËÆ¶È:52.9% Phytochemistry 1989 28 2477-2481 Flavanocoumarins and flavanophenylpropanoids from Phyllocladus trichomanoides Lai Yeap Foo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 11b C54H50O26 ÏàËÆ¶È:52.9% Tetrahedron 2011 67 2051-2059 Production and degradation mechanism of theacitrin C, a black tea pigment derived from epigallocatechin-3-O-gallate via a bicyclo[3.2.1]octane-type intermediate Yosuke Matsuo, Yan Li, Sayaka Watarumi, Takashi Tanaka, Isao Kouno Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . compound 15 ÏàËÆ¶È:52.9% Magnetic Resonance in Chemistry 1989 27 1181-1183 Carbon-13 NMR chemical shift assignment of neoflavonoids Giuliano Delle Monache, Irene Messana, Bruno Botta and Eszter G¨¢cs-Baitz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . methyl 5-acetoxymethanol-7-hydroxy-2,2-dimethyl-2H-1-chromene-6-carboxylate C14H16O4 ÏàËÆ¶È:50% Phytochemistry 2005 66 573-579 Chromenes of polyketide origin from Peperomia villipetiola Karina J. Malquichagua Salazar, Guillermo E. Delgado Paredes,Luis Ripalda Lluncor, Maria Claudia Max Young, Massuo Jorge Kato Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . (-) gallocatechin ÏàËÆ¶È:50% Acta Botanica Yunnanica 1995 17(2) 204-208 CHEMICAL CONSTITUENTS OF "ECOLOGICAL TEA" FROM YUNNAN ZHANG Wen-Jie, LIU Yu-Qing, LI Xing-Cong, YANG Choug ken Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 28a C31H28O14 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1989 37 3255-3263 Tannins and Related Compounds. XC. : 8-C-Ascorbyl (-)-Epigallocatechin 3-O-Gallate and Novel Dimeric Flavan -3-ols, Oolonghomobisflavans A and B, from Oolong Tea. (18) Fumio HASHIMOTO,Gen-ichiro NONAKA and Itsuo NISHIOKA Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . compound 3 ÏàËÆ¶È:50% Chemistry of Natural Compounds 1997 33 417-437 1H AND 13C NMR SPECTROSCOPY IN THE STUDY OF FLAVAN-3-OLS, PROANTHOCYANIDINS, AND THEIR DERIVATIVES Ill. 13C NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY OF FLAVAN-3-OLS AND PROANTHOCYANIDINS A. D. Vdovin, Z. A. Kuliev, and N. D. Abdullaev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 62 ÏàËÆ¶È:50% Chemistry of Natural Compounds 1997 33 417-437 1H AND 13C NMR SPECTROSCOPY IN THE STUDY OF FLAVAN-3-OLS, PROANTHOCYANIDINS, AND THEIR DERIVATIVES Ill. 13C NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY OF FLAVAN-3-OLS AND PROANTHOCYANIDINS A. D. Vdovin, Z. A. Kuliev, and N. D. Abdullaev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . methyldactyloidin ÏàËÆ¶È:50% Natural Product Research 1999 14 141-146 Demethyldactyloidin and Other Constituents in Myristica Ceylanica H. M. T. B. Herath; Wimal Padmasiri Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . gallocatechin ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2007 32 593-596 Study on flavanols from Glochidion hirsutum YANG Jin, YANG Xiaodong, YANG Shu, ZHAO Jingfeng, LI Liang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 4'-hydroxy-7-methoxy-flavan-3-ol C16H16O4 ÏàËÆ¶È:50% Phytochemistry 2000 54 891-896 Minor phenolics from Crinum bulbispermum bulbs M.A. Ramadan, M.S. Kamel, K. Ohtani, R. Kasai, K. Yamasaki Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . dihydroresveratrol ÏàËÆ¶È:50% Phytochemistry 1999 52 1365-1369 Bibenzyl derivatives from the orchid Dendrobium amoenum P.L Majumder, S. Guha, S. Sen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . columbianetin acetate ÏàËÆ¶È:50% Phytochemistry 1998 48 637-641 Flavonoids and bioactive coumarins of Tordylium apulum Constantinos Kofinas, Ioanna Chinou, Anargiros Loukis, Catherine Harvala, Marc Maillard, Kurt Hostettmann Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . (+)-gallocatechin ÏàËÆ¶È:50% Natural Product Sciences 2005 11 119-122 In vitro Free Radical Scavenging and Hepatoprotective Compound from Sanguisorbae Radix An, Ren-Bo; Tian, Yu-Hua; Oh, Hyun-Cheol; Kim, Youn-Chul Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 20 . pinnatin ÏàËÆ¶È:50% Phytochemistry 1994 37 1363-1366 A diterpenoid from roots of Gelonium multiflorum Binayak Das, Ajit Kumar Chakravarty, Kazuo Masuda, Hideki Suzuki, Hiroyuki Ageta Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 21 . (-)-puerol B ÏàËÆ¶È:50% Phytochemistry 1993 33 1207-1210 But-2-enolides from Pueraria lobata and revised structures of puerosides A, B and sophoroside A Toshihiro Nohara, Junei Kinjo, Junichi Furusawa, Yusuke Sakai, Mutsumi Inoue, Yoshiaki Shirataki, Yayoi Ishibashi (Nee Tagaya), Ichiro Yokoe, Manki Komatsu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 22 . (+)-gallocatechin ÏàËÆ¶È:50% Korean Journal of Pharmacognosy 1998 29(3) 217-224 Phenolic Compounds from the Stem Bark of Cornus walteri Wanger Choi, Woo-Hoi; Park, Woong-Yang; Hwang, Bang-Yeon; Oh, Gap-Jin; Kang, Shin-Jung; Lee, Kyong-Soon; Ro, Jai-Seup Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 23 . compound 2a C17H14O7 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 1987 35 4429-4435 Flavonoids from Andrographis paniculata MASANORI KUROYANAGI,MAKOTO SATO,AKIRA UENO and KOUZABURO NISHI Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 24 . epigallocatechin ÏàËÆ¶È:50% China Journal of Chinese Materia Medica 2010 35 2420-2423 Chemical constituents of Desmodium sambuense LI Chuankuan; ZHANG Qianjun; HUANG Zhongbi; CHEN Qing; YAO Rongjun Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 25 . Compound 2c C32H28O14 ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2002 40 693-704 2D NMR analysis for unambiguous structural elucidation of phenolic compounds formed through reaction between (+)-catechin and glyoxylic acid Nour-Eddine Es-Safi, Christine Le Guernev¨¦, V¨¦ronique Cheynier and Michel Moutounet Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 26 . Compound 2c C32H28O14 ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2002 40 693-704 2D NMR analysis for unambiguous structural elucidation of phenolic compounds formed through reaction between (+)-catechin and glyoxylic acid Nour-Eddine Es-Safi, Christine Le Guernev¨¦, V¨¦ronique Cheynier and Michel Moutounet Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 27 . 5-ôÇ»ù-8-¦Ã,¦Ã-ÒìÎìÏ©»ù-6'',6''-¶þ¼×»ù-ßÁà«(6,7: 3'',2'')É«Ôͪ C19H20O4 ÏàËÆ¶È:50% Chinese Traditional and Herbal Drugs 2009 40 865-868 Ðâëǧ½ï°Î¸ùµÄ»¯Ñ§³É·ÖÑо¿ ÕÅÑ©;ËÎÆôʾ Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 28 . (-)-gallocatechin ÏàËÆ¶È:50% Chinese Journal of Natural Medicines 2009 7 111-114 Chemical Constituents from the Leaves of Camellia assamica var. kucha Chang et Wang XU Jie-Kun; ZHANG Wei-Ku; HIROSHI Kurihara; YAO Xin-Sheng Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 29 . compound 18 C13H10O4 ÏàËÆ¶È:50% Tetrahedron Letters 2001 42 3283-3286 An unexpected ring-opening of a 2-pyrone ring at low temperatures. A mild and expeditious synthesis of novel coumarins Ossama Saleh Darwish, Kirsten A Granum, Quang Tan, Richard P Hsung Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 30 . 2-amino-4-(1,2-O-isopropylidene-¦Á-D-glycero-tetr-3-enofuranos-4-yl) pyrimidine-5-carbonitrile C12H12N4O3 ÏàËÆ¶È:50% Zeitschrift f¨¹r Naturforschung B 2006 61 292-300 Dimethylaminomethylene-a-D-xylo-hept-5-ulofuranurononitrile as Building Block in the Synthesis of 'Reversed' C-Nucleoside Analogues I. A. Hashmi, H. Feist, M. Michalik, H. Reinke, and K. Peseke Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

3Â¥2014-10-21 14:56:01
hylovexf001
Òø³æ (СÓÐÃûÆø)
- Ó¦Öú: 2 (Ó×¶ùÔ°)
- ½ð±Ò: 933.5
- Ìû×Ó: 95
- ÔÚÏß: 84.2Сʱ
- ³æºÅ: 955558
- ×¢²á: 2010-02-15
- רҵ: ·ÖÎö»¯Ñ§
4Â¥2014-10-21 15:54:49













»Ø¸´´ËÂ¥