| ²é¿´: 180 | »Ø¸´: 1 | ||
ygw198781гæ (³õÈëÎÄ̳)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý1¸ö
|
|
»¯ºÏÎï ÈܼÁ£ºDMSO NMR£º100HZ ̼Æ×Êý¾Ý£º 61.7,64.3,70.1,70.7,71.0,71.8,72.4,72.8,73.5,75.3,77.2,92.7,97.3 |
» ²ÂÄãϲ»¶
»úе¹¤³Ì264ѧ˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
264Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý3¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý1¸ö
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú2¸ö΢Æ×Êý¾Ý
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ£¡¼±Çó£¡
ÒѾÓÐ6È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
10½ð±ÒÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
yaolan123
½û³æ (Ö°Òµ×÷¼Ò)
- Ó¦Öú: 183 (¸ßÖÐÉú)
- ¹ó±ö: 0.255
- ½ð±Ò: 15027.2
- É¢½ð: 2847
- ºì»¨: 173
- ɳ·¢: 3
- Ìû×Ó: 3217
- ÔÚÏß: 486.8Сʱ
- ³æºÅ: 1352788
- ×¢²á: 2011-07-21
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
PSA: ½ð±Ò+2, лл 2013-05-29 17:59:33
ygw198781: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-05-30 08:39:44
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
PSA: ½ð±Ò+2, лл 2013-05-29 17:59:33
ygw198781: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-05-30 08:39:44
|
²éѯ½á¹û£º¹²²éµ½473¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . O-¦Á-D-galactopyranosyl-(1f3)-4-O-methyl-D-myo-inositol ÏàËÆ¶È:76.9% Journal of Natural Products 1997 60 749-751 Structure of Galactosylononitol Andreas Richter and Thomas Peterbauer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . compound2 ÏàËÆ¶È:76.9% Journal of Natural Products 1997 60 749-751 Structure of Galactosylononitol Andreas Richter and Thomas Peterbauer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . Mixture of ¦Á- and ¦Â-D-Galactose ÏàËÆ¶È:76.9% Phytochemistry 1998 49 1791-1795 Seven imidazole alkaloids from Lepidium sativum Ulrich H. Maier, Heidrun Gundlach, Meinhart H. Zenk Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . compound 11 ÏàËÆ¶È:76.9% Chinese Traditional and Herbal Drugs 2010 41 689-692 Chemical constituents from roots of Tinospora sagittata var. yunnanensis CHENG Chun-mei; DAI Yun; HUANG Xiang-zhong; ZHU Yun; DAI Jian-hui; LIU Xiao-fang; WANG Jiong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . glucose C6H12O6 ÏàËÆ¶È:76.9% Chinese Journal of Medicinal Chemistry 2011 21 220-225 Chemical constituents from dried fruits of Rubus chingii XIAO Hong-ming, ZU Ling-bo, LI Shi-ping, WANG Kai-jin, LI Ning* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 1 ÏàËÆ¶È:76.9% Russian Chemical Bulletin 1993 42 1742-1745 The structure and13C NMR spectra of mannitol oligo-¦Â-d-glucopyranosides isolated from the brown seaweed Chorda filum (L.) Lam A. I. Usov and A. O. Chizhov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 3-azido-3-deoxy-¦Á-D-glucopyranosyl-(1¡ú1')-¦Â-D-glucopyranoside C12H21N3O10 ÏàËÆ¶È:76.9% Tetrahedron 2013 69 816-825 Synthesis of 3,3¡ä-neotrehalosadiamine and related 1,1¡ä-aminodisaccharides using disarmed, armed, and superarmed building blocks Shazia Anjum, Natasha D. Vetter, Joseph E. Rubin, David R.J. Palmer Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . glu-mannitol ÏàËÆ¶È:76.9% Journal of Natural Products 2011 74 1477-1483 Iridoid and Phenylethanoid Glucosides from Veronica lavaudiana Rilka M. Taskova, Tetsuo Kokubun, Ken G. Ryan, Phil J. Garnock-Jones, and Søren R. Jensen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . inotodisaccharide ÏàËÆ¶È:76.9% Mycosystema 2010 29 897-910 Metabonomic analysis on production of antioxidant secondary metabolites by two geographically isolated strains of Inonotus obliquus in submerged cultures ZHENG Wei-Fa DAI Yu-Cheng SUN Jing ZHAO Yan-Xia MIAO Kang-Jie PAN Shen-Yuan ZHANG Mei-Mei WEI Jiang-Chun Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . 6-Tuliposide A C11H18O8 ÏàËÆ¶È:70.5% Phytochemistry 1995 38 1371-1373 Tuliposides from Alstroemeria revoluta Lars P. Christensen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . phillyraeoidin B C75H56O48 ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 1989 37 2030-2036 Tannins and Related Compounds. LXXXIII. : Isolation and Structures of Hydrolyzable Tannins, Phillyraeoidins A-E from Quercus phillyraeoides Gen-ichiro NONAKA,Shinji NAKAYAMA and Itsuo NISHIOKA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . tellimagrandin I ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 1988 36 2925-2933 13C Nuclear Magnetic Resonance Spectra of Hydrolyzable Tannins. II. : Tannins Forming Anomer Mixtures TSUTOMU HATANO,TAKASHI YOSHIDA,TETSURO SHINGU and TAKUO OKUDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . glucose core R ÏàËÆ¶È:69.2% Chemical & Pharmaceutical Bulletin 1988 36 2925-2933 13C Nuclear Magnetic Resonance Spectra of Hydrolyzable Tannins. II. : Tannins Forming Anomer Mixtures TSUTOMU HATANO,TAKASHI YOSHIDA,TETSURO SHINGU and TAKUO OKUDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 6-O-Monoester of Karatavikic acid and Sucrose ÏàËÆ¶È:69.2% Chemistry of Natural Compounds 1996 32 532-534 MODIFICATIONS BASED ON COUMARINS.I. SYNTHESIS OF MONOESTERS OF KARATAVIKIC AND GALBANIC ACIDS WITH SUCROSE A. F. Artamonova, K. A. Nusipbekova, F. S. Nigmat-llina,G. K. Nikonov, and B. Zh. Dzhienbaev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 6-O-Mouomethyl Ester of Galvanic acid and Sucrose ÏàËÆ¶È:69.2% Chemistry of Natural Compounds 1996 32 532-534 MODIFICATIONS BASED ON COUMARINS.I. SYNTHESIS OF MONOESTERS OF KARATAVIKIC AND GALBANIC ACIDS WITH SUCROSE A. F. Artamonova, K. A. Nusipbekova, F. S. Nigmat-llina,G. K. Nikonov, and B. Zh. Dzhienbaev Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . trans-O-Methylmarmesinic acid C27H38O15 ÏàËÆ¶È:69.2% Chemistry of Natural Compounds 1993 29 84-86 SYNTHESIS OF A MONOESTER OF SUCROSE WITH trans-O-METHYLMARMESINIC ACID A. F. Artamonov, F. S. Nigmatullina,and G. K. Nikonov Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . ¦Á-kolomiktriose C18H32O16 ÏàËÆ¶È:69.2% China Journal of Chinese Materia Medica 1992 17 420-421 Studies on Chemical Constituents of Actinidia kolomikta(Rupr.et Maxim.)Planch Li PINGYA, Lu AIPING, Ma Bingru and Weijunjie Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . conduritol A 1-O-¦Á-D-galactopyranoside C12H20O9 ÏàËÆ¶È:69.2% Phytochemistry 1998 47 1297-1301 Cyclitols and their glycosides from leaves of Marsdenia tomentosa Fumiko Abe, Tatsuo Yamauchi, Keiichi Honda, Nanao Hayashi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . 4-methylumbelliferyl cellobioside ÏàËÆ¶È:69.2% Bioorganic & Medicinal Chemistry Letters 2003 13 4039-4042 Glycosynthase-Catalysed syntheses at pH below neutrality Antonio Trincone, Assunta Giordano, Giuseppe Perugino, Mos¨¨ Rossi, Marco Moracci Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . Sucrose ÏàËÆ¶È:69.2% Natural Product Sciences 2010 16 32-38 Phytochemical Studies on Lonicerae Flos (1) - Isolation of Iridoid Glycosides and other Constituents Lee, Eun-Ju; Lee, Joo-Young; Kim, Ju-Sun; Kang, Sam-Sik Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-05-29 14:50:22














»Ø¸´´ËÂ¥