| ²é¿´: 429 | »Ø¸´: 1 | ||
¼¾Ä©Ò²¼Åį½ð³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
Çó̼Æ× ÒÑÓÐ1È˲ÎÓë
|
| 62.84, 70.12,71.10, 71.35, 72.76,99.59, 111.60,180.68 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
0854Çóµ÷¼Á
ÒѾÓÐ21È˻ظ´
290Çóµ÷¼Á
ÒѾÓÐ25È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÉúÎïѧ326Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
294Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
085410-273Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
307ÖÐÒ½¿¼Ñе÷¼Á
ÒѾÓÐ6È˻ظ´
0831ÉúÒ½¹¤µÚÒ»ÂÖµ÷¼Áʧ°ÜÇóÖú
ÒѾÓÐ17È˻ظ´
291Çóµ÷¼Á
ÒѾÓÐ11È˻ظ´
297£¬¹¤¿Æµ÷¼Á?ºÓÄÏũҵ´óѧ±¾¿Æ
ÒѾÓÐ14È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¼¾Ä©Ò²¼Åį: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-10-26 10:19:59
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
¼¾Ä©Ò²¼Åį: ½ð±Ò+15, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2014-10-26 10:19:59
|
»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . ethyl ¦Á-D-glucopyranoside C8H16O6 ÏàËÆ¶È:75% Acta Botanica Yunnanica 2001 23(4) 527-530 Nitrogen - containing Compounds from Brachystemma calycinum CHENG Yong-Xian,ZHOU Jun, TENG Rong-Wei,TAN Ning-Hua Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ethyl-¦Á-D-galactopyranoside ÏàËÆ¶È:75% Natural Product Research 2002 16 283-290 Isolation and Structure Elucidation of Three Glycosides and a Long Chain Alcohol from Polianthes Tuberosa Linn. Khalid Mohammed Khan; Shahnaz Perveen; S. Abdul Majid Ayattollahi; Nikhat Saba; Adil Rashid; Sadiqa Firdous; Syed Moazzam Haider; Zia Ullah; Shagufta Rahat; Zarrar Khan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Á-ethyl-D-idosopyranoside C8H16O6 ÏàËÆ¶È:75% Chinese Traditional and Herbal Drugs 2009 40 850-852 Chemical constituents of Dai ethno-medicine Rhinacanthus nasutus YE Jie-ying; ZHANG Qing-zhi; RAO Gao-xiong Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Á-galactopyranoside ÏàËÆ¶È:75% Food Chemistry 2011 126 177-182 Enzymatic properties and transglycosylation of ¦Á-galactosidase from Penicillium oxalicum SO Masahiro Kurakake, Youichirou Moriyama, Riku Sunouchi, Shinya Nakatani Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . methyl ¦Á-D-galactopyranoside ÏàËÆ¶È:75% Canadian Journal of Chemistry 1980 58 2800-2804 Assignment of anomeric configuration and identification of carbohydrate residues by 13C nmr. 1. Galacto- and glucopyranosides and furanosides Ross C. Beier, Bradford P. Mundy, Gary A. Strobel Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . terminal galactose in raffinose ÏàËÆ¶È:75% Canadian Journal of Chemistry 1980 58 2800-2804 Assignment of anomeric configuration and identification of carbohydrate residues by 13C nmr. 1. Galacto- and glucopyranosides and furanosides Ross C. Beier, Bradford P. Mundy, Gary A. Strobel Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2014-10-26 10:15:30













»Ø¸´´ËÂ¥