| ²é¿´: 952 | »Ø¸´: 4 | ||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | ||
·½°¬Õýгæ (СÓÐÃûÆø)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý²éѯ
|
|
|
dmsoÈܽâ ΢Æ×Êý¾Ý£º 61.24,70.62,71.96,72.38,73.09,92.22 [ Last edited by ·½°¬Õý on 2013-3-30 at 19:40 ] |
» ²ÂÄãϲ»¶
ÓжàÉÙÈËÊǽñÌì²éϵͳ֪µÀ½á¹ûµÄ£¿
ÒѾÓÐ18È˻ظ´
»ù½ðϵͳʲôÄÚÈÝҲûÓÐ
ÒѾÓÐ6È˻ظ´
¹ú×ÔÈ»ÃæÉϸ´ÅÌ~»¶ÓÌÖÂÛ
ÒѾÓÐ12È˻ظ´
Ϊʲô×ÊÖúÊý¸÷´ó¸ßУ¶¼´´Ð¸ߣ¬×Ô¼ºÉêÇëÔõô¾ÍÕâôÄÑ
ÒѾÓÐ9È˻ظ´
ÊÛSCIÒ»ÇøÎÄÕ£¬ÎÒ:8O5.5.1.O5.4,¿ÆÄ¿È«,¿ÉÙ¤¼±
ÒѾÓÐ3È˻ظ´
ÄÄλ¸ßÈËÖÐÁË£¬°Ñ²éѯµ½µÄ½ØÍ¼Ìù³öÀ´ÈÃÎÒ¿´¿´£¬ÈÃÎÒ³¤³¤¼ûʶ
ÒѾÓÐ6È˻ظ´
ÊÛSCIÎÄÕ£¬ÎÒ:8O5.5.1.O.54,¿ÆÄ¿ÆëÈ«,¿É+¼±
ÒѾÓÐ4È˻ظ´
ÃæÉϺÏ×÷µ¥Î»¸ÇÕÂ
ÒѾÓÐ5È˻ظ´
µ¼Ê¦Í²ۣºÎÒÔõô̯ÉÏÁËÕâô¸ö¼«Æ·Ñо¿Éú£¡
ÒѾÓÐ7È˻ظ´
ÉêÇëɾ³ý±¾Ìû
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ
ÒѾÓÐ3È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ£¡¼±Çó£¡
ÒѾÓÐ6È˻ظ´
10½ð±ÒÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
wm0629
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 341 (´óѧÉú)
- ½ð±Ò: 6381.8
- ºì»¨: 3
- Ìû×Ó: 1962
- ÔÚÏß: 77.9Сʱ
- ³æºÅ: 2217415
- ×¢²á: 2013-01-01
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÅÚÖÆ

4Â¥2013-03-31 16:00:26
wm0629
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 341 (´óѧÉú)
- ½ð±Ò: 6381.8
- ºì»¨: 3
- Ìû×Ó: 1962
- ÔÚÏß: 77.9Сʱ
- ³æºÅ: 2217415
- ×¢²á: 2013-01-01
- ÐÔ±ð: GG
- רҵ: ÖÐÒ©ÅÚÖÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·½°¬Õý: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ºÜ¸Ðл 2013-03-31 14:36:50
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
·½°¬Õý: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, ºÜ¸Ðл 2013-03-31 14:36:50
|
1 . ¦Á-D-Glucopyranose ÏàËÆ¶È:100% Magnetic Resonance in Chemistry 2003 41 1015-1020 Combined 1H, 13C and 11B NMR and mass spectral assignments of boronate complexes of D-(+)-glucose, D-(+)-mannose, methyl--D-glucopyranoside, methyl-¦Â-D-galactopyranoside and methyl--D-mannopyranoside Reem Smoum, Abraham Rubinstein and Morris Srebnik Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . ¦Á-ÆÏÌÑÌÇ ÏàËÆ¶È:100% Modern Chinese Medicine 2007 9(8) 10-11 Studies on the chemical Con stitun ts from Isodon Se rra (Maxim.) Kudo Liu Jinxiu, Gao Huimin, Wang Zhimin, Wang Weihao, Fu Xuetao Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . ¦Á-D-glucopyranosyl-¦Á-D-glucopyranoside ÏàËÆ¶È:100% Natural Product Research and Development 2008 20 60-62 Chemical Constituents from the Defatted Seeds of Linum usitatissimum L. SHI Gao-feng; SUN Hao-ran;ZHAO Yan-fang; CHEN Xue-fu; QI Zhi-guo Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . ¦Á-D-glucose ÏàËÆ¶È:100% Acta Chimica Sinica 1983 41 149-152 STUDIES ON THE CHEMICAL CONSTITUENTS OF BRUCEA JAVANICA II. BRUCEIN E-GLUCOPYRANOSIDE ZHANG JIN-SHENG; LIN LONG-ZE; OHEN ZHONG-LIANGXU REN-SHENG; SUN XIAN-YTJ Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¶þÌÇB[¦Á-D-glc-¦Á-D-glc(1¡úl)] C12H22O11 ÏàËÆ¶È:83.3% Chinese Traditional and Herbal Drugs 2004 35 493-495 È˹¤Ó¼³æ²Ý»¯Ñ§³É·ÖÑо¿ Íõ¸Õ,Âé±ø¼Ì,Áõ¼ª¿ª Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . methyl ¦Á-D-glucopyranoside ÏàËÆ¶È:71.4% Bulletin of the Chemical Society of Japan 1983 56 542-544 Chemical Studies on the Mistletoe. V. The Structure of Taxillusin, a New Flavonoid Glycoside Isolated from Taxillus kaempferi Atsushi Sakurai, Yasuaki Okumura Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . C-glucosyl moiety ÏàËÆ¶È:66.6% Phytochemistry 1989 28 299-301 8-C-glucosylscutellarein 6,7-dimethyl ether and its 2¡å-O-apioside from Abrus precatorius Kenneth R. Markham,James W. Wallace,Y.Niranjan Babut,V.Krishna Murty,M.Gopala Rao Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . D-Mannose ÏàËÆ¶È:66.6% Magnetic Resonance in Chemistry 2003 41 1015-1020 Combined 1H, 13C and 11B NMR and mass spectral assignments of boronate complexes of D-(+)-glucose, D-(+)-mannose, methyl--D-glucopyranoside, methyl-¦Â-D-galactopyranoside and methyl--D-mannopyranoside Reem Smoum, Abraham Rubinstein and Morris Srebnik Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . D-1-O-¼×»ù¼¡´¼ ÏàËÆ¶È:57.1% China Journal of Chinese Materia Medica 2006 31 1643-1645 º¬Ðß²ÝË®ÈÜÐԳɷֵÄÑо¿ Ô¬ ¿À , ÂÀ½àÀö, ÒóÃ÷ÎÄ Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Hexa-6-O-methyl (C17H32O5)6 ÏàËÆ¶È:57.1% Helvetica Chimica Acta 1978 61 2190-2218 Cyclodextrin chemistry. Selective modification of all primary hydroxyl groups of - and ¦Â-cyclodextrins Joshua Boger, Richard J. Corcoran and Jean-Marie Lehn Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . D-3-O-methyl chiroinositol C7H14O6 ÏàËÆ¶È:57.1% Phytochemistry 1988 27 3990-3991 Ethyl brevifolin carboxylate and other constituents from Acer oblongum leaves Nazneen Parveen,Nizam U. Khan,T. Inoue,M. Sakurai Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-O-methylinsitol ÏàËÆ¶È:57.1% China Journal of Chinese Materia Medica 2010 35 607-609 Chemical constituents in Flos Sophorae Carbonisatus LI Raorao*; WANG Caifang; LEI Peilin; HUANG Lanlan; YUAN Sitong Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . N,N'-Bis(2,3,4,6-tetra-O-acetyl-¦Â-D-glucopyranosylguanidinium chloride-H(+) C29H42N3O18 ÏàËÆ¶È:57.1% Magnetic Resonance in Chemistry 2001 39 283-287 NMR studies of the conformational behaviour and tautomerism of bis-and tris-saccharidoguanidines G¨¢bor T¨®th, Tam¨¢s G¨¢ti, Istv¨¢n Pint¨¦r, J¨®zsef Kov¨¢cs and Rainer Haessner Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 2 ÏàËÆ¶È:57.1% Chinese Traditional and Herbal Drugs 2010 41 204-206 ½ðÌúËø»¯Ñ§³É·ÖÑо¿ ³Â»ª¹ú; ÀîÃ÷; ¹¨Ð¡¼û; ÖÜÐÀ; ÌïÔ° Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . ¦Ä-3-O-¼×»ù¼¡´¼ ÏàËÆ¶È:57.1% Chinese Traditional and Herbal Drugs 2010 41 707-709 ´Ì»±»¨µÄ»¯Ñ§³É·ÖÑо¿ Û³³¤Óà;³õÕýÔÆ;ÍõÌìÃô;µÔÑÓ¾ý;¿µÍ¢¹ú Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-03-31 14:06:28
·½°¬Õý
гæ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 64.6
- Ìû×Ó: 51
- ÔÚÏß: 14.6Сʱ
- ³æºÅ: 1236857
- ×¢²á: 2011-03-17
- רҵ: ÉúÎﻯѧ
3Â¥2013-03-31 14:37:30
·½°¬Õý
гæ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 64.6
- Ìû×Ó: 51
- ÔÚÏß: 14.6Сʱ
- ³æºÅ: 1236857
- ×¢²á: 2011-03-17
- רҵ: ÉúÎﻯѧ
5Â¥2013-03-31 19:11:01









»Ø¸´´ËÂ¥