| ²é¿´: 578 | »Ø¸´: 2 | |||
| µ±Ç°Ö»ÏÔʾÂú×ãÖ¸¶¨Ìõ¼þµÄ»ØÌû£¬µã»÷ÕâÀï²é¿´±¾»°ÌâµÄËùÓлØÌû | |||
wangcong123ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
¹þ¹þ
|
[ÇóÖú]
»¯ºÏÎï½âÆ×---------- ̼Æ×-ÇóÏàËÆ¶È ÒÑÓÐ2È˲ÎÓë
|
||
| 18-5-1»¯ºÏÎï 13C NMR (126 MHz, dmso) ¦Ä 22.9,46.0,105.9,113.0,113.2,114.0,115.4,125.6,126.9,130.7,131.0,133.8,153.5,156.4,169.9,190.4 |
» ²ÂÄãϲ»¶
²ÄÁÏ¿ÆÑ§Ó빤³Ì320Çóµ÷¼Á£¬080500
ÒѾÓÐ9È˻ظ´
0703»¯Ñ§µ÷¼Á 348·Ö
ÒѾÓÐ10È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
Ò»Ö¾Ô¸211£¬0703»¯Ñ§305·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
284Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
²ÄÁϹ¤³Ìµ÷¼Á
ÒѾÓÐ5È˻ظ´
287Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
362Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ42È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
Çó½â̼Æ×£¬ÇâÆ×£¬´óÉñ°ïÖú£¬°æÖ÷Çó°ïÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×£¬Ð»Ð»À²£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл¸÷λ
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¡¸Ð¼¤£¡
ÒѾÓÐ3È˻ظ´
EPR½âÆ×ÎÊÌ⣬Çó
ÒѾÓÐ3È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
Ç×°®µÄ³æÓÑÃÇ ¹òÇó½âÆ×(̼Æ× ÇâÆ× ÖÊÆ×£© ¼±
ÒѾÓÐ19È˻ظ´
ÇâÆ×Ò»Ñù£¬Ì¼Æ×Óвî±ð£¬ÊÇÒ»¸öÎïÖÊÂð
ÒѾÓÐ24È˻ظ´
½ñÌìÔÙÇóÒ»´Î΢Æ× ³ê½ð20 ллÁË °´Õչ涨¸ñʽÕûÀíºÃ̼Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
Ò»°ã´ò̼Æ×»òÇâÆ×ÓÃʲôÈܼÁ
ÒѾÓÐ7È˻ظ´
ÊÇ·ñ´æÔÚÁ½ÖÖ»¯ºÏÎïÇâÆ×̼Æ×Ò»Ñù£¬µ«ÊÇdept-135ºÍdept-90µÄͼÊÇÕýºÃÏà·´µÄ£¿
ÒѾÓÐ6È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
NMR½âÆ×ÇóÖú£¡¼±£¡
ÒѾÓÐ12È˻ظ´
ÇóÖúÈý¸ö»¯ºÏÎ̼Æ×£©µÄ΢Æ×Êý¾Ý¿â¼ìË÷½á¹û£¨ÏàËÆ¶Èǰ20%£©
ÒѾÓÐ3È˻ظ´
Á½¸öÈýÝÆÀ໯ºÏÎï΢Æ×̼Æ×Êý¾Ý²éѯ
ÒѾÓÐ9È˻ظ´
ÇóÖúÇâÆ×̼Æ× ·ÖÎö~~~
ÒѾÓÐ4È˻ظ´
ºË´Å/ÖÊÆ×½âÆ×¸ßÊÖ°ïæ¿´¿´Õâ¸ö»¯ºÏÎï½á¹¹Ôõô½âÎö
ÒѾÓÐ12È˻ظ´
Çó¸ßÈ˽âÆ×£¬ÓÐÇâÆ×¡¢Ì¼Æ×ºÍDEPT Æ×£¬ÖÊÆ×
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿·ÖÀëÌá´¿µÃµ½µÄ»¯ºÏÎï¼òµ¥ÇâÆ×ºÍ̼Æ×½âÎö
ÒѾÓÐ10È˻ظ´
Çó¸ßÊÖÖ¸µã£º»¯ºÏÎïÄÜ×ö³ö1HNMR ºÍ MSµ«ÊÇ×ö²»³ö̼Æ× ÕâÊÇΪºÎ£¿
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿Çë³æÓÑÃǰï°ï½âÒ»ÏÂÕâ¸ö»¯ºÏÎï°¡£¬ÓÐÇâÆ×£¬Ì¼Æ×ºÍÖÊÆ×Êý¾Ý
ÒѾÓÐ9È˻ظ´
¡¾ÇóÖú¡¿ÇóÖú½âÆ×CÆ×ºÍHÆ×
ÒѾÓÐ22È˻ظ´
¡¾ÇóÖú¡¿±£Áôʱ¼ä²»Ò»ÑùµÄÁ½¸ö»¯ºÏÎïµÄÇâÆ×̼Æ×Ò»Ñù£¿
ÒѾÓÐ13È˻ظ´
¡¾ÇóÖú¡¿ë®´ø»¯ºÏÎï̼Æ× Çó½âÊÍ
ÒѾÓÐ10È˻ظ´

sygsy
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 24 (СѧÉú)
- ½ð±Ò: 1504.9
- É¢½ð: 5
- ºì»¨: 1
- Ìû×Ó: 112
- ÔÚÏß: 71.5Сʱ
- ³æºÅ: 3153664
- ×¢²á: 2014-04-21
- ÐÔ±ð: MM
- רҵ: Ö×Áö»¯Ñ§Ò©ÎïÖÎÁÆ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
|
1 . 2-(benzo[d]thiazole-2'-yl)-N-isoropylaniline ÏàËÆ¶È:62.5% Magnetic Resonance in Chemistry 2014 52 453-459 A comparative study between para-aminophenyl and ortho-aminophenyl benzothiazoles using NMR and DFT calculations G. K. Pierens, T. K. Venkatachalam and D. Reutens Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . 7-[(2-chlorobenzyl)oxy]-2,4-dihydro-1H-[1,2,4]triazolo[4,3-d][1,4]benzothiazin-1-one ÏàËÆ¶È:62.5% Medicinal Chemistry Research 2014 23 1829−1838 Synthesis and anticonvulsant activity evaluation of 7-alkoxy-2,4-dihydro-1H-benzo[1,2,4]triazolo[4,3-d][1,4]thiazin-1-ones in various murine experimental seizure models Xu Cao, Shi-Ben Wang, Xian-Qing Deng, Da-Chuan Liu, Zhe-Shan Quan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . alocasin B C20H18N2O5 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2012 60 670-673 Indole Alkaloids from Alocasia macrorrhiza Ling-hua Zhu, Cheng Chen, Hui Wang, Wen-cai Ye, Guang-xiong Zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . alocasin E C20H18N2O5 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2012 60 670-673 Indole Alkaloids from Alocasia macrorrhiza Ling-hua Zhu, Cheng Chen, Hui Wang, Wen-cai Ye, Guang-xiong Zhou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
3Â¥2015-06-16 11:02:38
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
wangcong123: ½ð±Ò+15, ¡ïÓаïÖú 2015-06-16 10:42:21
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wangcong123: ½ð±Ò+15, ¡ïÓаïÖú 2015-06-16 10:42:21
|
ѯ½á¹û£º¹²²éµ½4¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-(benzo[d]thiazole-2'-yl)-N-isoropylaniline ÏàËÆ¶È:62.5% Magnetic Resonance in Chemistry 2014 52 453-459 A comparative study between para-aminophenyl and ortho-aminophenyl benzothiazoles using NMR and DFT calculations G. K. Pierens, T. K. Venkatachalam and D. Reutens Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 7-[(2-chlorobenzyl)oxy]-2,4-dihydro-1H-[1,2,4]triazolo[4,3-d][1,4]benzothiazin-1-one ÏàËÆ¶È:62.5% Medicinal Chemistry Research 2014 23 1829−1838 Synthesis and anticonvulsant activity evaluation of 7-alkoxy-2,4-dihydro-1H-benzo[1,2,4]triazolo[4,3-d][1,4]thiazin-1-ones in various murine experimental seizure models Xu Cao, Shi-Ben Wang, Xian-Qing Deng, Da-Chuan Liu, Zhe-Shan Quan Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . alocasin B C20H18N2O5 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2012 60 670-673 Indole Alkaloids from Alocasia macrorrhiza Ling-hua Zhu, Cheng Chen, Hui Wang, Wen-cai Ye, Guang-xiong Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . alocasin E C20H18N2O5 ÏàËÆ¶È:60% Chemical & Pharmaceutical Bulletin 2012 60 670-673 Indole Alkaloids from Alocasia macrorrhiza Ling-hua Zhu, Cheng Chen, Hui Wang, Wen-cai Ye, Guang-xiong Zhou Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-06-16 08:25:04














»Ø¸´´ËÂ¥