| ²é¿´: 254 | »Ø¸´: 1 | ||
[ÇóÖú]
΢Æ×ÇóÖú²é»¯ºÏÎï
|
| 13C NMR (100 MHz, Methanol) ¦Ä8.5, 12.2, 12.6, 20.6, 31.2, 36.1, 111.4, 116.7, 125.3, 134.0, 143.3, 147.1, 148.6, 162.6, 186.9 |
» ²ÂÄãϲ»¶
Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
085600²ÄÁÏÓ뻯¹¤×¨Ë¶329 Çóµ÷¼Á
ÒѾÓÐ18È˻ظ´
274Çóµ÷¼ÁÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
277¡¢Ñ§Ë¶£¬Çóµ÷¼Á ÊýÒ»104£¬
ÒѾÓÐ8È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤085600£¬Çóµ÷¼Á
ÒѾÓÐ32È˻ظ´
085602»¯Ñ§¹¤³Ì268·Ö¶×µ÷¼Á
ÒѾÓÐ13È˻ظ´
»·¾³×¨Ë¶µ÷¼Á
ÒѾÓÐ12È˻ظ´
»¯Ñ§¹¤³Ìµ÷¼Á289
ÒѾÓÐ17È˻ظ´
²ÄÁÏÓ뻯¹¤×¨Ë¶306·ÖÕÒºÏÊʵ÷¼Á
ÒѾÓÐ15È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú] ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú²é»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ Èý¸ö»¯ºÏÎï
ÒѾÓÐ3È˻ظ´
MestReNovaÎÞ·¨½øÐл¯ºÏÎï½á¹¹ÇâÆ×Ô¤²â
ÒѾÓÐ12È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯ3¸ö»¯ºÏÎïµÄÄ£ºý²éÕÒ£¨¡·80%£©
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý¿â²éѯһ¸ö»¯ºÏÎï~¼±~£¡Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÍÆ¼ö¹ØÓÚ»¯ºÏÎï½á¹¹Óë»îÐÔ¹ØÏµµÄÆÚ¿¯
ÒѾÓÐ4È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
¡¾ÇóÖú¡¿ËÖªµÀÄÄÀï¿ÉÒԲ黯ºÏÎïµÄ̼Æ×°¡£¿
ÒѾÓÐ10È˻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 ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
izzi: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-09 10:55:13
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
izzi: ½ð±Ò+20, ¡ï¡ï¡ïºÜÓаïÖú 2013-09-09 10:55:13
|
²éѯ½á¹û£º¹²²éµ½11¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Compound IIg ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 2003 41 291-295 Synthesis and complete NMR characterization of 4-alkyl-2-(6-substituted-1, 3-benzoxazol-2-yl)benzenols V. Sridharan, S. Muthusubramanian and S. Sivasubramanian Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 7-tert-butyl-4,5-dichloro-2-(4-methylphenyl)-1,3-benzoxazol-6-ol C18H17Cl2NO2 ÏàËÆ¶È:53.3% Russian Journal of Organic Chemistry 2011 47 1508-1514 Halogenation of N-substituted p-quinone monoimines and p-quinone monooxime ethers: XIII. Specificity of bromination of N-Acetyl(aroyl)-1,4-benzoquinone monoimines A. P. Avdeenko, S. A. Konovalova, O. P. Ledeneva, O. N. Ludchenko and G. V. Palamarchuk, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-methyl-1-phenyl-5-p-tolyl-1H-pyrazolo[3,4-b]pyridine C20H17N3 ÏàËÆ¶È:53.3% Tetrahedron 2013 69 1217-1228 Design, synthesis and transformation of some heteroannulated 3-aminopyridines¡ªpurine isosteres with exocyclic nitrogen atom Viktor O. Iaroshenko, Marcelo Vilches-Herrera, Ashot Gevorgyan, Satenik Mkrtchyan, Knar Arakelyan, Dmytro Ostrovskyi, Muhammad S.A. Abbasi, Linda Supe, Ani Hakobyan, Alexander Villinger, Dmitriy M. Volochnyuk, Andrei Tolmachev Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . phomalevone B C30H26O10 ÏàËÆ¶È:53.3% Journal of Natural Products 2011 74 395-401 Phomalevones A−C: Dimeric and Pseudodimeric Polyketides from a Fungicolous Hawaiian Isolate of Phoma sp. (Cucurbitariaceae) Sang Hee Shim, Jonas Baltrusaitis, James B. Gloer, and Donald T. Wicklow Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2,2'-(4,4'-(3,4-Dimethylthieno[2,3-b]thiophene-2,5-diyl)bis(thiazole-4,2-Diyl)) bis (3-(4-chlorophenyl)acrylonitrile C32H18N4S4Cl2 ÏàËÆ¶È:53.3% International Journal of Molecular Sciences 2012 13 5035-5047 A Novel and Expedient Approach to New Thiazoles, Thiazolo[3,2-a]pyridines, Dihydrothiophenes, and Hydrazones Incorporating Thieno[2,3-b]thiophene Moiety Yahia Nasser Mabkhot, Assem Barakat, Abdullah Mohammad Al-Majid, Abdullah Saleh Alamary and Taleb T. Al-Nahary Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (3¦Â,6¦Â,10¦Â)-3-acetyl-6,10-dihydroxyeremophila-7(11),8-dieno-12,8- lactone ÏàËÆ¶È:52.9% Helvetica Chimica Acta 2009 92 495-501 New Eremophilane Sesquiterpenes from the Roots of Ligularia fischeri Meicai Deng, Weiwei Dong, Wei Jiao, Runhua Lu Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . Compound IId ÏàËÆ¶È:52.9% Magnetic Resonance in Chemistry 2003 41 291-295 Synthesis and complete NMR characterization of 4-alkyl-2-(6-substituted-1, 3-benzoxazol-2-yl)benzenols V. Sridharan, S. Muthusubramanian and S. Sivasubramanian Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 3¦Â-angeloyloxy-6¦Â,10¦Â-dihydroxyeremophila-7(11),8(9)-dien-8,12-olide C20H26O6 ÏàËÆ¶È:50% Planta Medica 2003 69 745-749 New Eremophilane Sesquiterpenes from Cacalia ainsliaeflora Manjun Mao,Zhongduo Yang,Zhongjian Jia Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 1-(2,5-dihydroxy-3,4-dimethylphenyl)-2-(3',4'-dihydroxyphenyl)-ethanone C16H16O5 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2009 57 346-360 Synthesis of Various Kinds of Isoflavones, Isoflavanes, and Biphenyl-Ketones and Their 1,1-Diphenyl-2-picrylhydrazyl Radical-Scavenging Activities Hideyuki Goto, Yoshiyasu Terao and Shuji Akai Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . 2-hydroxy-6-(12-phenyldodecyl)-benzoic acid ÏàËÆ¶È:50% Phytochemistry 1990 29 1995-1998 Cyclic farnesyl-coumarin and farnesyl-chromone derivatives from Ferula communis subsp. Communis Mahmut Miski,Jasmin Jakupovic Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 3-butyl-2-(4-nitrophenyl)-2,3-dihydroquinazolin-4(1H)-one C18H19N3O3 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2011 48 1419-1427 One-pot synthesis of 2,3-disubstituted-2,3-dihydroquinazolin-4(1H)-ones using [Hmim][NO3]: An eco-friendly protocol Iraj Mohammadpoor-Baltork, Ahmad Reza Khosropour, Majid Moghadam, Shahram Tangestaninejad, Valiollah Mirkhani, Mohammad Soltani and Arsalan Mirjafari Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-09-04 16:30:05














»Ø¸´´ËÂ¥