| ²é¿´: 398 | »Ø¸´: 1 | |||||
·çÉñzg121ľ³æ (³õÈëÎÄ̳)
|
[ÇóÖú]
άÆÕÇóÖú ÒÑÓÐ1È˲ÎÓë
|
|
CÆ×Êý¾Ý£º21.87,112.67,121.89,122.06,127.11,127.30,130.33,131.36,133.61,134.49,135.10,135.10,135.78,145.83,163.62 ÈܼÁ£ºDMSO |
» ²ÂÄãϲ»¶
¸´ÊÔµ÷¼Á
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸±±¾©2£¬²ÄÁÏÓ뻯¹¤308Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
0817»¯Ñ§¹¤³ÌÓë¼¼ÊõÇóµ÷¼Á£¬Ò»Ö¾Ô¸Öк£Ñó319
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸µç×ӿƼ¼´óѧ085600²ÄÁÏÓ뻯¹¤ 329·ÖÇóµ÷¼Á
ÒѾÓÐ6È˻ظ´
304Çóµ÷¼Á£¨085602£¬¹ýËļ¶£¬Ò»Ö¾Ô¸985£©
ÒѾÓÐ7È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤´óѧ£¬³õÊԳɼ¨350Çóµ÷¼Á
ÒѾÓÐ14È˻ظ´
323·Ö£¨¼ÆËã»úÊÓ¾õºÍ´óÄ£ÐÍÏîÄ¿£©ÄÜÖ±½ÓÉÏÊÖ
ÒѾÓÐ3È˻ظ´
311·Ö 22408 Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´

wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½1599¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 7-hydroxytectoquinone C15H103 ÏàËÆ¶È:80% Shoyakugaku Zasshi 1990 44 95-97 A New Anthraquinone from Rubia tinctorum KAWASAKI YOKO, GODA YUKIHIRO, YOSHIHIRA KUNITOSHI, NOGUCHI HIROSHI Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . 2-hydroxy-7-methyl-9,10-anthraquinone ÏàËÆ¶È:73.3% China Journal of Chinese Materia Medica 2006 31 307-308 Studies on the chemical constituents from stem of Chirta longgangensis var. hongyao WANG Manyuan, YANG Lan, TU Youyou Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde C16H13NO3S ÏàËÆ¶È:73.3% Molecules 2014 19 1990-2003 Synthesis, Molecular and Crystal Structure Analysis of 1-(4-Methylbenzenesulfonyl)indole-3-carbaldehyde and DFT Investigation of Its Rotational Conformers Julio Zukerman-Schpector, Lucas Sousa Madureira, Glaudeston Dutra Wulf, H¨¦lio A. Stefani, Stanley N. S. Vasconcelos, Seik Weng Ng and Edward R. T. Tiekink Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 9-methyl-6H-isoindolo[2,1-a]indol-6-one C16H11NO ÏàËÆ¶È:68.7% Tetrahedron 2012 68 3112-3116 Synthesis of 6H-isoindolo[2,1-a]indol-6-ones through a sequential copper-catalyzed C-N coupling and palladium-catalyzed C¨CH activation reaction Hua-Feng He, Sheng Dong, Yi Chen, Yang Yang, Yueqin Le, Weiliang Bao Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 2,2-dibromo-1-{1-[(4-methylphenyl)sulfonyl]-1H-indol-3-yl}ethanone ÏàËÆ¶È:68.7% Helvetica Chimica Acta 2014 97 404-413 First Total Synthesis of N-(3-Guanidinopropyl)-2-(4-hydroxyphenyl)-2-oxoacetamide (pages 404¨C413) Satish S. More, Akula Raghunadh, Ramanathan Shankar, Navin B. Patel, Dinesh S. Bhalerao and Unniaran K. Syam Kumar Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-benzoylaminothiobenzamide f C14H11N3O3S ÏàËÆ¶È:66.6% Molecules 2001 6 323-337 Synthesis of Substituted 2-Benzoylaminothiobenzamides and Their Ring Closure to Substituted 2-Phenylquinazoline-4-thiones Jiř¨ª Hanusek, Ludmila Hejtm¨¢nkov¨¢, Lenka Kubicov¨¢ and Miloš Sedl¨¢k Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . 2-(p-Tolylsulfenyl)pyrrole-N-tosylpyrrole C18H17NO2S2 ÏàËÆ¶È:66.6% Canadian Journal of Chemistry 2008 86 676-681 Asymmetric oxidation of 2-(arylsulfenyl)pyrroles Alison Thompson, Jose R. Garabatos-Perera, and H. Martin Gillis Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-(4-Bromophenylcarbamoyl)-5-chlorophenyl benzenesulfonate C19H13BrClNO4S ÏàËÆ¶È:66.6% Molecules 2012 17 492-503 Antimycobacterial Activity of Salicylanilide Benzenesulfonates Martin Kr¨¢tky, Jarmila Vinšov¨¢, Nabila Guisado Rodriguez and Jiřina Stolař¨ªkov¨¢ Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Compound 6 ÏàËÆ¶È:66.6% Tetrahedron Letters 2012 53 509-513 Palladium-catalysed direct arylations of NH-free pyrrole and N-tosylpyrrole with aryl bromides Charles Beromeo Bheeter,Jitendra K. Bera,Henri Doucet Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-09-03 10:53:02














»Ø¸´´ËÂ¥