| ²é¿´: 226 | »Ø¸´: 4 | ||
Ö£µÂµÂͳæ (³õÈëÎÄ̳)
|
[ÇóÖú]
άÆ×ÇóÖú
|
| 190.513,189.639,137.824,136.211,136.145,135.416,134.912,129.736,124.027,110.217,67.56,66.108,43.156,41.253,40.440,32.452,31.481,30.644,26.85,14.114 |
» ²ÂÄãϲ»¶
368»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
0703»¯Ñ§Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
µ÷¼Á
ÒѾÓÐ3È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ13È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ18È˻ظ´
»úе¹¤³Ì313·ÖÕÒ¹¤¿Æµ÷¼Á
ÒѾÓÐ3È˻ظ´
¿¼Ñе÷¼Á-²ÄÁÏÀà-284
ÒѾÓÐ9È˻ظ´
Ò»Ö¾Ô¸ÏôóÉúÎïѧ332Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
±¾¿Æ211£¬293·ÖÇëÇóµ÷¼Á
ÒѾÓÐ13È˻ظ´
sunwen1111
Òø³æ (ÕýʽдÊÖ)
- Ó¦Öú: 29 (СѧÉú)
- ½ð±Ò: 961.2
- É¢½ð: 219
- ºì»¨: 2
- Ìû×Ó: 455
- ÔÚÏß: 158.7Сʱ
- ³æºÅ: 1406398
- ×¢²á: 2011-09-18
- ÐÔ±ð: MM
- 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 ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
karl2100: ½ð±Ò+1, лл£¡ 2013-01-07 00:28:06
Ö£µÂµÂ: ½ð±Ò+25, ¡ï¡ï¡ïºÜÓаïÖú, ͦºÃµÄ 2013-01-07 08:52:23
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
karl2100: ½ð±Ò+1, лл£¡ 2013-01-07 00:28:06
Ö£µÂµÂ: ½ð±Ò+25, ¡ï¡ï¡ïºÜÓаïÖú, ͦºÃµÄ 2013-01-07 08:52:23
|
²éѯ½á¹û£º¹²²éµ½11¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) -------------------------------------------------------------------------------- 1 . N,N'-Bis(octyl)-1,7-bis(2,3,4,5,6-pentafluorophenyl)perylene-3,4 : 9,10-bis(dicarboximide) C52H37F10N2O4 ÏàËÆ¶È:50% Helvetica Chimica Acta 2009 92 2525-2531 Synthesis and Characterization of Pentafluorophenyl-Substituted Perylenebis(dicarboximides) Tobias Schnitzler, Chen Li, Klaus M¨¹llen Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . paralemnolin K C17H26O3 ÏàËÆ¶È:50% Chemical & Pharmaceutical Bulletin 2010 58 30-33 Paralemnolins J¡ªP, New Sesquiterpenoids from the Soft Coral Paralemnalia thyrsoide Guey-Horng Wang, Ho-Cheng Huang, Jui-Hsin Su, Yang-Chang Wu and Jyh-Horng Sheu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . compound 2 ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 551-554 Stereoselective synthesis towards the C8¨CC18 subunit of pamamycin-607 induced by a chiral sulfoxide group Guy Solladi¨¦, Xavier J. Salom-Roig, Gilles Hanquet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . (2E,6S,8S)-3a ÏàËÆ¶È:50% Tetrahedron Letters 2000 41 2737-2740 Diastereodivergent synthesis of the C8¨CC18 precursor and C1¡ä¨CC11¡ä subunit of pamamycin 607 induced by a chiral sulfoxide group Guy Solladi¨¦, Xavier J. Salom-Roig, Gilles Hanquet Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . methyl (6R,1'R)-5-ethyloxycarbonyl-6-[2'-amino-1'-(1''H-imidazol-4''-yl)-ethyl]-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridin-6-carboxylate ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2003 40 917-923 Synthesis of new 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine derivatives Miguel F. Braña Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . compound 7 ÏàËÆ¶È:50% Tetrahedron Letters 2002 43 3939-3941 Chiral cyclopropanes: asymmetric synthesis of constanolactones A and B Jurong Yu, Jing-Yu Lai, Jianhua Ye, Narayanan Balu, L.Manmohan Reddy, Wenhu Duan, Elaine R. Fogel, Jorge H. Capdevila, J.R. Falck Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . 4-Ethoxymethyl-2,6-dimethyl-3-o-tolyl-2H-isoquinolin-1-one ÏàËÆ¶È:50% Tetrahedron 2012 68 250-261 Synthesis of 12-oxobenzo[c]phenanthridinones and 4-substituted 3-arylisoquinolones via Vilsmeier¨CHaack reaction Daulat Bikram Khadka, Su Hui Yang, Suk Hee Cho, Chao Zhao, Won-Jea Cho Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . N-2-(triphenylsilyl)ethoxycarbonyl-N'-benzyloxycarbonyl-1,6-diaminohexane C35H40N2O4Si ÏàËÆ¶È:50% molecules 2011 16 4695-4718 The 2-(Triphenylsilyl)ethoxycarbonyl-(¡°Tpseoc¡±-) Group: A New Silicon-Based, Fluoride Cleavable Oxycarbonyl Protecting Group Highly Orthogonal to the Boc-, Fmoc-and Cbz-Groups Martin Golkowski and Thomas Ziegler Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . compound 2w C22H25FN2O ÏàËÆ¶È:50% Journal of Medicinal Chemistry 1993 36 2908-2920 Chemistry, binding affinities, and behavioral properties of a new class of "antineophobic" mitochondrial DBI receptor complex (mDRC) ligands A. P. Kozikowski, D. Ma, James Brewer, S. Sun, E. Costa, E. Romeo, A. Guidotti Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . monacolin L ÏàËÆ¶È:50% Acta Pharmaceutica Sinica 2011 46 564-567 A new monacolin analogue from Xuezhikang capsule LI Xue-mei, SHEN Xing-hai, DUAN Zhen-wen, GUO Shu-ren* Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . 2-(2,3-Dimethylphenyl)-1-morpholino-2-(piperidin-1-yl)ethanone C19H28N2O2 ÏàËÆ¶È:50% Tetrahedron 2012 68 4710-4718 A formal method for the de-N,N-dialkylation of Sommelet¨CHauser rearrangement products Eiji Tayama, Ryota Sato, Keisuke Takedachi, Hajime Iwamoto, Eietsu Hasegawa Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-01-06 17:09:37
Ö£µÂµÂ
ͳæ (³õÈëÎÄ̳)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 20.4
- É¢½ð: 6
- Ìû×Ó: 30
- ÔÚÏß: 11.7Сʱ
- ³æºÅ: 2031628
- ×¢²á: 2012-09-26
- רҵ: ÌìȻҩÎﻯѧ
3Â¥2013-01-06 21:02:40
sunwen1111
Òø³æ (ÕýʽдÊÖ)
- Ó¦Öú: 29 (СѧÉú)
- ½ð±Ò: 961.2
- É¢½ð: 219
- ºì»¨: 2
- Ìû×Ó: 455
- ÔÚÏß: 158.7Сʱ
- ³æºÅ: 1406398
- ×¢²á: 2011-09-18
- ÐÔ±ð: MM
- רҵ: ÌìÈ»Óлú»¯Ñ§
4Â¥2013-01-06 22:37:19
Ö£µÂµÂ
ͳæ (³õÈëÎÄ̳)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 20.4
- É¢½ð: 6
- Ìû×Ó: 30
- ÔÚÏß: 11.7Сʱ
- ³æºÅ: 2031628
- ×¢²á: 2012-09-26
- רҵ: ÌìȻҩÎﻯѧ
5Â¥2013-01-07 08:53:27














»Ø¸´´ËÂ¥