| ²é¿´: 263 | »Ø¸´: 1 | ||
wdzhengqunгæ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú+15 ÒÑÓÐ1È˲ÎÓë
|
|
ÈܼÁ£ºë®´ú¼×´¼ ̼Æ×Êý¾Ý£º 24.9,25.1,31.9,34.8,49.6,67.9,90.8,143.3,153.6,205.8 ´úΪ²éÕÒ£¬Íò·Ö¸Ðл£¡ |
» ²ÂÄãϲ»¶
0703×Ü·Ö331Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
085600£¬321·ÖÇóµ÷¼Á
ÒѾÓÐ7È˻ظ´
325Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
085600£¬320·ÖÇóµ÷¼Á
ÒѾÓÐ12È˻ظ´
Ò»Ö¾Ô¸0817»¯Ñ§¹¤³ÌÓë¼¼Êõ£¬Çóµ÷¼Á
ÒѾÓÐ27È˻ظ´
Ò»Ö¾Ô¸±±¾©»¯¹¤085600 310·ÖÇóµ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸¹þ¶û±õ¹¤Òµ´óѧ085600Ó¢Ò»Êý¶þ337·ÖÇóµ÷¼Á
ÒѾÓÐ10È˻ظ´
22408Çóµ÷¼Á 354·Ö ¿É¿çרҵ
ÒѾÓÐ3È˻ظ´
277¹¤¿ÆÇóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á£¬326·Ö
ÒѾÓÐ3È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú¼¸¸ö»¯ºÏÎï΢Æ×Êý¾Ý£¬¼±¼±£¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú ³ê½ð15 Ñϸñ°´ÕÕ¸ñʽÁгöµÄ
ÒѾÓÐ4È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48394.9
- ºì»¨: 52
- Ìû×Ó: 6742
- ÔÚÏß: 546.4Сʱ
- ³æºÅ: 2400995
- ×¢²á: 2013-04-01
- ÐÔ±ð: MM
- רҵ: ʳƷ¿ÆÑ§»ù´¡
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wdzhengqun: ½ð±Ò+15, ¡ïÓаïÖú 2014-12-13 22:37:02
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
wdzhengqun: ½ð±Ò+15, ¡ïÓаïÖú 2014-12-13 22:37:02
|
1 . N-cyclohexyl-N-(5-nitro-1,3-thiazol-2-yl)urea C10H14N4O3S ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2014 22 1626-1633 2-Acylamino-5-nitro-1,3-thiazoles: Preparation and in vitro bioevaluation against four neglected protozoan parasites Carlos Nava-Zuazo, Fabiola Ch¨¢vez-Silva, Rosa Moo-Puc, Manuel Jes¨²s Chan-Bacab, Benjam¨ªn Otto Ortega-Morales, Hermenegilda Moreno-D¨ªaz, Daniel D¨ªaz-Coutiño, Emanuel Hern¨¢ndez-N¨²ñez, Gabriel Navarrete-V¨¢zquez Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 13b ÏàËÆ¶È:60% Magnetic Resonance in Chemistry 1994 32 732-738 13C NMR of 4,5-epoxy-3-substituted decalin and analogous ¦¤4-octalin derivatives: Epoxide- and methyl-induced shifts Adrian Martin Pohlit and Helena Maria Carvalho Ferraz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 4-(2-(4-Methylcyclohexyl)propane-2-yl)phenol ÏàËÆ¶È:54.5% Chemistry of Natural Compounds 2008 44 450-454 REACTION OF MENTHOL AND PHENOL IN THE PRESENCE OF ALUMINIUM ALKOXIDES I. Yu. Chukicheva, I. V. Fedorova,A. A. Koroleva, and A. V. Kuchin Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-bromo-2-{(2S)-1,4-dioxaspiro[4.5]dec-2-yl}-prop-1-ene C11H17BrO2 ÏàËÆ¶È:54.5% Russian Journal of Organic Chemistry 2010 46 1702-1708 Synthesis of epothilones molecule fragment (15R)-C13-C21 from D-mannitol V. N. Kovalenko, N. A. Sokolov and O. G. Kulinkovich Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . argyol C9H14O3 ÏàËÆ¶È:50% Planta Medica 1991 57 286-287 A New Non-Glycosidic Iridoid and a New Bisiridoid from Argylia radiata A. Bianco, P. Passacantilli, J. A. Garbarino, V. Gambaro, M. Serafini, M. Nicoletti, C. Rispoli,and G. Righi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . (1S,2S)-1-Azido-2-methylcyclohexane ÏàËÆ¶È:50% Molecules 2004 9 405-426 Synthesis of Chiral Building Blocks for Use in Drug Discovery Sharon T. Marino, Danuta Stachurska-Buczek, Daniel A. Huggins, Beata M. Krywult, Craig S. Sheehan, Thao Nguyen, Neil Choi, Jack G. Parsons, Peter G. Griffiths, Ian W. James, Andrew M. Bray, Jonathan M. White and Rustum S. Boyce Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . (2S,5R)-musclide-B(2S,5R-3) ÏàËÆ¶È:50% Natural Product Research 1997 9 297-304 Synthesis and Structure Revision of Musclides-A2 and -B Yasuhiro Tezuka; Michiko Kudoh; Yasumaru Hatanaka; Shigetoshi Kadota; Tohru Kikuchi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 5-Cyano-6-(cyclohexylamino)pyrazine-2-carboxamide C12H15N5O ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2011 19 1471-1476 Synthesis and antimycobacterial properties of N-substituted 6-amino-5-cyanopyrazine-2-carboxamides Jan Zitko, Martin Dolezal, Michaela Svobodova, Marcela Vejsova, Jiri Kunes,Radim Kucera, Petr Jilek Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . compound 13 ÏàËÆ¶È:50% Canadian Journal of Chemistry 2006 84 1388-1396 Synthesis and Lewis acid induced isomerization of mono-, di-, and tri-spiro -keto tetrahydro-furans and -pyrans1 David G. Hilmey, Peter R. Selvaraj, and Leo A. Paquette Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . choisyine ÏàËÆ¶È:50% Tetrahedron 1980 36 3579-3584 QUINOLINE ALKALOIDS-XXI THE 13C NMR SPECTRA OF HEMITERPENOID QUINOLINE ALKALOIDS AND RELATED PRENYLQUINOLINES N.M.D. BROWN,M.F. GRUNDON,D.M. HARRISON AND S.A.SURGENOR Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-N-benzylcarboxamido-3-nitroimidazo[1,2-a]pyridine C15H12N4O3 ÏàËÆ¶È:50% Journal of Heterocyclic Chemistry 2004 41 91-94 A convenient synthesis of novel pyrido(1',2':1,2)imidazo[5,4-d]-1,2,3-triazinones from imidazo[1,2-a]pyridines H¨¦ctor Salgado Zamora,Benito Rizo,Elena Campos,Rogelio Jim¨¦nez and Alicia Reyes Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . Compound 17 ÏàËÆ¶È:50% Magnetic Resonance in Chemistry 2003 41 435-440 Synthesis and 1H and 13C NMR structural analysis of cis-and trans-2-imino-1, 3-and-3, 1-perhydrobenzoxazines and their 3-and 1-N-methyl derivatives Kalevi Pihlaja, Jari Sinkkonen and Ferenc F¨¹löp Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 1b ÏàËÆ¶È:50% Tetrahedron Letters 2003 44 1409-1411 A novel one-pot synthesis of 1,2,4-triazole-3,5-diamine derivatives from isothiocyanates and mono-substituted hydrazines Chunjian Liu, Edwin J. Iwanowicz Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . compound 15 ÏàËÆ¶È:50% Bioorganic & Medicinal Chemistry 2000 8 1361-1370 Antimalarial sulfide, sulfone, and sulfonamide trioxanes Gary H. Posner, John P. Maxwell, Hardwin O'Dowd, Mikhail Krasavin, Suji Xie, Theresa A. Shapiro Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 15 . 2-trichloromethylcyclododecan-1-ol C13H23Cl3O ÏàËÆ¶È:50% Russian Journal of Organic Chemistry 2008 44 1240-1242 Additionofwaterandcarbontetrachloridetocyclododeceneinthepresenceofchromiumcatalysts T. M. Oshnyakova, N. A. Shchadneva, R. I. Khusnutdinov and U. M. Dzhemilev Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 16 . 3,3-di-methylbicyclo[2.2.1]heptane-2(S)-spiro-5'-(2'-propen-yl-1',3'-dioxolane) C14H22O2 ÏàËÆ¶È:50% Russian Journal of Organic Chemistry 2002 38 810-822 Acid-catalyzed Reactions of Camphene and ¦Á-Fenchene Epoxides O. I. Yarovaya, D. V. Korchagina, Yu. V. Gatilov and V. A. Barkhash Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 17 . 2,4,6-triisopropylacetophenone C17H26O ÏàËÆ¶È:50% Molecules 2012 17 6415-6423 Observation of 1,3-Diketones Formation in the Reaction of Bulky Acyl Chlorides with Methyllithium Jian Zhang, Nianfa Yang and Liwen Yang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 16a C36H52N4 ÏàËÆ¶È:50% Heterocycles 2012 85 749-797 The Hydrogenation of Heterocyclic Calix[4]arenes, a Transformation Leading to Novel Macrocyclic Ligands Guillaume Journot, Christopher R. Jones, Valeria Blangy, and Reinhard Neier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 19 . compound 16b C36H52N4 ÏàËÆ¶È:50% Heterocycles 2012 85 749-797 The Hydrogenation of Heterocyclic Calix[4]arenes, a Transformation Leading to Novel Macrocyclic Ligands Guillaume Journot, Christopher R. Jones, Valeria Blangy, and Reinhard Neier Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2014-12-13 17:05:00














»Ø¸´´ËÂ¥