| ²é¿´: 267 | »Ø¸´: 1 | |||
guohuanjieľ³æ (ÕýʽдÊÖ)
|
[ÇóÖú]
ÇóÖú΢Æ×Êý¾Ý²éѯ
|
|
13C NMR(ë®´úßÁà¤)£º44.0,51.1,56.5,114.5,117.4,117.6,117.6,126.5,128.1,129.6,129.6,132.5,132.4, 135.5,149.4,150.2,158.8,173.8 |
» ²ÂÄãϲ»¶
263Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
293µ÷¼Á
ÒѾÓÐ3È˻ظ´
»úе¹¤³Ì264ѧ˶Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
264Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
22408 266Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
273Çóµ÷¼Á
ÒѾÓÐ43È˻ظ´
307Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
327Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
10½ð±ÒÇóÖú΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
mzp-0
ľ³æ (ÕýʽдÊÖ)
- Ó¦Öú: 138 (¸ßÖÐÉú)
- ½ð±Ò: 3037.8
- ºì»¨: 3
- Ìû×Ó: 425
- ÔÚÏß: 45.1Сʱ
- ³æºÅ: 1739290
- ×¢²á: 2012-04-06
- ÐÔ±ð: MM
- רҵ: ÖÐÒ©ÖÊÁ¿ÆÀ¼Û
¡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
guohuanjie: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-12 19:43:55
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
guohuanjie: ½ð±Ò+20, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-06-12 19:43:55
|
1 . 4-benzyl-2-methoxy-4H-[1,2,4]triazolo[1,5-a]quinazolin-5-one C17H14N4O2 ÏàËÆ¶È:66.6% Journal of Heterocyclic Chemistry 2011 48 656-662 Synthesis of novel 2-alkoxy(aralkoxy)-4H-[1,2,4]triazolo[1,5-a]quinazolin-5-ones starting with dialkyl-N-cyanoimidocarbonates Rashad Al-Salahi and Detlef Geffken Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . Tetrahydro-¦Ã-carboline ÏàËÆ¶È:63.1% Tetrahedron Letters 2005 46 7881-7884 Preparation of RCM substrates for azepinoindole synthesis: reductive amination versus tetrahydro-¦Ã-carboline formation M.-Lluïsa Bennasar, Ester Zulaica, Sandra Alonso Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . 3-(6-phenyl-2,3'-bipyridin-4-yl)phenol ÏàËÆ¶È:63.1% Bioorganic & Medicinal Chemistry 2010 18 3066-3077 Synthesis, topoisomerase I and II inhibitory activity, cytotoxicity, and structure¨Cactivity relationship study of hydroxylated 2, 4-diphenyl-6-aryl pyridines Radha Karki, Pritam Thapa, Mi Jeong Kang, Tae Cheon Jeong, Jung Min Nam, Hye-Lin Kim, Younghwa Na, Won-Jea Cho, Youngjoo Kwon, Eung-Seok Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . podonaka A C18H16O4 ÏàËÆ¶È:61.1% Journal of Asian Natural Products Research 2009 11 410-416 A new dimeric phenylpropanoid and cytotoxic norditerpene constituents from Podocarpus nakaii Syh-Yuan Huang, Long-Yun Fanb, Ya-Ching Shend, Chia-Ching Liao, Li-Chuan Hsu,Ya-Wen Hsu, Tian-Shan Wu, Ping-Chun Hsiao, Chien-Chang Shen, Ming-Jaw Don and Yao-Haur Kuo Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 3-(2-hydroxyphenyl)-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazine C18H15NO2 ÏàËÆ¶È:61.1% Journal of Heterocyclic Chemistry 2004 41 367-373 Transformation reactions of the betti base analog aminonaphthols Istv¨¢n Szatm¨¢ri,Anaszt¨¢zia Het¨¦nyi,L¨¢szl¨® L¨¢z¨¢r and Ferenc F¨¹löp Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . 2,6-bis(6'-cyano-4'-phenyl-2'-quinolinyl)benzene ÏàËÆ¶È:61.1% Journal of Heterocyclic Chemistry 2000 37 1225-1231 Synthesis and characterization of new substituted terdentate 2,6-bis(2'-quinolinyl)pyridine and 1,3-bis(2'-quinolinyl)-benzene ligands for transition metals Antonino Mamo Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . (7-amino-5-phenylimidazo[1,5-b]pyridazin-3-yl)(2-hydroxy-5-methoxyphenyl)methanone C20H16N4O3 ÏàËÆ¶È:61.1% Heterocycles 2008 75 1765-1772 A Facile Synthesis of Imidazo[1, 5-b]pyridazines from 3-Formylchromones Andrey S. Plaskon, Sergey V. Ryabukhin, Dmitriy M. Volochnyuk, Alexander N. Shivanyuk, and Andrey A. Tolmachev Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 4-(4-chlorobenzoyl)-2-phenyl-9a,9b,3a,4-tetrahydropyrrolo[3',4':3,4]pyrrolo[1,2-b]pyridazine-1,3-dione C22H16N3O3Cl ÏàËÆ¶È:61.1% Heterocycles 2005 65 1871-1879 Synthesis and Antimicrobial Activity of Some New Pyridazine Derivatives Maria D. Caprosu, Roxana M. Butnariu, and Ionel I. Mangalagiu* Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2-bromo-N-(2-hydroxybenzyl)-N-(4-methoxyphenyl)-3-phenylpropionamide C23H22NO3Br ÏàËÆ¶È:61.1% Heterocycles 2004 63 1093-1112 Synthesis of Substituted 1,4-Benzoxazepin-3-one Derivatives Yann Davion, G¨¦rald Guillaumet, Jean-Michel L¨¦ger, Christian Jarry, Brigitte Lesur, and Jean-Yves M¨¦rour* Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Compound 20 ÏàËÆ¶È:61.1% Magnetic Resonance in Chemistry 2008 46 299-305 1H and 13C NMR data of benzylsulfonic acids¡ªmodel compounds for lignosulfonate (pages 299¨C305) Bjart F. Lutnaes, Bernt O. Myrvold, Rolf A. Lauten and Molla M. Endeshaw Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . (2S,E)-N-[ 2-hydroxy-2-(4-hydroxyphenyl)ethyl] ferulamide ÏàËÆ¶È:61.1% Chinese Traditional and Herbal Drugs 2009 40 689-693 Water-soluble constituents of Clerodendranthus spicatus CHEN Yi-lei; TAN Jun-jie; LU Lu-lu; TAN Chang-heng; JIANG Shan-hao; ZHU Da-yuan Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . 3-(4-Chlorophenyl)-5-(pyridin-4-yl)-4-(2-fluoro-4-chlorobenzylidenamino)-4H-1,2,4-triazole C20H12N5Cl2F ÏàËÆ¶È:61.1% Zeitschrift f¨¹r Naturforschung B 2008 63 548-554 Synthesis and Antioxidant Properties of Some New 3-(4-Chlorophenyl)-5-(pyridin-4-yl)-4H-1,2,4-triazole Derivatives O. Bekircan, T. Özen, N. G¨¹mr¨¹kc¨¹o\uglu, and H. Bekta\cs Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . compound 4b C22H25NOS ÏàËÆ¶È:61.1% Heterocycles 2002 57 1989-1995 A New Simple Method for the Synthesis of Thiophene Derivatives ¡ª Generation of Thiocarbonyl Ylides form S-¦Á-(Dimethylphenylsilyl)benzyl Acylates and Their Cycloaddition with Acetylenic Dipolarophiles ¡ª Mitsuo Komatsu,* Jinil Choi, Masatoshi Mihara, Yoji Oderaotoshi, and Satoshi Minakata Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . (E)-ethyl 3-(1'-(4''-methoxyphenyl)-3'-phenyl-1'H-pyrazol-4'-yl) acrylate C21H20N2O3 ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2010 18 4338-4350 Novel pyrazole derivatives: Synthesis and evaluation of anti-angiogenic activity Michael S. Christodoulou, Sandra Liekens, Konstantinos M. Kasiotis, Serkos A. Haroutounian Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . (E)-3-(1'-(4''-methoxyphenyl)-3'-phenyl-1'H-pyrazol-4'-yl) acrylic acid C19H16N2O3 ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2010 18 4338-4350 Novel pyrazole derivatives: Synthesis and evaluation of anti-angiogenic activity Michael S. Christodoulou, Sandra Liekens, Konstantinos M. Kasiotis, Serkos A. Haroutounian Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . methyl 5-methoxy-2-[N-(2-oxopent-4-enyl)trifluoroacetamido]benzoate C16H16NO5F3 ÏàËÆ¶È:61.1% The Journal of Organic Chemistry 2010 75 8508-8515 Isolation, Structural Assignment, and Total Synthesis of Barmumycin Adriana Lorente, Daniel Pla, Librada M. Canedo, Fernando Albericio, and Mercedes Alvarez Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 5-nitro-7-((4-tosylpiperazin-1-yl)methyl)quinolin-8-ol C21H22N4O5S ÏàËÆ¶È:61.1% Bioorganic & Medicinal Chemistry 2009 17 7239-7247 Synthesis and pharmacological exploitation of clioquinol-derived copper-binding apoptosis inducers triggering reactive oxygen species generation and MAPK pathway activation Hui-Ling Chen, Chun-Yi Chang, Hsun-Tzu Lee, Hua-Hsuan Lin, Pei-Jung Lu, Chia-Ning Yang, Chung-Wai Shiau, Arthur Y. Shaw Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . 4-(2,4-dichlorobenzyl)-2-ethoxy-4H-[1,2,4]triazolo[1,5-a]quinazolin-5-one C18H14Cl2N4O2 ÏàËÆ¶È:61.1% Journal of Heterocyclic Chemistry 2011 48 656-662 Synthesis of novel 2-alkoxy(aralkoxy)-4H-[1,2,4]triazolo[1,5-a]quinazolin-5-ones starting with dialkyl-N-cyanoimidocarbonates Rashad Al-Salahi and Detlef Geffken Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-06-12 15:06:29














»Ø¸´´ËÂ¥