| ²é¿´: 246 | »Ø¸´: 2 | ||
smartvallyгæ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú£¬ÔÚÏߵȡ£¡£¡£Ð»Ð»£¡ ÒÑÓÐ1È˲ÎÓë
|
|
T27(D2O): 61.49,83.14,122.38,125.22,125.51,129.67,135.13,146.96,173.73 |
» ²ÂÄãϲ»¶
211±¾¿Æ²ÄÁÏ»¯¹¤Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
332Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
295Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
305Çóµ÷¼Á
ÒѾÓÐ3È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
085410 273Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
Çóµ÷¼Á£¬985²ÄÁÏÓ뻯¹¤348·Ö
ÒѾÓÐ3È˻ظ´
262Çóµ÷¼Á
ÒѾÓÐ15È˻ظ´
ɽ¶«Ê¡»ù½ð2026
ÒѾÓÐ5È˻ظ´
Ò»Ö¾Ô¸Ïôó0856£¬306Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
Çë´óÉñ¼ø¶¨´ËÖвÝҩΪºÎÎлл£¡
ÒѾÓÐ3È˻ظ´
BioTechnology : An Indian Journal µÄ¼ìË÷ÎÊÌâÌÖÂÛ
ÒѾÓÐ19È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏߵȣ¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
½âÆ×ÇóÖú£¨Ö»ÓÐ̼Æ×£©£¬Ð»Ð»ÁË¡£
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏߵȣ¬Ð»Ð»
ÒѾÓÐ4È˻ظ´
ÇóÖú¡¢¡¢¡¢Ð»Ð»´óÉñ
ÒѾÓÐ4È˻ظ´
̼Æ×ÇóÖú£¡Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬¶àлÁË
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл
ÒѾÓÐ4È˻ظ´
ºìÍâÏàËÆ¶ÈÇóÖú
ÒѾÓÐ6È˻ظ´
Journal of the American oil chemists societyͶ¸åÇóÖú
ÒѾÓÐ9È˻ظ´
΢Æ×ÇóÖú Ñϸñ°´ÕÕ¸ñʽÁгö ллÁË
ÒѾÓÐ3È˻ظ´
½ñÌìÔÙÇóÒ»´Î΢Æ× ³ê½ð20 ллÁË °´Õչ涨¸ñʽÕûÀíºÃ̼Æ×Êý¾Ý
ÒѾÓÐ3È˻ظ´
ÇóÖú¦Á-¼×»ù±½ÒÒÏ©Óë¹ýÁ¿±½·ÓÔÚÁòËá¼ÓÈÈÌõ¼þÏ·¢Éúʲô·´Ó¦£¿
ÒѾÓÐ5È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏßµÈ
ÒѾÓÐ4È˻ظ´
ÇóÖú£º¸÷λ³æÒ¯£¬Çó΢Æ×£¡°Ë°ÙÀï¼Ó¼±£¡£¡£¡¿¿ÄãÃÇÁË£¡
ÒѾÓÐ19È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
Records of Natural Products
ÒѾÓÐ7È˻ظ´

seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48433.9
- ºì»¨: 52
- Ìû×Ó: 6749
- 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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
smartvally(À±±ÊvСдú·¢): ½ð±Ò+5, Ó¦ÌûÖ÷ÇëÇó´ú·¢½ð±Ò£¬¹ÄÀøÓ¦Öú½»Á÷ 2015-03-31 10:58:16
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
smartvally(À±±ÊvСдú·¢): ½ð±Ò+5, Ó¦ÌûÖ÷ÇëÇó´ú·¢½ð±Ò£¬¹ÄÀøÓ¦Öú½»Á÷ 2015-03-31 10:58:16
|
1 . quinaldine C10H9N ÏàËÆ¶È:60% Chemistry of Natural Compounds 1996 32 932-1028 ALKALOIDS. PLANTS, STRUCTURES, PROPERTIES" Chapter , continued R. Shakirov, M. V. Telezhenetskaya, I. A. Bessonova,S. F. Aripova, I. A. Israilov, M. N. Sultankhodzhaev,V. I. Vinogradova, V. I. Akhmedzhanova, T. S. Tulyaganov,B. T. Salimov, and V. A. Tel'nov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . 2-methylquinoline ÏàËÆ¶È:60% Phytochemistry 1990 29 813-815 Molluscicidal quinoline alkaloids from Galipea bracteata Paulo C. Vieira,Isao Kubo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 4-(5-Chlorothiophen-2-yl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine C11H10NS2Cl ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2000 8 2277-2289 Glucose-6-phosphatase Catalytic Enzyme Inhibitors: Synthesis and In Vitro Evaluation of Novel 4,5,6,7-Tetrahydrothieno[3,2-c]- and -[2,3-c]pyridines Peter Madsen, Jane M. Lundbeck, Palle Jakobsen, Annemarie R. Varming, Niels Westergaard Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-(1H-1,2,4-triazol-3-ylthio)-4H-1-benzopyran-4-one C11H7N3O2S ÏàËÆ¶È:60% Heterocycles 2000 53 2191-2199 Reaction of 3-Iodochromone with Nucleophiles. 2. Reaction with Mercaptoazoles Yoshiaki Sugita,* Shengzhen Yin, and Ichiro Yokoe* Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . ethyl 3-hydroxy-3-(4-(trifluoromethyl)phenyl)propanoate ÏàËÆ¶È:60% Tetrahedron 2013 69 607-612 N-Heterocyclic carbene mediated Reformatsky reaction of aldehydes with ¦Á-trimethylsilylcarbonyl compounds Xiao-Lei Zou, Guang-Fen Du, Wan-Fu Sun, Lin He, Xiao-Wei Ma, Cheng-Zhi Gu, Bin Dai Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . 2-(4-nitrophenyl)-3-phenyl oxirane C14H11NO3 ÏàËÆ¶È:60% Tetrahedron 2013 69 6196-6202 Sequential- and tandem-oxidation¨Cepoxidation reactions employing guanidine bases David J. Phillips, Joseline L. Kean, Andrew E. Graham Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . 2-(Methyl-d3)quinoline-3-d1 ÏàËÆ¶È:60% Tetrahedron 2015 71 1425−1430 A convenient synthesis of deuterium labeled amines and nitrogen heterocycles with KOt-Bu/DMSO-d6 Yu Hu, Liang Liang, Wen-tao Wei, Xiang Sun, Xue-jing Zhang, Ming Yan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 1-(3,4-dihydro-2-thioxoquinazolin-1(2H)-yl)ethanone C10H10N2OS ÏàËÆ¶È:60% Helvetica Chimica Acta 2014 97 923-930 Synthesis of 1-Acyl-3,4-dihydroquinazoline-2(1H)-thiones by Cyclization of N-[2-(Isothiocyanatomethyl)phenyl] Amides Generated in situ from N-[2-(Azidomethyl)phenyl] Amides Kazuhiro Kobayashi and Naoki Matsumoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . 4-Amino-6-(3-nitrophenyl)-2-methylthiopyrimidine-5-carbonitrile C12H9N5O2S ÏàËÆ¶È:58.3% Journal of Heterocyclic Chemistry 2014 51 418-422 An Environmentally Benign Multicomponent Synthesis of Some Novel 2-Methylthio Pyrimidine Derivatives Using MCM-41-NH2 as Nanoreactor and Nanocatalyst Shahnaz Rostamizadeh and Masoomeh Nojavan Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . 1-((2,6-Dichloro-4-trifluoromethyl) phenyl)-4-trimethylsilanyl-1H-[1,2,3]-triazole C12H12Cl2F3N3Si ÏàËÆ¶È:55.5% Molecules 2008 13 556-566 Regioselective Synthesis of 1-(2, 6-Dichloro-4-Trifluoromethylphenyl)- 4-Alkyl-1H-[1, 2, 3]-Triazoles Huanan Hu, Anjiang Zhang, Lisheng Ding, Xinxiang Lei and Lixue Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 4-Bromomethyl-1-((2,6-dichloro-4-trifluoromethyl)phenyl)-1H-[1,2,3]-triazole C10H5BrCl2F3N3 ÏàËÆ¶È:55.5% Molecules 2008 13 556-566 Regioselective Synthesis of 1-(2, 6-Dichloro-4-Trifluoromethylphenyl)- 4-Alkyl-1H-[1, 2, 3]-Triazoles Huanan Hu, Anjiang Zhang, Lisheng Ding, Xinxiang Lei and Lixue Zhang Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 4-Chloro-quinazoline ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry 2011 19 939-950 Microwave-assisted synthesis of quinoline, isoquinoline, quinoxaline and quinazoline derivatives as CB2 receptor agonists Raimo Saari, Jonna-Carita Törmä, Tapio Nevalainen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 4-Phenyl-1,4-dihydro-5H-thieno[3,2-e][1,2,4]triazepin-5-one C12H9N3OS ÏàËÆ¶È:55.5% Zeitschrift f¨¹r Naturforschung B 2006 61b 65-68 Synthesis and Properties of Some New 1, 4-Dihydrothieno[3, 2-e][1, 2, 4]triazepin-5-ones Salim S. Sabri, Naser S. El-Abadla, Mustafa M. El-Abadelah, and Wolfgang Voelter Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-30 20:41:33
smartvally
гæ (СÓÐÃûÆø)
|
3Â¥2015-03-30 21:08:09













»Ø¸´´ËÂ¥