| ²é¿´: 328 | »Ø¸´: 1 | |||
liuxiaosaľ³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú0123 ÒÑÓÐ1È˲ÎÓë
|
| 29.7, 55.3, 55.4, 55.8, 55.9, 88.2, 88.3, 100.3, 100.4, 114.2, 114.2, 116.2, 116.3, 127.8, 128.7, 128.8, 135.2, 135.2, 158.8, 160.5, 163.8, 170.9 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸±±¾©2£¬²ÄÁÏÓ뻯¹¤308Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
²ÄÁϵ÷¼Á
ÒѾÓÐ8È˻ظ´
Ò»Ö¾Ô¸Ö£ÖÝ´óѧ²ÄÁÏÓ뻯¹¤085600£¬Çóµ÷¼Á
ÒѾÓÐ24È˻ظ´
283Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
290Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
266·Ö£¬Ò»Ö¾Ô¸µçÆø¹¤³Ì£¬±¾¿Æ²ÄÁÏ£¬Çó²ÄÁÏרҵµ÷¼Á
ÒѾÓÐ12È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ8È˻ظ´
288»·¾³×¨Ë¶,Çóµ÷²ÄÁÏ·½Ïò
ÒѾÓÐ13È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ10È˻ظ´
298·Ö 070300Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×ÇóÖú£¬Ð»Ð»~
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú,лл
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú лл´ó¼Ò
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×£¬Ð»Ð»£¡
ÒѾÓÐ3È˻ظ´
΢Æ×ÇóÖú£¬ÔÚÏߵȣ¡
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
¼±Çó ÔÚÏßµÈ Î¢Æ×ÇóÖú
ÒѾÓÐ5È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖú£ºÎ¢Æ×Êý¾Ý
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎ£¡
ÒѾÓÐ5È˻ظ´
΢Æ×ÇóÖú ¼±¼±¼±£¡£¡£¡
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ7È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý£¬Ð»Ð»
ÒѾÓÐ3È˻ظ´
lifeliuyan
ÖÁ×ðľ³æ (Ö°Òµ×÷¼Ò)
- PhEPI: 1
- Ó¦Öú: 3913 (¸±½ÌÊÚ)
- ½ð±Ò: 48805.6
- É¢½ð: 890
- ºì»¨: 208
- Ìû×Ó: 4735
- ÔÚÏß: 635.4Сʱ
- ³æºÅ: 1141109
- ×¢²á: 2010-11-07
- ÐÔ±ð: MM
- רҵ: ÖÐҩҩЧÎïÖÊ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
liuxiaosa: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-01-26 10:14:40
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
liuxiaosa: ½ð±Ò+8, ¡ï¡ï¡ïºÜÓаïÖú 2015-01-26 10:14:40
|
²éѯ½á¹û£º¹²²éµ½118¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Methyl 4-(4-methoxyphenyl)-3-[2-(4-methoxyphenyl)ethynyl]isoquinolin-7-yl ether C26H21NO3 ÏàËÆ¶È:63.6% Tetrahedron 2012 68 8207-8215 Synthesis of 8-aryl substituted benzo[a]phenanthridine derivatives by consecutive three component tandem reaction and 6-endo carbocyclization Anil K. Mandadapu, Meena D. Dathi, Rajesh K. Arigela, Bijoy Kundu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . N1,N3-Bis((Z)-2-amino-1,2-dicyanovinyl)-2-(1-(tert-butylamino)-3,3-dicyano-2-(4-methoxyphenyl)propylidene)malonamide C27H25N11O3 ÏàËÆ¶È:59.0% Tetrahedron 2014 70 9512-9521 One-pot synthesis of 1,2,4,5-tetrahydro-2,4-dioxobenzo[1,4]diazepine and malonamide derivatives using multi-component reactions Abbas Rahmati, Samaneh Ahmadi, Mahdi Ahmadi-Varzaneh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . (E)-3-(3,5-Dimethoxyphenyl)-4-methoxy-2-(4-methoxyphenyl)-6-(4-methoxystyryl)benzofuran C33H30O6 ÏàËÆ¶È:58.3% European Journal of Organic Chemistry 2012 188-192 Concise Total Synthesis of Permethylated Anigopreissin A, a New Benzofuryl Resveratrol Dimer Lucia Chiummiento, Maria Funicello, Maria Teresa Lopardo, Paolo Lupattelli, Sabine Choppin and Françoise Colobert Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . 1-benzyl-3-hydroxy-3-(3-methoxybenzyl)-4-(3-methoxyphenyl)pyrrolidine-2,5-dione C26H25NO5 ÏàËÆ¶È:56.5% Molecules 2011 16 8775-8787 Divergent Synthesis of Novel Five-Membered Heterocyclic Compounds by Base-Mediated Rearrangement of Acrylamides Derived from a Novel Isocyanide-Based Multicomponent Reaction Andrea Basso, Luca Banfi and Renata Riva Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . 4-{7-Fluoro-3-[2-(4-methoxyphenyl)ethynyl]isoquinolin-4-yl}phenyl methyl ether C25H18FNO2 ÏàËÆ¶È:56.5% Tetrahedron 2012 68 8207-8215 Synthesis of 8-aryl substituted benzo[a]phenanthridine derivatives by consecutive three component tandem reaction and 6-endo carbocyclization Anil K. Mandadapu, Meena D. Dathi, Rajesh K. Arigela, Bijoy Kundu Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 6 . N1,N3-Bis((Z)-2-amino-1,2-dicyanovinyl)-2-(3,3-dicyano-1-(cyclohexylamino)-2-(4-methoxyphenyl)propylidene)malonamide C29H27N11O3 ÏàËÆ¶È:56.5% Tetrahedron 2014 70 9512-9521 One-pot synthesis of 1,2,4,5-tetrahydro-2,4-dioxobenzo[1,4]diazepine and malonamide derivatives using multi-component reactions Abbas Rahmati, Samaneh Ahmadi, Mahdi Ahmadi-Varzaneh Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 7 . compound 3 C25H24O7 ÏàËÆ¶È:54.5% Phytochemistry 1992 31 953-956 Iresinoside, a yellow pigment from Pfaffia iresinoides Yoshinori Shiobara, Shun-Suke Inoue, Yukari Nishiguchi, Keiko Kato, Tsunematsu Takemoto, Nobushige Nishimoto, Fernando de Oliveira, Gokithi Akisue, Maria Kubota Akisue, Goro Hashimoto Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 8 . 2',4'-Dimethoxy-5,6-benzoflavone ÏàËÆ¶È:54.5% Magnetic Resonance in Chemistry 2012 50 62-67 Synthesis of methoxybenzoflavones and assignments of their NMR data Doseok Hwang, Geunhyeong Jo, Jiye Hyun, Sung Dae Lee, Dongsoo Kohc and Yoongho Lim Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 9 . Compound 17 ÏàËÆ¶È:54.5% Magnetic Resonance in Chemistry 2006 44 895-900 1H, 13C and 15N NMR spectral characterization of twenty-seven 1, 2-diaryl-(4E)-arylidene-2-imidazolin-5-ones (pages 895¨C900) Katri Laihia, Erkki Kolehmainen, Vladimir Nikiforov and Sergei Miltsov Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 10 . gnetin C C28H20O6 ÏàËÆ¶È:54.5% Heterocycles 2001 55 2123-2130 Four New Glucosides of Stilbene Oligomers from the Stem of Gnetum gnemonoides Ibrahim Iliya, Toshiyuki Tanaka,* Miyuki Furasawa, Zulfiqar Ali, Ken-ichi Nakaya, Munekazu Iinuma, Yoshiaki Shirataki, Jin Murata, and Dedy Darnaedi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 11 . 7-amino-3-(3-fluorobenzyl)-1-methyl-2,4-dioxo-5-phenyl-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine-6-carbonitrile C22H16FN5O2 ÏàËÆ¶È:54.5% Molecules 2012 17 2351-2366 Syntheses and Cell-Based Phenotypic Screen of Novel 7-Amino pyrido[2,3-d]pyrimidine-6-carbonitrile Derivatives as Potential Antiproliferative Agents Tao Yang, Hong He, Wei Ang, Ying-Hong Yang, Jian-Zhong Yang, Yan-Ni Lin, Hua-Cheng Yang, Wei-Yi Pi, Zi-Cheng Li, Ying-Lan Zhao, You-Fu Luo and Yuquan Wei Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 12 . 2-bromo-8,10-dimethoxy-11-(2,4,6-trimethoxyphenyl)-6,11-dihydrodibenzo[b,e]oxepine C23H27BrO6 ÏàËÆ¶È:54.5% European Journal of Organic Chemistry 2011 2133-2141 A Facile One-Pot Access to Dibenzo[b,e]oxepines by a Lewis Acid Catalysed Tandem Reaction Chada R. Reddy, Palacherla Ramesh, Nagavaram N. Rao and Saiyed A. Ali Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 13 . 2-(4-fluorophenyl)-3-(4-methoxyphenyl)-3,4-dihydro-2H-1,3-benzoxazine C21H18FNO2 ÏàËÆ¶È:54.5% Molecules 2012 17 8174-8185 Synthesis and Fungicidal Activity of Novel 2,3-Disubstituted-1,3-benzoxazines Zilong Tang, Zhonghua Zhu, Zanwen Xia, Hanwen Liu, Jinwen Chen, Wenjing Xiao and Xiaoming Ou Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 14 . 3-allyl-4,4-divinyl-2,3,3a,4,5,5a-hexahydro-1H-pyrrolo[3',2':2,3]cyclopenta[1,2-c]quinolin-6(7H)-one C21H24N2O ÏàËÆ¶È:54.5% Tetrahedron 2013 69 1434-1445 Synthesis studies on the Melodinus alkaloid meloscine Ken S. Feldman, Joshua F. Antoline Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2015-01-23 19:38:20














»Ø¸´´ËÂ¥