| ²é¿´: 300 | »Ø¸´: 1 | |||
³¾·â4004½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖú ÒÑÓÐ1È˲ÎÓë
|
| 206.5, 205.8, 172.0, 169.9, 142.5, 142.4, 129.0, 126.5, 121.2, 118.4, 75.6, 73.1, 70.0, 56.8, 36.6, 14.3, 14.2 |
» ²ÂÄãϲ»¶
269Çóµ÷¼Á
ÒѾÓÐ6È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ20È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ28È˻ظ´
267Çóµ÷¼Á
ÒѾÓÐ5È˻ظ´
¿¼Ñе÷¼Á
ÒѾÓÐ6È˻ظ´
314Çóµ÷¼Á
ÒѾÓÐ9È˻ظ´
285Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
Ò»Ö¾Ô¸¿ó´ó£¬²ÄÁϹ¤³Ìר˶314·Ö£¬0856¿Éµ÷¶¼¿ÉÒÔ
ÒѾÓÐ10È˻ظ´
»¹Óл¯¹¤¶þÂÖµ÷¼ÁµÄѧУÂð
ÒѾÓÐ31È˻ظ´
Ò»Ö¾Ô¸211 0703»¯Ñ§ 346·ÖÇóµ÷¼Á
ÒѾÓÐ15È˻ظ´
seuseasoar
ÖÁ×ðľ³æ (ÖªÃû×÷¼Ò)
- Ó¦Öú: 2238 (½²Ê¦)
- ½ð±Ò: 48419.9
- ºì»¨: 52
- Ìû×Ó: 6747
- 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
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
³¾·â4004: ½ð±Ò+10 2015-03-24 22:17:35
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
³¾·â4004: ½ð±Ò+10 2015-03-24 22:17:35
|
1 . diethyl 5-oxo-2,5-dihydrothiepino[2,3-b]indolizine-4,11-dicarboxylates C18H17NO5S ÏàËÆ¶È:55.5% Heterocycles 2009 78 319-324 First Formation of Thiepino[2,3-b]- and Thiepino[3,2-a]indolizine Derivatives Hidetoshi Isawa, Hiroyuki Suga, and Akikazu Kakehi Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 2 . ethyl 4-(4-nitrophenyl)-1-cyano-1,2,3,4-tetrahydro-1,4-epoxynaphthalene-2-carboxylate ÏàËÆ¶È:50% Heterocycles 2011 83 591-607 Synthesis and Transformations of Novel Benzo[c]furans Roberta Palk¨®, Zsuzsanna Riedl, S¨¢ndor S¨®lyom, Istv¨¢n Pallagi, Tibor Andr¨¢s Rokob, Orsolya Egyed, and György Haj¨®s Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 3 . 5-tert-butyl-3-{2-[(4S)-4-phenyl-4,5-dihydro-1,3-oxazol-2-yl]phenyl}amino-1,2,4-triazine C22H23N5O ÏàËÆ¶È:50% Tetrahedron 2013 69 7269-7278 Chiral oxazoline ligands containing a 1,2,4-triazine ring and their application in the Cu-catalyzed asymmetric Henry reaction Original Research Article Ewa Woli¨½ska Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 4 . methyl (3R,5R)-2-((S)-1-ethoxy-1-oxo-3-phenylpropan-2-yl)-3-(furan-2-yl)isoxazolidine-5-carboxylate C20H23NO6 ÏàËÆ¶È:50% Tetrahedron 2013 69 9381-9390 Stereoselective 1,3-dipolar cycloadditions of nitrones derived from amino acids. Asymmetric synthesis of N-(alkoxycarbonylmethyl)-3-hydroxypyrrolidin-2-ones Original Research Article Pedro Merino, Graziella Greco, Tom¨¢s Tejero, Ramon Hurtado-Guerrero, Rosa Matute, Ugo Chiacchio, Antonino Corsaro, Venerando Pistar¨¤, Roberto Romeo Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ 5 . (R)-3-((2R,3R,4S)-3-Nitro-2-phenylchroman-4-yl)dihydro-2H-pyran-4(3H)-one C20H19NO5 ÏàËÆ¶È:50% Tetrahedron 2012 68 5810-5816 Synthesis of substituted chiral chromans via organocatalytic kinetic resolution of racemic 3-nitro-2-aryl-2H-chromenes with ketones catalyzed by pyrrolidinyl-camphor-derived organocatalysts Dhananjay R. Magar, Kwunmin Chen Structure 13C NMR Structure & 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2015-03-24 22:14:26













»Ø¸´´ËÂ¥