| ²é¿´: 254 | »Ø¸´: 1 | ||||
zhaocaiguiÒø³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×ÇóÖúÒ»»¯ºÏÎï½á¹¹
|
|
13C NMR (101 MHz, CDCl3) ¦Ä 52.82,112.88,117.50,131.14,132.35,132.51,132.73,134.79,164.46 |
» ²ÂÄãϲ»¶
Ò»Ö¾Ô¸»ªÄÏʦ·¶´óѧ0702ÎïÀíѧ305µ÷¼Á
ÒѾÓÐ5È˻ظ´
Çóµ÷¼Á
ÒѾÓÐ30È˻ظ´
266Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
297Çóµ÷¼Á
ÒѾÓÐ16È˻ظ´
326·Ö£¬Ò»Ö¾Ô¸»¦9£¬ÇóÉúÎïѧµ÷¼Á
ÒѾÓÐ4È˻ظ´
288Çóµ÷¼Á£¬Ò»Ö¾Ô¸»ªÄÏÀí¹¤´óѧ071005
ÒѾÓÐ3È˻ظ´
304Çóµ÷¼Á
ÒѾÓÐ13È˻ظ´
µ÷¼Á
ÒѾÓÐ18È˻ظ´
293µ÷¼Á
ÒѾÓÐ4È˻ظ´
338Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×Ç󻯺ÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇëÎÊÈçºÎ¸ù¾ÝÇâÆ×̼Æ×Êý¾ÝÍÆ²â»¯ºÏÎï½á¹¹
ÒѾÓÐ6È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
΢Æ×ÇóÖú»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
MestReNovaÎÞ·¨½øÐл¯ºÏÎï½á¹¹ÇâÆ×Ô¤²â
ÒѾÓÐ12È˻ظ´
΢Æ×ÇóÖúÒ»»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
Çó΢Æ×¼ìË÷»¯ºÏÎï½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÍÆ¼ö¹ØÓÚ»¯ºÏÎï½á¹¹Óë»îÐÔ¹ØÏµµÄÆÚ¿¯
ÒѾÓÐ4È˻ظ´
ÇóÖúÓÃCDÆ×½âÎöÒ»¸öÄ¾Ö¬ËØÀ໯ºÏÎïµÄ¾ø¶Ô¹¹ÐÍ
ÒѾÓÐ7È˻ظ´
ÇóÖúÒ»»¯ºÏÎï΢Æ×Êý¾Ý½á¹¹
ÒѾÓÐ3È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
ÇëÎÊÓÐûÓÐÒ»¸ö»¯ºÏÎï±ê×¼Æ×ͼ½âÎöÊý¾Ý¿â£¿
ÒѾÓÐ5È˻ظ´
¡¾ÇóÖú¡¿¼û¹íµÄÁ½¸ö»¯ºÏÎï½á¹¹½âÎö
ÒѾÓÐ18È˻ظ´
wangkaibo123
ÈÙÓþ°æÖ÷ (Ö°Òµ×÷¼Ò)
kerry
-

ר¼Ò¾Ñé: +726 - PhEPI: 3
- Ó¦Öú: 1928 (½²Ê¦)
- ¹ó±ö: 0.598
- ½ð±Ò: 7869.1
- É¢½ð: 10156
- ºì»¨: 100
- Ìû×Ó: 3780
- ÔÚÏß: 1007.1Сʱ
- ³æºÅ: 2088618
- ×¢²á: 2012-10-26
- ÐÔ±ð: GG
- רҵ: ¿¹Ö×ÁöÒ©ÎïÒ©Àí
- ¹ÜϽ: ҩѧ
¡¾´ð°¸¡¿Ó¦Öú»ØÌû
¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï ¡ï
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhaocaigui(¶¹¸ç´ú·¢): ½ð±Ò+8, лл 2013-09-21 11:23:23
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
zhaocaigui(¶¹¸ç´ú·¢): ½ð±Ò+8, лл 2013-09-21 11:23:23
|
²éѯģʽ£ºÄ£ºý²éѯ ̼Æ×Êý¾ÝÊäÈ룺 °´´ÓСµ½´ó˳ÐòÊäÈ룬Êý×Ö¼äÓÃÓ¢Îİë½Ç¶ººÅ(,)·Ö¸ôÀýÈ磺 21.4,30.4,37.4,73.2,73.7,125.6,126.6,139.6,140.2,168.2 ÈܼÁÑ¡Ï Æ¥ÅäÈݲ (Êý×Ö¸ñʽ£¬¿É×ÔÐÐÉ趨) ÏàËÆ¶È£º %(ÏàËÆ¶È>=50%) ²éѯ½á¹û£º¹²²éµ½186¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . Methyl 2,5-dichlorobenzoate ÏàËÆ¶È:77.7% Zeitschrift f¨¹r Naturforschung B 2008 63 1291-1299 Electroreduction of Organic Compounds, 36. Electroreduction of Chlorinated Methyl Benzoates J. Gassmann and J. Voss Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . furan-2-yl(2-methoxy-2-oxoethyl)diphenylphosphonium bromide C19H18BrO3P ÏàËÆ¶È:72.7% Tetrahedron 2013 69 7395-7402 Annelated P-containing heterocycles from aryl- and hetaryl-substituted phosphonium iodonium ylides with a methoxycarbonyl-group Original Research Article Elena D. Matveeva, Tatyana A. Podrugina, Marina A. Taranova, Ekaterina Yu. Melikhova, Rolf Gleiter, Nikolay S. Zefirov Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . iminophosphorane ÏàËÆ¶È:66.6% The Journal of Organic Chemistry 2002 67 7797-7801 Thermolysis of Benzannulated Enyne−Carbodiimides. Application in the Synthesis of Pyrido[1¡®,2¡®:1,2]pyrimido[4,5-b]indoles and Related Heteroaromatic Compounds Xiaoling Lu, Jeffrey L. Petersen, and Kung K. Wang Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . methyl (E)-3-phenyl-3-trifluoromethylsulfonyloxy-2-propenoate ÏàËÆ¶È:66.6% Russian Journal of Organic Chemistry 2005 41 1485-1492 Protonation of 3-Arylpropynoic Acid Derivatives in Superacids S. Walspurger, A. V. Vasil'ev, J. Sommer, P. Pale and P. Yu. Savechenkov, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . ¦Á,¦Á'-bis(4-trifluoromethylbenzylammonium)-p-xylene bis(hexafluorophosphate) C24H24F18N2P2 ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2011 759-769 Synthesis and Complexation Studies between Trifluoromethylammonium Threads and Dibenzo[24]Crown-8 Carsten Johnsen, Paul C. Stein, Kent A. Nielsen, Andrew D. Bond and Jan O. Jeppesen Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . (Z)-methyl 2-chloro-3-(4-cyanophenyl)acrylate ÏàËÆ¶È:66.6% European Journal of Organic Chemistry 2011 1015-1022 Biocatalyzed Enantioselective Reduction of Activated C=C Bonds: Synthesis of Enantiomerically Enriched -Halo-¦Â-arylpropionic Acids Elisabetta Brenna, Francesco G. Gatti, Alessia Manfredi, Daniela Monti and Fabio Parmeggiani Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . H-Phe(3-CN)-OMe¡ÁHCl C11H12N2O2 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2011 19 7236-7243 The arginine mimicking ¦Â-amino acid ¦Â3hPhe(3-H2N-CH2) as S1 ligand in cyclotheonamide-based ¦Â-tryptase inhibitors Dennis Janke, Christian P. Sommerhoff, Norbert Schaschke Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . (Z)-Ethyl 3-(4-trifluoromethylphenylseleno)acrylate C12H11F3O2Se ÏàËÆ¶È:60% Tetrahedron 2012 68 10523-10529 Palladium-catalyzed vinylselenation of allenes Shin-ichi Fujiwara, Maiko Okuyama, Susumu Tsuda, Takanori Iwasaki, Hitoshi Kuniyasu, Nobuaki Kambe Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . Methyl 2-formylbenzoate 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 ̼Æ×Ä£Äâͼ 10 . 2-Nitro-3-thienylmethyltriphenylphosphonium bromide ÏàËÆ¶È:55.5% Canadian Journal of Chemistry 2008 86 668-675 Effect of base on alkyltriphenylphosphonium salts in polar aprotic solvents Julius N. Ngwendson, Cassandra M. Schultze, Jordan W. Bollinger, and Anamitro Banerjee Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . compound 6a C25H25BNP ÏàËÆ¶È:55.5% Tetrahedron Letters 2000 41 6143-6147 Addition of borane-protected secondary phosphines to imines. A route to protected mono-N-substituted-¦Á-aminophosphines Batia Ben-Aroya Bar-Nir, Moshe Portnoy Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . (5Z)-1,5,7-octatrien-4-ol C8H12O ÏàËÆ¶È:55.5% Organic letters 2000 2 3897-3899 Syntheses with Organoboranes. XI. Allylboration of Vinylic Epoxides with Allylic Dialkylboranes Marek Zaidlewicz and Marek P. Krzemi¨½ski Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . methyl (Z)-3-(4-chlorophenyl)-2-(mercaptomethyl)prope-noate C11H11ClO2S ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2009 46 23-27 A new route to allyl thiols and allyl thiocarbamates from Baylis-Hillman adducts Young-Gi Kim,Hee Nam Lim and Kee-Jung Lee Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . methyl 2-benzamidoacrylate C11H11NO3 ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2009 46 1235-1238 Novel and convenient to substituted imidazoles Yu-An Chang and Hsiang Chang Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 5-bromo-2,4-dichloro benzoic acid ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2007 44 273-275 An improved synthesis of 1-acetyl-1H-indol-3-yl acetates Juan C. Rodr¨ªguez-Dom¨ªnguez,Alexander Balbuzano-Deus,Miguel A. L¨®pez-L¨®pez,Juan C. Rodr¨ªguez-Dom¨ªnguez and Gilbert Kirsch Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . 1-(4-cyanobenzyl)-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]-decane bromide C14H18BrN5 ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2003 40 229-241 Preparation of a clinically investigated ras farnesyl transferase inhibitor Peter E. Maligres,Marjorie S. Waters,Steven A. Weissman,J. Christopher McWilliams,Stephanie Lewis,Jennifer Cowen,Robert A. Reamer,R. P. Volante,Paul J. Reider and David Askin Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . 7-loro-4-(hydroxyamino)-3-nitroquinolin-2(1H)-one C9H6ClN3O4 ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2003 40 617-623 Synthesis and biological properties of 4-substituted quinolin-2(1H)-one analogues Jae-Chul Jung,Seikwan Oh,Won-Ki Kim,Woo-Kyu Park,Jae Yang Kong and Oee-Sook Park Structure 13C NMR ̼Æ×Ä£Äâͼ 18 . compound 3g C11H8BrNO ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2000 37 15-24 Synthesis and nuclear magnetic resonance spectroscopic studies of 1-arylpyrroles Chang Kiu Lee, Jung Ho Jun and Ji Sook Yu Structure 13C NMR ̼Æ×Ä£Äâͼ 19 . 3-(1H-tetrazole-5-yl)benzonitrile ÏàËÆ¶È:55.5% Journal of Heterocyclic Chemistry 2010 47 913-922 Clay-catalyzed synthesis of 5-substituent 1-H-tetrazoles Alireza Najafi Chermahini, Abbas Teimouri, Fariborz Momenbeik, Amin Zarei, Zeinab Dalirnasab, Aseyeh Ghaedi and Mostafa Roosta Structure 13C NMR ̼Æ×Ä£Äâͼ 20 . dibenzo[b,f]thiepine-10,11-dione ÏàËÆ¶È:55.5% Heterocycles 2009 78 2489-2507 2,8-Dithia-dibenzo[e,h]azulenes and Their 8-Oxa Analogs. Synthesis and Anti-inflammatory Activity Ivana Ozimec Landek, Dijana Pešić, Predrag Novak, Barbara Stanić, Krunoslav Nujić, Mladen Merćep, and Milan Mesić Structure 13C NMR ̼Æ×Ä£Äâͼ 21 . Compound 8 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry Letters 1991 1 635-638 New stereospecific synthesis of (E,E,Z)- and (E,E,E)-10,12,14-hexadecatrienal sex pheromonal components of Manducta sexta Fr¨¦d¨¦rique Tellier Structure 13C NMR ̼Æ×Ä£Äâͼ 22 . Compound 9 ÏàËÆ¶È:55.5% Bioorganic & Medicinal Chemistry Letters 1991 1 635-638 New stereospecific synthesis of (E,E,Z)- and (E,E,E)-10,12,14-hexadecatrienal sex pheromonal components of Manducta sexta Fr¨¦d¨¦rique Tellier Structure 13C NMR ̼Æ×Ä£Äâͼ |

2Â¥2013-09-16 13:37:09














»Ø¸´´ËÂ¥