| ²é¿´: 423 | »Ø¸´: 2 | ||
yulin07002½ð³æ (СÓÐÃûÆø)
|
[ÇóÖú]
΢Æ×Êý¾ÝÇóÖú£¡
|
|
Âé·³¸÷λ´óÏÀ°ïÎÒ²éÒ»ÏÂÕâ¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý£¬Ð»Ð»¡£»¯ºÏÎï̼Æ×Êý¾ÝÈçÏ£º 14.1, 22.7, 26.0, 28.9, 29.2, 29.3, 31.8, 65.2, 68.5, 101.5, 107.8, 128.3, 128.3, 128.9, 128.9, 131.4, 135.2, 138.3, 165.8, 188.5, 200.1. |
» ²ÂÄãϲ»¶
ÉúÎïѧѧ˶Çóµ÷¼Á£º351·ÖÒ»Ö¾Ô¸ÄϾ©Ê¦·¶´óѧÉúÎïѧרҵ
ÒѾÓÐ5È˻ظ´
Çóµ÷¼Á£¬Ò»Ö¾Ô¸ÏÃÃÅ´óѧ£¬ÉúÎïÓëÒ½Ò©£¬×Ü·Ö272£¬±¾¿Æ211
ÒѾÓÐ5È˻ظ´
µ÷¼Á
ÒѾÓÐ9È˻ظ´
070300»¯Ñ§Ñ§Ë¶311·ÖÇóµ÷¼Á
ÒѾÓÐ11È˻ظ´
Ò»Ö¾Ô¸±±½»´ó²ÄÁϹ¤³Ì×Ü·Ö358Çóµ÷¼Á
ÒѾÓÐ7È˻ظ´
308Çóµ÷¼Á
ÒѾÓÐ12È˻ظ´
0703»¯Ñ§
ÒѾÓÐ18È˻ظ´
ÉúÎïѧ308·ÖÇóµ÷¼Á£¨Ò»Ö¾Ô¸»ª¶«Ê¦´ó£©
ÒѾÓÐ5È˻ظ´
292Çóµ÷¼Á
ÒѾÓÐ4È˻ظ´
286Çóµ÷¼Á
ÒѾÓÐ10È˻ظ´
» ±¾Ö÷ÌâÏà¹Ø¼ÛÖµÌùÍÆ¼ö£¬¶ÔÄúͬÑùÓаïÖú:
΢Æ×Êý¾ÝÇóÖú....!
ÒѾÓÐ3È˻ظ´
΢Æ×ÕæµÄͦ²»´íµÄ£¡
ÒѾÓÐ4È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ4È˻ظ´
΢Æ×Êý¾ÝÇóÖú¡ª¡ªÈý¸ö»¯ºÏÎï лл£¡
ÒѾÓÐ8È˻ظ´
΢Æ×ÇóÖú£¬Ð»Ð»
ÒѾÓÐ5È˻ظ´
ÇóÖúÁ½¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ3È˻ظ´
ÇóÖúÒ»¸ö»¯ºÏÎïµÄ΢Æ×Êý¾Ý
ÒѾÓÐ4È˻ظ´
¼±Ç󣡣¡£¡£¡Bulletin of the Korean Chemical SocietyͶ¸å¸ñʽÎÊÌâ
ÒѾÓÐ13È˻ظ´
΢Æ×Êý¾Ý²éѯÇóÖú
ÒѾÓÐ3È˻ظ´
ÇóÖú΢Æ×Êý¾Ý²éѯ
ÒѾÓÐ8È˻ظ´
ÇóÖúͨ¹ý΢Æ×²éѯ»¯ºÏÎï½á¹¹
ÒѾÓÐ4È˻ظ´
Çó´óϺ²é΢Æ×£¬Íò·Ö¸Ðл°¡£¡£¡£¡
ÒѾÓÐ3È˻ظ´
¹òÇóÄÜÓÃ΢Æ×Êý¾Ý¿âµÄ³æ×ÓÃÇ£¬°ïæ²éÒ»ÏÂ̼Æ×Êý¾Ý£¬±¾ÈËËÍ6¸ö½ð±Ò£¡£¡£¡
ÒѾÓÐ7È˻ظ´
[ÇóÖú]ÄÄλºÃÈËѧУ¿ÉÒÔʹÓÃ΢Æ×Êý¾Ý¿â£¬°ïÎÒ¼ìË÷¼¸¸ö»¯ºÏÎïµÄĸºË¡£Ð»Ð»£¡
ÒѾÓÐ4È˻ظ´
Ц¶à»á»³ÔÐ
Ìú¸Ëľ³æ (ÖøÃûдÊÖ)
- Ó¦Öú: 1216 (½²Ê¦)
- ½ð±Ò: 9788.1
- É¢½ð: 610
- ºì»¨: 40
- ɳ·¢: 3
- Ìû×Ó: 2723
- ÔÚÏß: 1284.6Сʱ
- ³æºÅ: 2010893
- ×¢²á: 2012-09-18
- ÐÔ±ð: GG
- רҵ: ÌìÈ»Óлú»¯Ñ§
¡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
yulin07002(À±±ÊvСдú·¢): ½ð±Ò+20, ½±ÀøÓ¦Öú£¬Ð»Ð» 2013-12-02 11:34:21
¸Ðл²ÎÓ룬ӦÖúÖ¸Êý +1
yulin07002(À±±ÊvСдú·¢): ½ð±Ò+20, ½±ÀøÓ¦Öú£¬Ð»Ð» 2013-12-02 11:34:21
|
²éѯ½á¹û£º¹²²éµ½825¸ö»¯ºÏÎï(²éѯ½á¹û½ö¹©²Î¿¼) 1 . 2-Hydroxy-(4-octyloxy)benzophenone ÏàËÆ¶È:85.7% Chemistry of Natural Compounds 2005 41 101-102 PHENOLIC COMPOUNDS FROM Pinus sibirica SHELLS E. A. Khamidullina, M. Purevdash I. V. Ushakov,O. V. Neretina, and S. A. Medvedeva1 Structure 13C NMR ̼Æ×Ä£Äâͼ 2 . compound 3 C20H24N2O3 ÏàËÆ¶È:70% Tetrahedron 2012 68 9200-9205 Tunable conformation and stability of amidourea-based hydrogen-bonded heteroduplexes Wei-Jun Chu, Chuan-Feng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 3 . n-octyl N-acetyl-2,3-aziridino-5-O-benzoyl-2,3-dideoxy-¦Â-D-ribofuranoside C22H31NO5 ÏàËÆ¶È:70% Tetrahedron 2013 69 4276-4284 Glycosylations with 2,3-aziridinofuranose derivatives Md Faiaz Ahmed, Todd L. Lowary Structure 13C NMR ̼Æ×Ä£Äâͼ 4 . 3-Octanoylamino benzoic acid benzyl ester C22H27NO3 ÏàËÆ¶È:65% Archiv der Pharmazie 2008 341 386-392 Synthesis of Platensimycin Analogues and Their Antibiotic Potency J¨¹rgen Krauss, Veronika Knorr, Vera Manhardt, Stefanie Scheffels and Franz Bracher Structure 13C NMR ̼Æ×Ä£Äâͼ 5 . 1-(4-bromophenyl)-5-methyl-2-octylpyrazolium iodide C18H25BrN2 ÏàËÆ¶È:65% European Journal of Organic Chemistry 2010 4296-4305 Rearrangements of N-Heterocyclic Carbenes of Pyrazole to 4-Aminoquinolines and Benzoquinolines Andrij Dreger, Rafael Cisneros Camuña, Niels M¨¹nster, Tibor Andr¨¢s Rokob, Imre P¨¢pai and Andreas Schmidt Structure 13C NMR ̼Æ×Ä£Äâͼ 6 . benzyl 6-O-undecyl-4-deoxy-¦Á-D-lyxo-pyranoside C24H40O5 ÏàËÆ¶È:65% Bioorganic & Medicinal Chemistry 2013 21 6554-6564 Synthesis and anti-tumor activity of carbohydrate analogues of the tetrahydrofuran containing acetogenins Stewart Bachan, K.A. Tony, Akira Kawamura, Diego Montenegro, Anjali Joshi, Himanshu Garg, David R. Mootoo Structure 13C NMR ̼Æ×Ä£Äâͼ 7 . compound B3 C43H58N6O6 ÏàËÆ¶È:63.6% Tetrahedron 2012 68 9200-9205 Tunable conformation and stability of amidourea-based hydrogen-bonded heteroduplexes Wei-Jun Chu, Chuan-Feng Chen Structure 13C NMR ̼Æ×Ä£Äâͼ 8 . 2-Decanoylamino-pentanedioic acid 5-allyl ester 1-benzyl ester C25H37NO5 ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry 1997 5 165-177 Combinatorial synthesis and biological evaluation of Library of small-molecule Ser/Thr-protein phosphatase inhibitors Peter Wipf, April Cunningham, Robert L. Rice, John S. Lazo Structure 13C NMR ̼Æ×Ä£Äâͼ 9 . 2-Decanoylamino-pentanedioic acid 5-allyl ester 1-benzyl ester C25H37NO5 ÏàËÆ¶È:61.9% Bioorganic & Medicinal Chemistry 2000 8 1451-1466 Identification of new Cdc25 dual specificity phosphatase inhibitors in a targeted small molecule array Alexander P Ducruet, Robert L Rice, Kenji Tamura, Fumiaki Yokokawa, Shiho Yokokawa, Peter Wipf, John S Lazo Structure 13C NMR ̼Æ×Ä£Äâͼ 10 . Octyl 5-methyl-1-(2-(phenylselanyl)phenyl)-1H-1,2,3-triazole-4-carboxylate C24H28N3O2Se ÏàËÆ¶È:61.9% Tetrahedron 2012 68 10456-10463 Synthesis of arylselanyl-1H-1,2,3-triazole-4-carboxylates by organocatalytic cycloaddition of azidophenyl arylselenides with ¦Â-keto-esters Nat¨¢lia Seus, Loren C. Gonçalves, Anna M. Deobald, Lucielli Savegnago, Diego Alves, M¨¢rcio W. Paixão Structure 13C NMR ̼Æ×Ä£Äâͼ 11 . 2-Benzamido-5-(heptadec-8-enyl)-1 ,3,4-thiadiazole C26H39OS ÏàËÆ¶È:60% Chinese Chemical Letters 2008 19 1427-1430 Synthesis and evaluation of in vitro antibacterial activity of novel 2,5-disubstituted-1£¬3£¬4-thiadiazoles from fatty acids Mudasir R£®Banday,Abdul Rauf Structure 13C NMR ̼Æ×Ä£Äâͼ 12 . N-alkyl-quinolinium C20H30N ÏàËÆ¶È:60% Molecules 2002 7 320-330 Synthesis and Spectroscopic Characterisation of N-Alkyl Quaternary Ammonium Salts Typical Precursors of Cyanines A. C. Pardal, S. S. Ramos, P. F. Santos, L. V. Reis and P. Almeida Structure 13C NMR ̼Æ×Ä£Äâͼ 13 . 1,4-Bis(4-nonyloxyphenyl)-6,7-dimethylanthraquinone C46H57O4 ÏàËÆ¶È:60% Molecules 2009 14 1013-1031 Brominated Thiophenes as Precursors in the Preparation of Brominated and Arylated Anthraquinones Thies Thiemann, Yasuko Tanaka and Jesus Iniesta Structure 13C NMR ̼Æ×Ä£Äâͼ 14 . 1-Benzhydryl-3-decyl imidazol-3-ium bromide C26H34N2 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2011 19 4868-4875 LuxR dependent quorum sensing inhibition by N, N'-disubstituted imidazolium salts Mohamad Sabbah, Laurent Soul¨¨re, Sylvie Reverchon, Yves Queneau, Alain Doutheau Structure 13C NMR ̼Æ×Ä£Äâͼ 15 . 1-Benzhydryl-3-dodecyl imidazol-3-ium bromide C28H40N2 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2011 19 4868-4875 LuxR dependent quorum sensing inhibition by N, N'-disubstituted imidazolium salts Mohamad Sabbah, Laurent Soul¨¨re, Sylvie Reverchon, Yves Queneau, Alain Doutheau Structure 13C NMR ̼Æ×Ä£Äâͼ 16 . compound 4e C24H31N3 ÏàËÆ¶È:60% Heterocycles 2009 78 645-655 Copper(I)-Catalyzed Direct Arylation of 1,4-Disubstituted 1,2,3-Triazoles with Aryl Iodides Shin-ichi Fukuzawa, Eiji Shimizu, and Kenichi Ogata Structure 13C NMR ̼Æ×Ä£Äâͼ 17 . compound 6d C26H31FeN3 ÏàËÆ¶È:60% Heterocycles 2009 78 645-655 Copper(I)-Catalyzed Direct Arylation of 1,4-Disubstituted 1,2,3-Triazoles with Aryl Iodides Shin-ichi Fukuzawa, Eiji Shimizu, and Kenichi Ogata Structure 13C NMR ̼Æ×Ä£Äâͼ |
2Â¥2013-12-02 08:17:09
yulin07002
½ð³æ (СÓÐÃûÆø)
- Ó¦Öú: 0 (Ó×¶ùÔ°)
- ½ð±Ò: 902
- É¢½ð: 20
- ºì»¨: 1
- Ìû×Ó: 88
- ÔÚÏß: 43.5Сʱ
- ³æºÅ: 1297952
- ×¢²á: 2011-05-17
- רҵ: ÌìȻҩÎﻯѧ
3Â¥2013-12-02 11:31:23














»Ø¸´´ËÂ¥
5