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liujie3214: ½ð±Ò+14, ¡ï¡ï¡ïºÜÓаïÖú, ·Ç³£¸Ðл¹þ 2015-04-05 21:35:50
1 .     2',3',5'-Triacetoxy-p-terphenyl
C24H20O6     ÏàËÆ¶È:64.7%
Bioscience, Biotechnology, and Biochemistry          2006          70          2998-3003
Syntheses of Naturally Occurring Terphenyls and Related Compounds
Yusuke SAWAYAMA, Takashi TSUJIMOTO, Kumi SUGINO, Toshio NISHIKAWA, Minoru ISOBE and Hirokazu KAWAGISHI
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
2 .     (E)-3-(3-methylbenzylidene)-5-phenylpiperidine-2,6-dione
C19H17NO2     ÏàËÆ¶È:64.7%
European Journal of Organic Chemistry          2010                   5650-5658
A Facile Synthesis of Substituted Indenones and Piperidine-2,6-diones from the Baylis¨CHillman Acetates
Deevi Basavaiah and Dandamudi V. Lenin
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
3 .     1-[4-(3,4-dimethylphenyl)-4-oxobutyl]-4-(diphenylmethyl)piperazine
C29H34N2O     ÏàËÆ¶È:63.1%
Bioorganic & Medicinal Chemistry          2014          22          95-104
A highly predictive 3D-QSAR model for binding to the voltage-gated sodium channel: Design of potent new ligands
Congxiang Zha, George B. Brown, Wayne J. Brouillette
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
4 .     (1,3-diphenylbut-3-enyl)(p-tolyl)sulfane
C23H22S     ÏàËÆ¶È:62.5%
Chinese Chemical Letters          2011          22          1179-1182
A mild and highly efficient one-pot three-component reaction for carbon¨Csulfur bond formation catalyzed by potassium tert-butoxide
Barahman Movassagh, Amir Rakh
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
5 .     (E)-3-Benzylidene-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
    ÏàËÆ¶È:62.5%
Molecules          2012          17          571-583
A Facile Solvent Free Claisen-Schmidt Reaction: Synthesis of ,'-bis-(Substituted-benzylidene)cycloalkanones and ,'-bis-(Substituted-alkylidene)cycloalkanones
A. F. M. Motiur Rahman, Roushown Ali, Yurngdong Jahng and Adnan A. Kadi
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
6 .     5-(1-Benzyl-5-methyl-3-oxido-1H-imidazol-4-yl)-4-butyl-2,4-dihydro-3H-1,2,4-triazole-3-thione
C17H21N5OS     ÏàËÆ¶È:62.5%
Helvetica Chimica Acta          2012          95          404-414
Synthesis of Bis-Heterocyclic 1H-Imidazole 3-Oxides from 3-Oxido-1H-imidazole-4-carbohydrazides
Adam Marek Pieczonka,Grzegorz Mloston
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
7 .     N-(3,4-dimethylbenzyl)benzamide
C16H17NO     ÏàËÆ¶È:62.5%
Tetrahedron          2012          68          2342-2348
One-pot stibine modified Co2(CO)8 catalyzed reductive N-alkylation of primary amides with carbonyl compounds
Laura Rubio-P¨¦rez, Pankaj Sharma, F. Javier P¨¦rez-Flores, Luis Velasco, J. Luis. Arias, Armando Cabrera
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
8 .     squalestatin S5
    ÏàËÆ¶È:62.5%
The Journal of Antibiotics          1994          47          740-754
THE SQUALESTATINS, NOVEL INHIBITORS OF SQUALENE SYNTHASE PRODUCED BY A SPECIES OF Phoma V. MINOR METABOLITES
WILLIAM M. BLOWS, GRAHAM FOSTER, STEPHEN J. LANE, DAVID NOBLE, JOHN E. PIERCEY, PHILIP J. SIDEBOTTOM, GRAHAM WEBB
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
9 .     squalestatin H5
    ÏàËÆ¶È:62.5%
The Journal of Antibiotics          1994          47          740-754
THE SQUALESTATINS, NOVEL INHIBITORS OF SQUALENE SYNTHASE PRODUCED BY A SPECIES OF Phoma V. MINOR METABOLITES
WILLIAM M. BLOWS, GRAHAM FOSTER, STEPHEN J. LANE, DAVID NOBLE, JOHN E. PIERCEY, PHILIP J. SIDEBOTTOM, GRAHAM WEBB
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
10 .     N-[(2,6-dimethylphenylamino)phenylmethylene]-4-methylbenzamide
C23H22N2O     ÏàËÆ¶È:62.5%
European Journal of Organic Chemistry          2011                   861-877
Synthesis, Structures, and Aggregation Properties of N-Acylamidines
Christof Wigbers, Jörg Prigge, Zhongchen Mu, Roland Fröhlich, Lifeng Chi and Ernst-Ulrich W¨¹rthwein
Structure      13C NMR    Structure & 13C NMR     Ì¼Æ×Ä£Äâͼ
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