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13.71, 14.49, 16.44, 16.82, 17.27, 23.10, 46.02, 106.05, 107.36, 119.13, 120.27, 124.28, 128.14, 128.50, 138.89, 141.41, 143.62, 153.80, 158.68, 164.04, 164.41, 164.82, 165.31

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331456351: ½ð±Ò+10, ¡ï¡ï¡ïºÜÓаïÖú 2013-08-20 22:15:08
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1 .     4¦Â-Cinnamoyloxy-7¦Á-bydroperoxy-1¦Â-hydroxyeudesm-8-ene
    ÏàËÆ¶È:52.1%
Phytochemistry          1993          34          737-742
Sesquiterpenes from Brintonia discoidea
Lu Tiansheng, David Vargas, Nikolaus H. Fischer
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2 .     5-ethyl-2-methylthio-6-{3-[(5-ethyl-2-piperidinyl-pyrimid-in-4(1H,3H)-yl)methyl]benzyl}pyrimidine-2,4(1H,3H)-one
C26H33N5O2S     ÏàËÆ¶È:52.1%
Journal of Heterocyclic Chemistry          2007          44          381-387
Synthesis and anti-HIV-1 activity of 1,3-phenylene bis-uracil analogues of MKC-442
Youssef L. Aly,Erik B. Pedersen,Paolo La Colla and Roberta Loddo
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
3 .     4-(2,6-difluorophenyl)-6-(1,2,3,4-tetrahydronaphthalen-6-yl)-2-oxo-1,2-dihydropyridine-3-carboxamide
C22H18F2N2O2     ÏàËÆ¶È:52.1%
Molecules          2012          17          4717-4732
Article: Synthesis, Molecular Docking and Preliminary in-Vitro Cytotoxic Evaluation of Some Substituted Tetrahydro-naphthalene (2',3',4',6'-Tetra-O-Acetyl-¦Â-D-Gluco/-Galactopyranosyl) Derivatives
Maha S. Al-Mutairi, Ebtehal S. Al-Abdullah, Mogedda E. Haiba, Mohammed A. Khedr and Wafaa A. Zaghary
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
4 .     tetracenomycin A2
C19H12O6     ÏàËÆ¶È:52.1%
The Journal of Antibiotics          1988          41          1066-1073
METABOLIC PRODUCTS OF MICROORGANISMS. 249 TETRACENOMYCINS B3 AND D3, KEY INTERMEDIATES OF THE ELLORAMYCIN AND TETRACENOMYCIN C BIOSYNTHESIS
JURGEN ROHR, SUSANNE EICK, AXEL ZEECK, PETER REUSCHENBACH, HANS ZÄHNER, HANS-PETER FIEDLER
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
5 .     diethyl 2-{[(9H-fluoren-9-yl)methoxy]carbonyloxyimino}malonate
C22H21NO7     ÏàËÆ¶È:52.1%
European Journal of Organic Chemistry          2010                   3275-3280
Oxime Carbonates: Novel Reagents for the Introduction of Fmoc and Alloc Protecting Groups, Free of Side Reactions
Sherine N. Khattab, Ramon Subir¨®s-Funosas, Ayman El-Faham and Fernando Albericio
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
6 .     3-(4-nitrophenyl)-2,5,5-trimethyl-9a-methylsulfanyl-9-phenoxy-4,5,6,8,9,9a-hexahydro-3H-azeto[1,2-a] pyrrolo[3,2-c]azepin-8-one
C26H27N3O4S     ÏàËÆ¶È:50%
Heterocycles          2000          53          557-570
Synthesis of the New Triheterocyclic System C3N-C4N-C6N. 3-Aryl-2,5,5-trimethyl-9a-methylsulfanyl-9-phenoxy-4,5,6,8,9,9a-hexahydro-3H-azeto[1,2-a]pyrrolo[3,2-c]azepin-8-ones
Roberto Mart¨ªnez,* Jos¨¦ Gustavo Avila-Z¨¢rraga, Gema L¨®pez-L¨®pez, and V¨ªctor Oswaldo Nava-Salgado
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
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