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1 .     5-amino-3-tert-butyl-6-cyano-1H-2,3-dihydroimidazo[4,5-b]pyrazin-2-one
C10H12N6O     ÏàËÆ¶È:62.5%
Journal of Heterocyclic Chemistry          2000          37          1151-1156
New syntheses and spectral properties of pteridine-related heterocycles from 2,5-diamino-3,6-dicyanopyrazine
Kazuko Shirai, Koushi Fukunishi, Atsushi Yanagisawa, Hiroshi Takahashi and Masaru Matsuoka
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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2 .     compound 12
    ÏàËÆ¶È:62.5%
Tetrahedron Letters          2002          43          959-961
A convenient synthesis of (Z)-1-chloro-1-alkenes and (Z)-1-chloro-2-alkoxy-1-alkenes
Rachid Baati, D.K. Barma, U.Murali Krishna, Charles Mioskowski, J.R. Falck
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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3 .     tichocarpol A
C9H10O7S     ÏàËÆ¶È:57.1%
Journal of Natural Products          2004          67          1764-1766
Tichocarpols A and B, Two Novel Phenylpropanoids with Feeding-Deterrent Activity from the Red Alga Tichocarpus crinitus
Takahiro Ishii, Tatsufumi Okino, Minoru Suzuki, and Yuji Machiguchi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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4 .     4-(3-Hydroxy-propenyl)-phenol
C9H10O2     ÏàËÆ¶È:57.1%
Acta Botanica Yunnanica          2005          27(2)          217-222
A New Sesquilignan from Tsuga dumosa
ZHAO You-Xing, LI Cheng-Sen, LUO Xiao-Dong,LIU Yu-Qing,ZHOU Jun
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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5 .     1,5-Bis(phenyl selanyl)pentane
    ÏàËÆ¶È:57.1%
Canadian Journal of Chemistry          2009          87          678-683
On the reactivity of indium(III) benzenechalcogenolates (chalcogen = sulfur and selenium) towards organyl halides for the synthesis of organyl phenyl chalcogenides
Clovis Peppe and Li¨¦rson Borges de Castro
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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6 .     methyl vinyl ketone
    ÏàËÆ¶È:57.1%
Canadian Journal of Chemistry          2006          84          762-770
Indium(I) iodide promoted cleavage of dialkyl disulfides - Application of the Michael addition of thiolate anions to conjugated carbonyl compounds and regioselective ring opening of epoxides
Brindaban C. Ranu and Tanmay Mandal
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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7 .     5-Phenylisoxazole
C9H7NO     ÏàËÆ¶È:57.1%
Journal of Heterocyclic Chemistry          2008          45          879-885
Reaction of ¦Â-dimethylaminovinyl ketones with hydroxylamine: A simple and useful method for synthesis of 3-and 5-substituted isoxazoles
Fernanda A. Rosa,Pablo Machado,Helio G. Bonacorso,Nilo Zanatta and Marcos A. P. Martins
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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8 .     5-phenyl-3-(trifluoromethyl)isoxazole
    ÏàËÆ¶È:57.1%
Journal of Heterocyclic Chemistry          2005          42          1253-1255
Synthesis of 3-phenyl-5-(trifluoromethyl)isoxazole and 5-phenyl-3-(trifluoromethyl)isoxazole
James W. Pavlik,Jennifer A. Lowell and Vuthichai Ervithayasuporn
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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9 .     4-benzyl-1H-pyrazole-3,5-diamine
C10H12N4     ÏàËÆ¶È:57.1%
Heterocycles          2008          75          1371-1383
Studies with Malononitrile Derivatives: Synthesis and Reactivity of 4-Benzylpyrazole-3, 5-diamine, 4-Benzylisoxazole-3, 5-diamine and Thiazolidin-3-phenylpropanenitrile
Saleh Mohammed Al-Mousawi, Moustafa Sherief Moustafa, and Mohamed Hilmy Elnagdi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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10 .     2,2,2-trifluoro-2'-nitroacetophenone
    ÏàËÆ¶È:57.1%
Heterocycles          2004          63          373-382
Synthesis of 1H-Indazoles by Reductive Cyclization of o-Nitro-ketoximes
David K. O'Dell and Kenneth M. Nicholas*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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11 .     3-chloro-4-phenylethynyl-1,2,5-thiadiazole
C10H5N2ClS     ÏàËÆ¶È:57.1%
Heterocycles          2003          60          29-45
The Palladium-catalyzed Cross-coupling reactions of 3-Chloro-4-halogeno-1,2,5-thiadiazoles
Alain Merschaert* and Hugo J. Gorissen
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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12 .     N-Methyl-3-acetyl pyrrole
C7H9NO     ÏàËÆ¶È:57.1%
Molecules          2010          15          2972-2979
A Mild and Facile One-Pot Synthesis of N-Methyl-3-Acyl-Pyrroles
Hassan Valizadeh and Ashraf Fakhari
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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13 .     N,N-dimethyltyramine
    ÏàËÆ¶È:57.1%
Chinese Traditional and Herbal Drugs          2007          38          652-655
Cytotoxic constituents from red alga Gymnogongrus flabelliformis
YUAN Zhao-hui; HAN Li-jun; FAN Xiao; LI Shuai; SHI Da-yong; SUN Jie; YANG Yong-chun; SHI Jian-gong
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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14 .     compound 11a
    ÏàËÆ¶È:57.1%
Tetrahedron Letters          2002          43          7365-7368
Copper-catalyzed amidations of bromo substituted furans and thiophenes
Kenneth R Crawford, Albert Padwa
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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15 .     compound 6
    ÏàËÆ¶È:57.1%
Tetrahedron Letters          2004          45          3789-3791
From 1,4-diketones to N-vinyl derivatives of 3,3'-bipyrroles and 4,8-dihydropyrrolo[2,3-f]indole in just two preparative steps
Boris A. Trofimov, Alexey B. Zaitsev, Elena Yu. Schmidt, Alexander M. Vasil'tsov, Al'bina I. Mikhaleva, Igor' A. Ushakov, Alexander V. Vashchenko, Nadezhda V. Zorina
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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16 .     2-Imidazolo-1-ylmethylene-malononitrile
C7H4N4     ÏàËÆ¶È:57.1%
Zeitschrift f¨¹r Naturforschung B          2005          60          106-112
Base Catalyzed Synthesis of Novel Fused-Imidazoles from N-Vinyl-1H-imidazole
A. A. Aly
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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17 .     1,3-Dimethoxyimidazolium phenyltrifluoroboronate
    ÏàËÆ¶È:57.1%
Zeitschrift f¨¹r Naturforschung B          2007          62          295-308
N,N'-Di(alkyloxy)imidazolium Salts: New Patent-free Ionic Liquids and NHC Precatalysts
G. Laus, A. Schwärzler, P. Schuster, G. Bentivoglio, M. Hummel, K. Wurst, V. Kahlenberg, T. Lörting, J. Sch¨¹tz, P. Peringer, G. Bonn, G Nauer, and H. Schottenberger
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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18 .     2-[(4-Chlorophenyl)hydrazono]malonaldehyde monooxime
C9H8ClN2O2     ÏàËÆ¶È:57.1%
Zeitschrift f¨¹r Naturforschung B          2007          62          529-536
Studies with 2-(Arylhydrazono)aldehydes: Synthesis and Chemical Reactivity of Mesoxalaldehyde 2-Arylhydrazones and of Ethyl 2-Arylhydrazono-3-oxopropionates
S. Makhseed, H. M. E. Hassaneen, and M. H. Elnagdi
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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19 .     compound 8
C52H68N4O8     ÏàËÆ¶È:57.1%
Heterocycles          2002          57          1091-1099
One-Step Synthesis of Optically Active Cyclic Polyamines Containing Helicene
Shinobu Honzawa, Shinya Chiba, Hitoshi Okubo, and Masahiko Yamaguchi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ

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20 .     compound 9
    ÏàËÆ¶È:57.1%
Heterocycles          2002          57          1091-1099
One-Step Synthesis of Optically Active Cyclic Polyamines Containing Helicene
Shinobu Honzawa, Shinya Chiba, Hitoshi Okubo, and Masahiko Yamaguchi*
Structure      13C NMR   Ì¼Æ×Ä£Äâͼ
2Â¥2012-09-18 15:45:40
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