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pq5341

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13C NMR (75 MHz, CDCl3) δ =106.84, 111.03, 113.66, 119.25, 124.13, 124.61, 131.84, 134.74, 138.58, 138.70, 141.14, 141.48, 146.86, 147.24, 155.15.
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yangyinhe

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pq5341(卓越_先锋代发): 金币+20, ok 2015-04-13 08:57:20
1 .     (1'E,5'E)-5-(2',6'-dimethylocta-1',5',7'-trienyl)furan-3-carboxylic acid
    相似度:66.6%
Chinese Journal of Natural Medicines          2003          1          193-195
Studies on the Chemical Constituents of the Soft Coral Sinularia sp
JIA Rui; GUO Yue-Wei; HOU Hui-Xin; Mollo Ernes to; Cimino Guido
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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2 .     (1'E,5'E)-2-(2',6'-dimethylocta-1',5',7'-trienyl)-4-furoic acid
C15H18O3     相似度:66.6%
Tetrahedron          1996          52          4245-4256
Two practical syntheses of an anti-inflammatory sesquiterpene furoic acid from Sinularia spp
David H. Williams, D. John Faulkner
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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3 .     4-(2-bromopyridin-3-yl)-4,5-dihydropyrrolo[1,2-a]quinoxaline
C16H12BrN3     相似度:66.6%
European Journal of Organic Chemistry          2011                   6998-7010
Lewis Acid-Catalyzed Selective Synthesis of Diversely Substituted Indolo- and Pyrrolo[1,2-a]quinoxalines and Quinoxalinones by Modified Pictet–Spengler Reaction
Akhilesh K. Verma, Rajeev R. Jha, V. Kasi Sankar, Trapti Aggarwal, Rajendra P. Singh and Ramesh Chandra
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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4 .     6-chloro-4'-methyl-2-(N-phenylamino)quinoline
C16H13N2Cl     相似度:66.6%
Journal of Heterocyclic Chemistry          2013          50          1049-1063
Effect of Substituents in the Syntheses of Phenyl-Substituted Dibenzonaphthyridines
Manickam Manoj and Karnam Jayaramapillai Rajendra Prasad
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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5 .     (1'E,5'E)-5-(2',6'-Dimethylocta-1',5',7'-trienyl)furnn-3-carboxylic acid
C15H18O3     相似度:66.6%
Australian Journal of Chemistry          1983          36          371-376
Studies of Australian soft corals. XXXI. Novel furanosesquiterpenes from several sinularian soft corals (Coelenterata, Octocorallia, Alcyonacea)
BF Bowden, JC Coll, Silva ED de and Costa MSL de
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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6 .     2-(4-(methylsulfonyl)phenyl)-N-(2-pyridinyl)-imidazo[1,2-a]pyridin-3-amine
NC19H16N4O2S     相似度:64.7%
Bioorganic & Medicinal Chemistry          2009          17          74-84
Discovery of novel analgesic and anti-inflammatory 3-arylamine-imidazo[1,2-a]pyridine symbiotic prototypes
Renata B. Lacerda, Cleverton K.F. de Lima, Leandro L. da Silva, Nelilma C. Romeiro, Ana Luisa P. Miranda, Eliezer J. Barreiro, Carlos A.M. Fraga
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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7 .     (3-fluoro-2-(pyridin-2-yloxy)phenyl)(4-methoxyphenyl)methanone
C19H14FNO3     相似度:64.7%
Tetrahedron          2013          69          6552-6559
Pd-catalyzed oxidative acylation of 2-phenoxypyridines with alcohols via C–H bond activation
Minyoung Kim, Satyasheel Sharma, Jihye Park, Mirim Kim, Yeonhee Choi, Yukyoung Jeon, Jong Hwan Kwak, In Su Kim
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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8 .     2-[2-(5(6)-methyl)benzimidazolyl)-3-(2-chloro-5-nitro-phenyl)acrylonitrile
C17H11ClN4O2     相似度:62.5%
Bioorganic & Medicinal Chemistry          2011          19          6329-6339
Novel biologically active nitro and amino substituted benzimidazo[1,2-a]quinolines
Nataša Perin, Lidija Uzelac, Ivo Piantanida, Grace Karminski-Zamola, Marijeta Kralj, Marijana Hranjec
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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9 .     Eudistomin Y2
C18H9N2O2Br     相似度:62.5%
Marine Drugs          2013          11          1427-1439
Total Synthesis and Biological Activity of Marine Alkaloid Eudistomins Y1–Y7 and Their Analogues
Huijuan Jin, Puyong Zhang, Krikor Bijian, Sumei Ren, Shengbiao Wan, Moulay A. Alaoui-Jamali and Tao Jiang
Structure      13C NMR    Structure & 13C NMR     碳谱模拟图

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10 .     9-(4-Nitrophenylsulfanylmethylidene)-8,9-dihydro-5H-pyrido[4,3-e][1,3]thiazolo[3,2-a]pyrimidin-5-one
C16H10N4O3S2     相似度:60%
Russian Journal of Organic Chemistry          2014          50          858−863
Fused Pyrimidine Systems: XIV.* Reaction of 2-Alkenyl(alkynyl)sulfanylpyrido[3,4-d]pyrimidin-4(3H)-ones with Arylsulfanyl Chlorides
I. V. Dyachenko, A. I. Vas’kevich, R. I. Vas’kevich, and M. V. Vovk
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