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31.48,106.97,108.97,109.21,128.66,136.57,152.72,160.39,163.09,186.55
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namujila: 金币+10, ★★★★★最佳答案 2013-02-22 12:43:12
PSA: 金币+1, 辛苦 2013-02-22 12:48:23
1 .     methyl 2-(5'-tetrazolyl)-6-methylfuro[2,3-b]pyrrole-5-carboxylate
C10H9N5O3     相似度:60%
Molecules          1997          2          69-79
Synthesis and Reactions of Furo[2, 3-b]pyrroles
Alzbeta Krutosikova, C. A. Ramsden, Miloslava Dandarova and Antonin Lycka
Structure      13C NMR   碳谱模拟图
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2 .     2-Amino-4-(benzyloxy)-8-methylpteridin-7(8H)-one 5-Oxide
C14H13N5O3     相似度:50%
Helvetica Chimica Acta          2009          92          588-606
Acylation of a 6-(Methylamino)-5-nitrosopyrimidine and 1,3-Dipolar Cycloaddition of an 8-Methylisoxanthopterin N(5)-Oxide. Synthesis of C(6),N(8)-Disubstituted Isoxanthopterins
Thomas Steinlin, Andrea Vasella
Structure      13C NMR   碳谱模拟图
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3 .     compound 3a
    相似度:50%
Chinese Chemical Letters          2007          18          1431-1435
Knoevenagel condensation of α,β —unsaturated aromatic aldehydes with barbituric acid under non—catalytic and solvent—free conditions
herkupally Sanjeeva Reddy,Adki Nagaraj
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

4 .     methyl 2-formyl-6-methylfuro[2,3-b]pyrrole-5-carboxylate
C10H9NO4     相似度:50%
Molecules          1997          2          69-79
Synthesis and Reactions of Furo[2, 3-b]pyrroles
Alzbeta Krutosikova, C. A. Ramsden, Miloslava Dandarova and Antonin Lycka
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

5 .     5-Methoxycarbonyl-6-methylfuro[2,3-b]pyrrole-2-carbaldehyde dimethylhydrazone
C12H15N3O3     相似度:50%
Molecules          1997          2          69-79
Synthesis and Reactions of Furo[2, 3-b]pyrroles
Alzbeta Krutosikova, C. A. Ramsden, Miloslava Dandarova and Antonin Lycka
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

6 .     compound 19n
    相似度:50%
Bioorganic & Medicinal Chemistry Letters          2011          21          3002-3006
Discovery of piperidinyl aminopyrimidine derivatives as IKK-2 inhibitors
Sora Kim ,Jin Kyo Jung ,Hyo Seon Lee , Youngjae Kim ,Jiyoon Kim, Kihang Choi , Du-Jong Baek ,Bongjin Moon, Kwang-Seok Oh , Byung Ho Lee , Kye Jung Shin, Ae Nim Pae , Ghilsoo Nam,Eun Joo Roh, Yong Seo Cho, Hyunah Choo
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

7 .     6-hydroxy-7-methoxy-4-trifluoromethylquinolin-2(1H)-one
C11H8F3NO3     相似度:50%
Journal of Heterocyclic Chemistry          2008          45          165-172
Fluorescent 6-hydroxy-and 6,7-dihydroxy-4-trifluoro-methylcarbostyrils and formation of o-carboxymethylated derivatives via o-succinimide esters
Georg Uray,Naresh S. Badgujar,Sona Kováčková and Wolfgang Stadlbauer
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

8 .     3-[2-(2-thienyl)-thiazol-4-yl]-(R,S)-2-mercaptopropanoic acid
C10H9NO2S3     相似度:50%
Journal of Heterocyclic Chemistry          2003          40          435-442


Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

9 .     1-[(5-carboxamido)-1,2,3-triazol-4-yl]benzimidazolone
C10H8N6O2     相似度:50%
Journal of Heterocyclic Chemistry          2000          37          1169-1176
1-(1,2,3-triazol-4-yl)-benzimidazolones, a new series of heterocyclic derivatives
Lucia Bertelli, Giuliana Biagi, Vincenzo Calderone, Irene Giorgi, Oreste Livi, Valerio Scartoni and Pier Luigi Barili
Structure      13C NMR   碳谱模拟图
--------------------------------------------------------------------------------

10 .     1-[(5-carboxy)-1,2,3-triazol-4-yl]benzimidazolone
C10H7N5O3     相似度:50%
Journal of Heterocyclic Chemistry          2000          37          1169-1176
1-(1,2,3-triazol-4-yl)-benzimidazolones, a new series of heterocyclic derivatives
Lucia Bertelli, Giuliana Biagi, Vincenzo Calderone, Irene Giorgi, Oreste Livi, Valerio Scartoni and Pier Luigi Barili
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