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68388

Cc1ccc(-c2cn3cc([N+](=O)[O-])ccc3n2)cc1
Reaction #63795
yellow solid
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc([N+](=O)[O-])cc3)cn2c1
Reaction #63798
6-Methyl-2-(4-nitrophenyl)imidazo[1,2-a]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)c1c(-c2ccc(C)cc2)nc2ccc(C)cn12
Reaction #255071
DOI: 10.1039/C8SC04228D
Cc1ccc2nc(-c3ccc([N+](=O)[O-])cc3)cn2c1
Reaction #426736
title compound
Ausbeute 40.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(N)cc3)cn2c1
Reaction #426737
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2cn3cc(F)ccc3n2)cc1
Reaction #426738
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2cn3cc(I)ccc3n2)cc1
Reaction #426739
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(NC(=O)c4ccc([N+](=O)[O-])cc4)cc3)cn2c1
Reaction #426744
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(NC(=O)c4ccc(N)cc4)cc3)cn2c1
Reaction #426745
title compound
Ausbeute 78.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(/C=C/c4ccc([N+](=O)[O-])cc4OCCO[Si](C)(C)C(C)(C)C)cc3)cn2c1
Reaction #426777
title compound
Ausbeute 64.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(/C=C/c4ccc([N+](=O)[O-])cc4)cc3)cn2c1
Reaction #426778
title compound
Ausbeute 24.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc([N+](=O)[O-])ccc1/C=C/c1ccc(-c2cn3cc(C)ccc3n2)cc1
Reaction #426779
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(/C=C/c4ccc([N+](=O)[O-])cc4OCCF)cc3)cn2c1
Reaction #426780
title compound
Ausbeute 74.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(/C=C/c4ccc(N)cc4OCCF)cc3)cn2c1
Reaction #426781
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cn3cc(C)ccc3n2)cc1
Reaction #509276
6-methyl-2-p-tolyl-imidazo[1,2-a]pyridine
Ausbeute 70.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cn3cc(C)ccc3n2)cc1
Reaction #542198
white solid
Ausbeute 66.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2cn3cc(C)ccc3n2)cc1
Reaction #587932
6-methyl-2-p-tolyl-imidazo[1,2-a]pyridine
Ausbeute 70.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2nc(-c3ccc(C=O)cc3)cn2c1
Reaction #901113
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2nc3ccc(C)cn3c2CC(=O)N(C)C)cc1
Reaction #925097
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc2nc(-c3ccc(O)cc3)cn2c1
Reaction #997826
2-(4′-hydroxyphenyl)-6-nitroimidazo[1,2-a]pyridine
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1
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