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O=[N+]([O-])c1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #555560
5-nitro-2-(pyridin-2-yl)-1H-indole
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #555561
2-(pyridin-2-yl)-1H-indol-5-amine
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(C3CCCCN3)cc2c1
Reaction #555566
2-(piperidin-2-yl)-1H-indol-5-amine
Ausbeute 110.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #590555
5-nitro-2-(pyridin-2-yl)-1H-indole
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #590556
2-(pyridin-2-yl)-1H-indol-5-amine
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(C3CCCCN3)cc2c1
Reaction #590561
2-(piperidin-2-yl)-1H-indol-5-amine
Ausbeute 110.6%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc2[nH]c(-c3c[nH]cn3)cc2c1
Reaction #1111029
2-(1H-imidazol-4-yl)-1H-indole
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #1491132
5-nitro-2-(pyridin-2-yl)-1H-indole
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #1491133
2-(pyridin-2-yl)-1H-indol-5-amine
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(C3CCCCN3)cc2c1
Reaction #1491138
2-(piperidin-2-yl)-1H-indol-5-amine
Ausbeute 110.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #1652028
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #1934628
5-nitro-2-(pyridin-2-yl)-1H-indole
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #1934629
2-(pyridin-2-yl)-1H-indol-5-amine
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(C3CCCCN3)cc2c1
Reaction #1934634
2-(piperidin-2-yl)-1H-indol-5-amine
Ausbeute 110.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #1934959
5-nitro-2-(pyridin-2-yl)-1H-indole
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #1934960
2-(pyridin-2-yl)-1H-indol-5-amine
Ausbeute 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2[nH]c(C3CCCCN3)cc2c1
Reaction #1934965
2-(piperidin-2-yl)-1H-indol-5-amine
Ausbeute 110.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc2cc(-c3ccccn3)[nH]c12
Reaction #1938530
title compound
Ausbeute 85.1%DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(Nc1cccc2cc(-c3ccccn3)[nH]c12)c1cccs1
Reaction #1938613
title compound
Ausbeute 84.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2[nH]c(-c3ccccn3)cc2c1
Reaction #1995645
5-nitro-2-(pyridin-2-yl)-1H-indole
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
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