Recherche de Sous-structure

Nc1ccccc1N1CCCCC1

CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1N1CCC[C@@H](N(C)C)C1
Reaction #835
Rendement 7.3%
CC1CCN(c2cc3nc(C(C)(C)C)sc3cc2[N+](=O)[O-])CC1
Reaction #5881
2-tert-butyl-5-(4-methylpiperidin-1-yl)-6-nitrobenzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(c2cc3nc(C(C)(C)C)sc3cc2N)CC1
Reaction #5882
6-amino-2-tert-butyl-5-(4-methylpiperidin-1-yl)benzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(c2cc3nc(C(C)(C)C)sc3cc2N=C=S)CC1
Reaction #5883
2-tert-butyl-6-isothiocyanato-5-(4-methylpiperidin-1-yl)benzothiazole
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN[C@@H]1CCCN2c3cc(Cl)ccc3N(C)c3ccccc3[C@H]12
Reaction #44464
title compound
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1c2ccccc2[C@@H]2[C@H](NCC(=O)O)CCCN2c2cc(Cl)ccc21
Reaction #44465
title compound
Rendement 12.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@@H]1CCCN2c3cc(Cl)ccc3Nc3ccccc3[C@H]12)C(F)(F)F
Reaction #44470
trans-N-(7-Chloro-1,2,3,4,10,14b-hexahydrodibenzo[b,f]pyrido[1,2-d][1,4]diazepin-1-yl)-2,2,2-trifluoroacetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CCN(c2ccccc2[N+](=O)[O-])CC1
Reaction #61157
title compound
Rendement 5.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC1CCN(c2ccccc2N)CC1
Reaction #61158
title compound
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2ccccc2N2CCCCC2)[nH]1
Reaction #61163
title compound
Rendement 45.3%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(Cl)cc1N1CCCCC1
Reaction #61164
title compound
Rendement 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(N2CCCCC2)c1
Reaction #61165
title compound
Rendement 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N)c(N2CCCCC2)c1
Reaction #61166
title compound
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NC(=O)c2ccc(C#N)o2)c(N2CCCCC2)c1
Reaction #61167
title compound
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-n2ccnc2)cc1N1CCCCC1
Reaction #61168
title compound
Rendement 92.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-n2ccnc2)cc1N1CCCCC1
Reaction #61169
title compound
Rendement 66.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2ccc(-n3ccnc3)cc2N2CCCCC2)o1
Reaction #61170
title compound
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #61171
1.10
Rendement 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1ccc([N+](=O)[O-])c(N2CCCCC2)c1
Reaction #61172
title compound
Rendement 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CNc1ccc(NC)c(N2CCCCC2)c1
Reaction #61173
title compound
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant