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CC(N)c1c(F)cccc1F

CC1(C)OC(=O)c2ccc(C(c3c(F)cc([N+](=O)[O-])cc3F)n3cncn3)cc21
Reaction #50336
5-[(2,6-difluoro- 4-nitrophenyl)-[1,2,4]triazol-1-yl-methyl]-3,3-dimethyl-3H-isobenzofuran-1-one
Выход 67.4%DOI: 10.6084/m9.figshare.5104873.v1
CCn1cc(-c2ccnc3[nH]c(-c4ccc(CN5CCOCC5)cc4)cc23)c(-c2ccc(NC(=O)CN(C)C)cc2)n1
Reaction #57170
title product
Выход 57.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)c(C2CCc3cncn32)c(F)c1
Reaction #164062
4-(6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)-3,5-difluorobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn2c3c(c(C4(NC(=O)OCc5ccccc5)CC4)c(F)cc3c1=O)N(C)CC2C
Reaction #234190
DOI: 10.1039/C8SC04228D
CC(=NO)c1cnc2nnn(C(C)c3c(F)cc4ncccc4c3F)c2n1
Reaction #280220
DOI: 10.1039/C8SC04228D
CC(Nc1nc(Br)cnc1N)c1c(F)cc2ncccc2c1F
Reaction #284214
DOI: 10.1039/C8SC04228D
CC(=NOCCO)c1cnc2nnn(C(C)c3c(F)cc4ncccc4c3F)c2n1
Reaction #299497
DOI: 10.1039/C8SC04228D
CC(=O)c1cnc2nnn(C(C)c3c(F)cc4ncccc4c3F)c2n1
Reaction #388019
DOI: 10.1039/C8SC04228D
CC1(C)OC(=O)c2ccc(C(c3c(F)cc([N+](=O)[O-])cc3F)n3cncn3)cc21
Reaction #393429
DOI: 10.1039/C8SC04228D
CC(N=[N+]=[N-])c1c(F)cccc1F
Reaction #501279
1-(2,6-difluorophenyl)ethyl azide
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1c(F)cccc1F)n1cc(C(=O)O)nn1
Reaction #501280
1-(2,6-difluorophenyl)ethyl-1H-1,2,3-triazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(C(C)c2c(F)cccc2F)nn1
Reaction #501281
ethyl 1-[1-(2,6-difluorophenyl)ethyl]-1H-1,2,3-triazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(N=[N+]=[N-])c1c(F)cccc1F
Reaction #501282
2-(2,6-difluorophenyl)-2-azidopropane
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c(C2CNC(=O)N2c2ccc3[nH]cnc3c2)c(F)c1
Reaction #539252
1-(1H-benzo[d]imidazol-5-yl)-5-(2,6-difluoro-4-methoxyphenyl)imidazolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCC(c2c(F)cccc2F)N1c1ccc2[nH]cnc2c1
Reaction #539257
1-(1H-benzo[d]imidazol-5-yl)-5-(2,6-difluorophenyl)imidazolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=CC[C@H](NC(=O)Oc1ccccc1)c1c(F)ccc(Cl)c1F
Reaction #603390
desired product
Выход 100.0%DOI: 10.6084/m9.figshare.5104873.v1
O=CC[C@H](NC(=O)Oc1ccccc1)c1c(F)ccc(Cl)c1F
Reaction #603391
desired product
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
OC[C@H]1CC[C@@H](c2c(F)cc(F)cc2F)N1
Reaction #641155
title compound
Выход 100.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC=C[C@H]2CC[C@@H](c3c(F)cc(F)cc3F)N12
Reaction #641156
title compound
Выход 55.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC[C@@H]2CC[C@@H](c3c(F)cc(F)cc3F)N12
Reaction #641157
title compound
Выход 99.6%DOI: 10.6084/m9.figshare.5104873.v1
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