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CC(N)=NO

Brc1ccc2c(c1)C1(CCCCC1)C(=NOCc1ccccc1)N2
Reaction #9427
5′-bromospiro{cyclohexane-1,3′-[3H]indol}-2′(1′H)-one 2′(O-benzyloxime)
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)cc1
Reaction #9428
desired product
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)cc1F
Reaction #9429
desired product
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)c1
Reaction #9430
desired product
Ausbeute 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)c1
Reaction #9431
desired compound
Ausbeute 55.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cccc(-c2ccc3c(c2)C2(CCCCC2)C(=NO)N3)c1
Reaction #9432
desired product
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)cc(-c2ccc3c(c2)C2(CCCCC2)C(=NO)N3)c1
Reaction #9433
desired product
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.N/C(=N\O)c1cccc2cc(C(=O)N[C@H]3CN4CCC3CC4)sc12
Reaction #43767
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1c2ncccc2C(=NOC)Nc2c(C)cc(C)nc21
Reaction #81816
title compound
Ausbeute 31.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)N/C(CC1CCC(c2ccc(-c3ccc(Nc4ccc(C(F)(F)F)nc4)nn3)cc2)CC1)=N\O
Reaction #163260
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(CC2CCC(c3ccc(-c4ccc(Nc5ccc(C(F)(F)F)nc5)nn4)cc3)CC2)no1
Reaction #163261
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@@H](NC(=O)N1CC(=NOCC)NC[C@H](Cc2cc(Cl)ccc2OC)C1=O)c1ccc(C(=O)O)c(N)c1.CCC[C@@H](NC(=O)N1CC(=NOCC)NC[C@H](Cc2cc(Cl)ccc2OC)C1=O)c1ccc(C(=O)O)c(N)c1.Cc1ccc(S(=O)(=O)O)cc1.Cc1ccc(S(=O)(=O)O)cc1.Cc1ccc(S(=O)(=O)O)cc1
Reaction #167759
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)Nc1nonc1C(=NO)Nc1cccc(Cl)c1
Reaction #169894
4-[(anilinocarbonyl)amino]-N-(3-chlorophenyl)-N′-hydroxy-1,2,5-oxadiazole-3-carboximidamide
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
ON=C(Nc1ccc(F)c(Br)c1)c1nonc1NCc1nnn[nH]1
Reaction #169917
desired product
Ausbeute 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=N)c1cc(C(=O)NC(C)c2ccc(F)cc2)cc(N(C)S(C)(=O)=O)c1
Reaction #175155
DOI: 10.1039/C8SC04228D
Cc1n[nH]c2cc(Nc3nc(N4CCC(C(N)=NO)CC4)c4occc4n3)ccc12
Reaction #178620
DOI: 10.1039/C8SC04228D
Fc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=NOCc2ccccc2)N3)cc1
Reaction #179743
DOI: 10.1039/C8SC04228D
O=C1c2ccccc2CN2C(=NO)CCC12
Reaction #180492
DOI: 10.1039/C8SC04228D
NC(=NO)c1cccs1
Reaction #180842
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c[nH]nc1NC(C)=NOS(=O)(=O)c1ccc(C)cc1
Reaction #184515
DOI: 10.1039/C8SC04228D
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