Substructure Search

CCN

CCCCc1nccn1Cc1c(F)cccc1Cl
Reaction #6579
2-n-butyl-1-(2-chloro-6-fluorophenyl)methyl-1H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC(Cc1ccc(O)cc1)C(=O)NC(Cc1ccc(F)cc1)C(=O)N1CC(Cc2ccc3ccccc3c2)NC(=O)C1Cc1c[nH]cn1
Reaction #8632
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)Nc1ccc(-c2nc(-c3ccc(NC(=O)Nc4cccc(C(N)=O)c4)cc3)nc(N3C(C)COCC3C)n2)cc1
Reaction #184870
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCN(C(=O)C5CC5)CC4)[nH]c3cc2Br)CC1
Reaction #188624
DOI: 10.1039/C8SC04228D
CC(=O)N1CCN(C(=O)c2cc3cc(OC4CCN(C(C)C)CC4)ccc3n2C(C)C)CC1
Reaction #190962
DOI: 10.1039/C8SC04228D
CN(CCO)C(=O)CC1CCN(C(=O)C2NC(CC(C)(C)C)C(C#N)(c3ccc(Cl)cc3F)C2c2cccc(Cl)c2F)CC1
Reaction #192114
DOI: 10.1039/C8SC04228D
CCOCCn1c(NC2CCN(CCC3(c4ccc(Cl)c(Cl)c4)CCCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #196540
DOI: 10.1039/C8SC04228D
CCN(CC)C(=O)N1CCN(C(=O)c2cc3cc(OC4CCN(C(C)C)CC4)ccc3[nH]2)CC1
Reaction #199979
DOI: 10.1039/C8SC04228D
CCOC(=O)Cn1cccc1C=C1CN(C(c2ccccc2)(c2ccccc2)c2ccccc2)CCC1=O
Reaction #205333
DOI: 10.1039/C8SC04228D
COC(=O)NCC1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #205365
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(Oc2ccc3c(c2)cc(C(=O)N2CCS(=O)(=O)CC2)n3C(C)C)CC1
Reaction #207138
DOI: 10.1039/C8SC04228D
Cc1cc(C(O)C(C)N2CCC(O)(c3ccc(F)cc3)CC2)ccc1O[Si](C(C)C)(C(C)C)C(C)C
Reaction #208328
DOI: 10.1039/C8SC04228D
Nc1cc(Cl)c(C(F)(F)F)cc1NC(=O)CCC1CC(=O)C1
Reaction #210048
DOI: 10.1039/C8SC04228D
CN1CC(c2ccc(F)cc2)C2(CCCN(C(=O)C(COCc3ccccc3)NC(=O)C(C)(C)NC(=O)OC(C)(C)C)C2)C1=O
Reaction #213709
DOI: 10.1039/C8SC04228D
C[C@@H](n1cnn(-c2ccc(OCC(F)(F)F)cc2)c1=O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216334
4-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-2-[4-(2,2,2-trifluoroethoxy)phenyl]-3(2H,4H)-1,2,4-triazolone
Yield 48.4%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](n1nnn(-c2ccc(OCC(F)(F)F)cc2)c1=O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216352
1-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-4-[4-(2,2,2-trifluoroethoxy)phenyl]-5(1H,4H)-tetrazolone
Yield 41.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)NC1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #223437
DOI: 10.1039/C8SC04228D
CC(C)(C)CC1CN(C(=O)Nc2ccc(C#N)cc2)C(c2cccc(Cl)c2F)C1(C#N)c1ccc(Cl)cc1F
Reaction #227038
DOI: 10.1039/C8SC04228D
CCOCC(=O)N1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #236950
DOI: 10.1039/C8SC04228D
Cc1ccn(-c2ccc(C(=O)N3Cc4cccnc4Oc4ccccc43)c(F)c2)n1
Reaction #242291
DOI: 10.1039/C8SC04228D
Page 1Next