Substructure Search

13037

Fc1ccc(Br)cc1CBr
Reaction #2876
title compound
Yield 96.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1ccc(C2(Br)C=CC=CC2)c(F)c1F
Reaction #7430
formula 13
DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(-c2ccco2)c2cnn(Cc3ccccc3F)c2n1
Reaction #8388
title compound
Yield 80.8%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1Cn1ccc2c(-c3ccco3)nc(Cl)nc21
Reaction #11848
title compound
Yield 76.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccc([N+](=O)[O-])cc2)sc2c1c(=O)n(-c1ccccc1)c(=O)n2Cc1c(F)cccc1F
Reaction #51531
1-(2,6-difluorobenzyl)-5-methyl-6-(4-nitrophenyl)-3-phenylthieno[2,3-d]pyrimidine-2,4(1H, 3H)-dione
Yield 88.1%DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(I)cc1F
Reaction #52339
title compound
Yield 96.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCSCc1ccc(OCc2ccccc2F)cc1
Reaction #53280
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#CCc1ccc(OCc2c(F)cccc2F)cc1
Reaction #53295
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(Oc2ccc(Cl)cc2)C1C(=O)OCc1cc(Oc2ccccc2)ccc1F
Reaction #56377
2-fluoro-5-phenoxybenzyl 3-(4-chlorophenoxy)-2,2-dimethylcyclopropanecarboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)n(Cc2c(F)cccc2C(F)(F)F)cc1Br
Reaction #56781
5-bromo-1-[2-fluoro-6-(trifluoromethyl)benzyl]pyrimidine-2,4(1H,3H)-dione
Yield 68.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2cn(CC3(F)CC=CC=C3C(F)(F)F)c(=O)[nH]c2=O)c1Cl
Reaction #56789
5-(2-chloro-3-methoxyphenyl)-1-[1-fluoro-6-(trifluoromethyl)benzyl]pyrimidine-2,4(1H,3H)-dione
Yield 88.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NS(=O)(=O)c1ccccc1-c1ccc(CBr)c(F)c1
Reaction #64576
title compound
Yield 81.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nn(-c2cc([N+](=O)[O-])ccc2Br)c(=O)n1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)(C)C)cc1F
Reaction #64577
title compound
Yield 93.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)N2Cc3c(F)ccc(F)c3C2)cc1
Reaction #69671
4,7-difluoro-2-(toluene-4-sulfonyl)isoindoline
Yield 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)c3cccc(N4C[C@@H](C)N(Cc5ccccc5)[C@@H](C)C4)c3C2=O)cc1OC
Reaction #70601
Compound 42
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCCN1Cc1ccc([N+](=O)[O-])cc1F
Reaction #72581
title product
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N2CCOCC2)cc2c1nc(C)n2Cc1cccc(C)c1F
Reaction #72783
desired product
Yield 48.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(F)c(CN(Cc2cc(F)c(F)cc2F)c2ccc3[nH]cnc3c2)cc1F
Reaction #74215
N,N-Bis(2,4,5-trifluorobenzyl)-1H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccccc1CN(Cc1ccccc1F)c1ccc2[nH]cnc2c1
Reaction #74225
N,N-Bis(2-fluorobenzyl)-1H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(CN(Cc2cccc(C)c2F)c2ccc3[nH]cnc3c2)c1F
Reaction #74227
N,N-Bis(2-fluoro-3-methylbenzyl)-1H-benzo[d]imidazol-5-amine
DOI: 10.6084/m9.figshare.5104873.v1
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