Substructure Search

249756

C/C=C/c1cc(F)c(F)c(F)c1
Reaction #44599
title compound
Yield 84.1%DOI: 10.6084/m9.figshare.5104873.v1
C/C=C/c1cc(F)c(F)c(F)c1
Reaction #44631
title compound
Yield 84.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC=C(c2cnc(C(=O)O)cn2)CC1
Reaction #45138
5-[1-[(2-methylpropan-2-yl)oxycarbonyl]-3,6-dihydro-2H -pyridin-4-yl]pyrazine-2-carboxylic acid
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(/C=C/B1OC(C)(C)C(C)(C)O1)OCC
Reaction #45472
title compound
Yield 53.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(/C=C/C=O)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45473
title compound
Yield 62.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2coc3c(/C=C/C=O)cnc(N)c23)ccc1NC(=O)c1nc2ccccc2n1C
Reaction #45474
title compound
Yield 36.9%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C/C=C/c1cnc(N)c2c(-c3ccc(Oc4ccccc4)cc3)noc12
Reaction #45524
7-[(1E)-3-(diethylamino)prop-1-enyl]-3-(4-phenoxyphenyl)isoxazolo[4,5-c]pyridin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=CCN(C(=O)OC(C)(C)C)CC2)c2oc(C#N)c(Cc3ccccc3)c2c1
Reaction #46467
4-(3-benzyl-2-cyano-5-methyl-benzofuran-7-yl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC/C=C/B1OC(C)(C)C(C)(C)O1
Reaction #52579
product
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccccc1S(=O)(=O)Nc1ccc2[nH]nc(/C=C/c3ccc(Cl)cc3)c2c1
Reaction #53708
N-{3-[(E)-2-(4-chlorophenyl)vinyl]-1H-indazol-5-yl}-2-methylsulfonylbenzenesulfonamide
Yield 65.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC=C(c2cc3c(Br)ccnc3n2S(=O)(=O)c2ccccc2)CC1
Reaction #57201
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cc(C)c(C)cc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #58002
84
DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)C(c2ccc(OC(F)F)cc2)(c2cccc(/C=C/C3CC3)c2)N=C1N
Reaction #58884
title product
Yield 68.5%DOI: 10.6084/m9.figshare.5104873.v1
CCC1(CC)CC=C(c2ccc(OC)cc2[N+](=O)[O-])CC1
Reaction #60419
1-(4,4-Diethylcyclohex-1-enyl)-4-methoxy-2-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
COC1CCN(c2ccc([N+](=O)[O-])c(C3=CC(C)(C)CC(C)(C)C3)c2)CC1
Reaction #60426
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1CCN(c2ccc([N+](=O)[O-])c(C3=CCC4(CCCCC4)CC3)c2)CC1
Reaction #60428
title compound
Yield 111.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc([N+](=O)[O-])c1C1=CC(C)(C)CC(C)(C)C1
Reaction #60467
title compound
Yield 99.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc([N+](=O)[O-])c(C2=CC(C)(C)CC(C)(C)C2)c1
Reaction #60491
title compound
Yield 34.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2=CC(C)(C)CC(C)(C)C2)c([N+](=O)[O-])cc1OC
Reaction #60497
title compound
Yield 85.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C=C(c2cc([N+](=O)[O-])ccc2N2CCN(C(=O)OC(C)(C)C)CC2)CC(C)(C)C1
Reaction #60502
title compound
Yield 14.1%DOI: 10.6084/m9.figshare.5104873.v1
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