Substructure Search

6640

C=CCC1C(=O)c2nc(C3CCCC3c3ccccc3)[nH]c2C(CC=C)C1=O
Reaction #3758
5,7-diallyl-2-(2-phenylcyclopentyl)-1,7-dihydrobenzoimidazole-4,6-dione
Yield 52.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc2nc(-c3ccc(Cl)c(Cl)c3)cc(C(F)(F)F)n2n1
Reaction #11976
5-(3,4-dichloro-phenyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acid
Yield 90.9%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)C2=C(Cl)CCCC2=O)c(Cl)c1
Reaction #62788
3-chloro-2-(2chloro-4-methanesulfonylbenzoyl)cyclohex-2-enone
Yield 70.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCSCc1c(C)cc(C)c(C2CC(=O)C(C(CCC)=NOCC)=C(O)C2)c1C
Reaction #64059
5-[3-(n-Butylthiomethyl)-2,4,6-trimethylphenyl]-2-[1-(ethoxyimino)butyl]-3-hydroxycyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)C1=C(O)CC(c2c(C)cc(O)cc2C)CC1=O
Reaction #64060
5-(2,6-dimethyl-4-hydroxyphenyl)-3-hydroxy-2-propionylcyclohex-2-en-1-one
Yield 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)C1=C(O)CC(c2c(C)cc(OC(C)=O)cc2C)CC1=O
Reaction #64062
5-(4-acetyloxy-2,6-dimethylphenyl)-3-hydroxy-2-propionylcyclohex-2-en-1-one
Yield 42.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1sc(-c2ccc(Cl)cc2)nc1C1=C(OC(=O)C(C)(C)C)C2CCC(C2)C1=O
Reaction #74189
2,2-dimethylpropionic acid 3-[2-(4-chlorophenyl)-5-ethylthiazol-4-yl]-4-oxobicyclo[3.2.1]oct-2-en-2-yl ester
Yield 81.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)C1(CCN1CCC(c2noc3cc(F)ccc23)CC1)c1ccccc1
Reaction #83984
2-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-2-phenyl-1,3-indandione
DOI: 10.6084/m9.figshare.5104873.v1
COC12C=CC(CC1)C(=O)CC2=O
Reaction #159459
1-methoxybicyclo[3.2.2]non-6-en-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
CCc1ccc(-c2ccc(Cl)cc2)cc1C1C(=O)C2C=CC(OC)(CC2)C1=O
Reaction #159460
3-(4′-chloro-4-ethylbiphen-3-yl)-1-methoxybicyclo[3.2.2]non-6-ene-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC(=O)C(F)(F)F)c1ccc(F)cc1
Reaction #170442
title compound
Yield 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)C(C(=O)c2ccc(C(F)F)c3ncccc23)=C(Cl)C(C)(C)C1=O
Reaction #182593
DOI: 10.1039/C8SC04228D
CC1(c2ccc(Cl)cc2)C(=O)c2cc(O)c(Cl)c(Cl)c2C1=O
Reaction #184765
DOI: 10.1039/C8SC04228D
CCC(C)C1CC(=O)C(C(=O)NS(=O)(=O)c2ccc(C)cc2)C(=O)C1
Reaction #185229
DOI: 10.1039/C8SC04228D
Cc1ccc(Cl)c(C2CC(=O)C=C(N)C2)c1
Reaction #187481
DOI: 10.1039/C8SC04228D
CCC(=O)C1=C(O)C(c2ccc(C)c(S(=O)(=O)Cl)c2)CCC1=O
Reaction #190696
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(C(=O)C2=C(Cl)CCCC2=O)c(Cl)c1
Reaction #193264
DOI: 10.1039/C8SC04228D
CC(=O)C(=CNc1ccc(C2=NNC(=O)CC2)cc1)C(C)=O
Reaction #197675
DOI: 10.1039/C8SC04228D
CC(O)C(=N)NS(=O)(=O)c1cc(C(=O)C(C(=O)c2cccc(F)c2)=C2Nc3ccccc3N2)ccc1F
Reaction #212730
DOI: 10.1039/C8SC04228D
O=C(CC(=O)C(F)F)c1ccc(Br)s1
Reaction #216391
needles
Yield 73.3%DOI: 10.6084/m9.figshare.5104873.v1
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