子结构搜索

ClCc1ccc(Cl)cc1

CN(C)Cc1ccc([C@H]2CC[C@H](OC(=O)c3ccc(Cl)cc3)CC2)cc1
Reaction #1747
trans-O-(4-Chlorobenzoyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)Cc1ccc([C@H]2CC[C@@H](OC(=O)c3ccc(Cl)cc3)CC2)cc1
Reaction #1754
cis-O-(4-Chlorobenzoyl)-4-(4-dimethylaminomethylphenyl)-cyclohexanol
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Cc1ccc(C(Cl)c2ccc(Cl)cc2)cc1
Reaction #2200
desired product
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1)c1ccc(Cl)cc1Cl
Reaction #3587
desired product
收率 53.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)ccc1C(=O)Cl
Reaction #3609
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)ccc1C(=O)Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1
Reaction #3610
desired product
收率 41.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)N2Cc3cccn3Cc3ccccc32)ccc1NC(=O)c1ccc(Cl)cc1Cl
Reaction #3660
crystals
收率 84.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(NC(=O)c2ccc(Cl)cc2Cl)cc1Cl
Reaction #3667
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2n1Cc1ccccc1N(C(=O)c1ccc(NC(=O)c3ccc(Cl)cc3Cl)c(C)c1)C2
Reaction #3695
solid
收率 55.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N2Cc3nccn3Cc3ccccc32)cc1)c1ccc(Cl)cc1Cl
Reaction #3701
tan foam
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N2CCc3cccn3-c3ccccc32)c(Cl)c1)c1ccc(Cl)cc1Cl
Reaction #3705
white solid
收率 99.2%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(Cn2ccc3ccccc32)cc1
Reaction #5689
1-(4-chlorobenzyl)indole
收率 84.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(c1cn(Cc2ccc(Cl)cc2)c2ccccc12)N(C)Cc1cccc(C(F)(F)F)c1
Reaction #5707
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(NCCCSc1ccncc1)c1ccc(Cl)cc1
Reaction #6200
desired compound
收率 118.6%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(-c2ccc(OC)c(F)c2)nn(Cc2ccc(Cl)cc2)c1=O
Reaction #8119
title compound
收率 97.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccc(Cl)cc4)c3C2=O)C(=O)N1
Reaction #10101
4-chloro-N-[2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]-benzamide
收率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCOc1ccc(C(=O)NNC(=O)c2cc(Cl)ccc2Cl)cc1
Reaction #11274
required product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC1CCCC(C(=O)c2ccc(Cl)cc2Cl)C1=O
Reaction #40891
ethyl [3-(2,4-dichlorobenzoyl)-2-oxocyclohexyl]acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccc(Cl)cc3)S(=O)(=O)c3ccc(F)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43824
{5-[(4-Chloro-benzyl)-(4-fluoro-benzenesulfonyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc2cc(N(Cc3ccccc3)C(=O)c3ccc(Cl)cc3)ccc2n1CC(=O)OC(C)(C)C
Reaction #43868
subtitle compound
DOI: 10.6084/m9.figshare.5104873.v1
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