子结构搜索

684360

COc1cc(CN(CC(C)C)C(CC(=O)O)c2ccc(Cl)cc2)ccc1OCCN1C(=O)CCC1=O
Reaction #90921
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NC1CCCCC1N1C(=O)c2ccccc2C(C(=O)O)C1c1ccc(Cl)cc1Cl
Reaction #191258
DOI: 10.1039/C8SC04228D
CCOC(=O)CC(N)c1ccc(Cl)cc1
Reaction #195857
DOI: 10.1039/C8SC04228D
CCOC(=O)C1c2ccccc2C(=O)N(C2CCCCC2N(C)S(C)(=O)=O)C1c1ccc(Cl)cc1Cl
Reaction #252618
DOI: 10.1039/C8SC04228D
O=C(OCCCc1ccccc1)C1=C(COCCN2CCCCC2)NC(c2cccs2)=NC1c1ccc(Cl)c(Cl)c1
Reaction #411958
title compound
收率 15.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCCc1ccccc1)C1=C(COCCN2CCCCC2)NC(c2ccco2)=NC1c1ccc(Cl)c(Cl)c1
Reaction #411959
title compound
收率 11.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCCc1ccccc1)C1=C(COCCN2CCCCC2)NC(c2ccncc2)=NC1c1ccc(Cl)c(Cl)c1
Reaction #411960
title compound
收率 3.1%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCOCC1=C(C(=O)OCCCc2ccccc2)C(c2ccc(Cl)c(Cl)c2)N=C(c2ccco2)N1
Reaction #411961
title compound
收率 1.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(CCOCC2=C(C(=O)OCCCc3ccccc3)C(c3ccc(Cl)c(Cl)c3)N=C(c3ccco3)N2)CC1
Reaction #411962
title compound
收率 5.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCCc1ccccc1)C1=C(COCCN2CCCCC2)NC(c2ccccc2)=NC1c1ccc(Cl)c(Cl)c1
Reaction #411963
title compound
收率 2.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCOCC1=C(C(=O)OCCCc2ccccc2)C(c2ccc(Cl)c(Cl)c2)N=C(c2ccco2)N1
Reaction #411965
title compound
收率 11.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCCc1ccccc1)C1=C(COCCN2CCCCC2)NC(c2ccc(Cl)cc2)=NC1c1ccc(Cl)c(Cl)c1
Reaction #411967
title compound
收率 3.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2=NC(c3ccc(Cl)c(Cl)c3)C(C(=O)OCCCc3ccccc3)=C(COCCN3CCCCC3)N2)cc1
Reaction #411968
title compound
收率 0.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C[C@@H](NC(=O)OC(C)(C)C)c1ccc(Cl)cc1
Reaction #510240
(R)-methyl 3-(tert-butoxycarbonylamino)-3-(4-chlorophenyl)propanoate
收率 199.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1c2ccccc2C(=O)N(C2CCCCC2N)C1c1ccc(Cl)cc1Cl
Reaction #537952
ethyl (3RS,4RS)-2-[(1SR,2SR)-2-aminocyclohexyl]-3-(2,4-dichlorophenyl)-1-oxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1c2ccccc2C(=O)N(C2CCCCC2NS(C)(=O)=O)C1c1ccc(Cl)cc1Cl
Reaction #537953
ethyl(3RS,4RS)-3-(2,4-dichlorophenyl)-2-{(1SR,2SR)-2-[(methylsulfonyl)amino]cyclohexyl}-1-oxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1c2ccccc2C(=O)N(C2CCCCC2N(C)S(C)(=O)=O)C1c1ccc(Cl)cc1Cl
Reaction #537954
ethyl (3RS,4RS)-3-(2,4-dichlorophenyl)-2-{(1SR,2SR)-2-[methyl(methylsulfonyl)amino]cyclohexyl}-1-oxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)NC1CCCCC1N1C(=O)c2ccccc2C(C(=O)O)C1c1ccc(Cl)cc1Cl
Reaction #537955
(3RS,4RS)-3-(2,4-dichlorophenyl)-2-{(1SR,2SR)-2-[(methylsulfonyl)amino]cyclohexyl}-1-oxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylic acid
收率 100.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C2CC=CC=C2C(=O)N(C2CCCCC2N2CCCS2(=O)=O)C1c1ccc(Cl)cc1Cl
Reaction #537959
ethyl(3RS,4RS)-3-(2,4-dichlorophenyl)-2-[(1SR,2SR)-2-(1,1-dioxidoisothiazolidin-2-yl)cyclohexyl]-1-oxo-tetrahydroisoquinoline-4-carboxylate
收率 30.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(CN2CCOCC2C(=O)O)NC(c2nccs2)=NC1c1ccc(Cl)cc1Cl
Reaction #611748
title compound
收率 43.1%DOI: 10.6084/m9.figshare.5104873.v1
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