子结构搜索

Cc1ccccc1Br

CC(C)(C)OC(=O)N1CCN(c2ccc(F)cc2C(F)(F)F)CC1
Reaction #181
收率 73.5%
C[C@@H]1CN(c2ccc(F)cc2C(F)(F)F)CCN1
Reaction #595
收率 59.0%
C[C@@H]1CN(c2ccc(F)cc2C(F)(F)F)CCN1
Reaction #596
收率 59.0%
CC(=O)c1cc(Cl)ccc1Nc1cc2c3c(c1)[C@@H]1CNCC[C@@H]1N3CCSC2
Reaction #51562
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Br)ccc2c1C(=Cc1[nH]c3c(c1CCC(=O)O)CCCC3)C(=O)N2
Reaction #52805
3-[2-(5-bromo-4-methyl-2-oxo-1,2-dihydroindol-3-ylidenemethyl)-4,5,6,7-tetrahydro-1H-indol-3-yl]-propionic acid
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cc(F)ccc2Br)OCCO1
Reaction #79340
2-(2-bromo-5-fluorophenyl)-2-methyl-1,3-dioxolane
收率 60.2%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cc(F)ccc2B(O)O)OCCO1
Reaction #79341
4-fluoro-2-(2-methyl-1,3-dioxolan-2-yl)phenylboronic acid
收率 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(N)c1Br
Reaction #79592
methyl 2-bromo-3-aminobenzoate
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(NC2=CC(=O)CC(C)C2)c1Br
Reaction #79593
3-(3-carbomethoxy-2-bromoanilino)-5-methyl-cyclohex-2-en-1-one
收率 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(N)c1Br
Reaction #79611
methyl 2-bromo-3-aminobenzoate
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(NC2=CC(=O)CC(c3ccc(C(F)(F)F)cc3)C2)c1Br
Reaction #79612
3-(3-carbomethoxy-2-bromoanilino)-5-(4-trifluoromethylphenyl)-cyclohex-2-en-1-one
收率 74.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(N)c1Br
Reaction #79626
methyl 2-bromo-3-aminobenzoate
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(N)c1Br
Reaction #79627
methyl 2-bromo-3-aminobenzoate
收率 99.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(NC2=CC(=O)CCC2)c1Br
Reaction #79628
3-(3-carbomethoxy-2-bromoanilino)cyclohex-2-en-1-one
收率 92.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2cc(Cl)ccc2C(F)(F)F)c(Cl)cn1
Reaction #84987
5-Chloro-4-[5-chloro-2-(trifluoromethyl)phenyl]-2-methoxypyridine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1=C(CN2CCOC[C@H]2C(=O)O)NC(c2ncoc2C)=N[C@H]1c1ccc(F)cc1Br
Reaction #91960
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1=C(CN2CCOC[C@H]2C(=O)O)NC(c2ncoc2C)=N[C@H]1c1ccc(F)cc1Br
Reaction #91962
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccn(-c3cccc(C(F)(F)F)c3)n2)cc1Br
Reaction #157433
solid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(=O)c1cc(-c2ccn(-c3cccc(C(F)(F)F)c3)n2)ccc1C
Reaction #157434
oil
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)/C(=C/c1cc(OCc2ccccc2)c(C)cc1Br)NC(=O)OCc1ccccc1
Reaction #160511
title compound
收率 58.1%DOI: 10.6084/m9.figshare.5104873.v1
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