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22394

COC(=O)c1ccc2c(c1)OCc1ccccc1C2OC
Reaction #5140
product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(Br)cc2)c2ccc(Br)cc2)ccc1OCC(=O)O
Reaction #9435
{4-[3,3-bis-(4-bromo-phenyl)-allylsulfanyl]-2-methyl-phenoxy}-acetic acid
Ausbeute 93.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3ccccc3)cc2)c2ccc(-c3ccccc3)cc2)ccc1OCC(=O)O
Reaction #9436
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3ccc(S(C)(=O)=O)cc3)cc2)c2ccc(-c3ccc(S(C)(=O)=O)cc3)cc2)ccc1OCC(=O)O
Reaction #9437
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3cccc(C(F)(F)F)c3)cc2)c2ccc(-c3cccc(C(F)(F)F)c3)cc2)ccc1OCC(=O)O
Reaction #9438
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(SCC=C(c2ccc(-c3ccc(-c4ccccc4)cc3)cc2)c2ccc(-c3ccc(-c4ccccc4)cc3)cc2)ccc1OCC(=O)O
Reaction #9439
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)Nc2cc(Br)ccc2C(=O)c2ccccc2)cc1
Reaction #47162
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(F)cc1)c1ccc(Br)cc1
Reaction #64267
4-bromo-4'-fluorobenzophenone
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCC(c1ccc(Cl)cc1)c1ccc(Br)cc1
Reaction #73768
desired product
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCC(c1ccc(Cl)cc1)c1ccc(-c2cn[nH]c2)cc1
Reaction #73769
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2(c3ccc(Br)cc3)CCNCC2)cc1
Reaction #73775
title compound
Ausbeute 203.1%DOI: 10.6084/m9.figshare.5104873.v1
Clc1ccc(C2(c3ccc(-c4cn[nH]c4)cc3)CCNCC2)cc1
Reaction #73776
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)N1CCC(c2ccc(Cl)cc2)(c2ccc(Br)cc2)CC1
Reaction #73777
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(c2ccc(Cl)cc2)(c2ccc(Br)cc2)CC1
Reaction #73778
desired product
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CNCC(c1ccc(Cl)cc1)c1ccc(Br)cc1
Reaction #73795
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CNCC(c1ccc(Cl)cc1)c1ccc(-c2cn[nH]c2)cc1
Reaction #73796
title compound
Ausbeute 84.2%DOI: 10.6084/m9.figshare.5104873.v1
OC(c1ccc(Cl)cc1)c1ccc(Br)cc1
Reaction #73801
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)N1CCOC(c1ccc(Cl)cc1)c1ccc(Br)cc1
Reaction #73802
title compound
Ausbeute 56.3%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(C2(c3ccc(-c4cn[nH]c4)cc3)CCNCC2)ccc1Cl
Reaction #73837
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(c2ccc(Cl)cc2)(c2ccc(C(=O)O)cc2)CC1
Reaction #73838
4-(4-carboxy-phenyl)-4-(4-chloro-phenyl)-piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
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