2-bromo-4-fluoro-1-iodo-benzene

COc1ccc(Sc2cc(F)ccc2Br)cc1
Reaction #43481
2-Bromo-5-fluoro-1-(4-methoxy-phenylsulfanyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Sc2ccc(Cl)cc2)c(Br)c1
Reaction #43482
1-Bromo-2-(4-chloro-phenylsulfanyl)-5-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(Sc2ccc(F)cc2Br)c(C)c1
Reaction #43488
1-Bromo-5-fluoro-2-(2,4-dimethyl-phenylsulfanyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Sc2ccc(F)cc2Br)cc1
Reaction #43489
1-Bromo-2-(4-fluoro-phenylsulfanyl)-5-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Sc2ccc(F)cc2Br)c(Cl)c1
Reaction #43490
1-Bromo-2-(2-chloro-4-fluoro-phenylsulfanyl)-5-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(Sc2ccc(F)cc2Br)cc1
Reaction #43491
1-Bromo-5-fluoro-2-(4-methyl-phenylsulfanyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cccc(Sc2ccc(F)cc2Br)c1
Reaction #43492
1-Bromo-5-fluoro-2-(3-methoxy-phenylsulfanyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(Sc2ccc(F)cc2Br)c(Cl)c1
Reaction #43493
1-Bromo-2-(2-chloro-4-methyl-phenylsulfanyl)-5-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Sc2ccccc2Cl)c(Br)c1
Reaction #43497
1-Bromo-2-(2-chloro-phenylsulfanyl)-5-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Sc2ccc(Cl)cc2Cl)c(Br)c1
Reaction #43498
1-Bromo-2-(2,4-dichloro-phenylsulfanyl)-5-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Sc2ccc(F)cc2Br)c(F)c1
Reaction #43499
1-Bromo-2-(2,4-difluoro-phenylsulfanyl)-5-fluoro-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Fc1ccc(Sc2ccccc2)c(Br)c1
Reaction #43501
1-Bromo-5-fluoro-2-(phenylsulfanyl)-benzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc(Sc2ccc(F)cc2Br)c(Cl)c1
Reaction #201064
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1ccc(Sc2ccc(F)cc2Br)cc1
Reaction #201598
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Fc1ccc(Sc2ccc(Cl)cc2)c(Br)c1
Reaction #232894
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Fc1ccc(Sc2ccccc2Cl)c(Br)c1
Reaction #233214
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Fc1ccc(Sc2ccc(F)cc2Br)c(Cl)c1
Reaction #281149
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(Sc2ccc(F)cc2Br)cc1
Reaction #377573
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1ccc(Sc2ccc(F)cc2Br)c(C)c1
Reaction #383772
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1CCCC1c1ccc(F)cc1Br
Reaction #645306
title compound
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
Страница 1Далее