(4-cyclohexyloxyphenyl)boronic acid

Nc1nccnc1-c1ccc(OC2CCCCC2)cc1
Reaction #174579
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ncc(Cl)cc1-c1ccc(OC2CCCCC2)cc1
Reaction #381713
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Nc1nccnc1-c1ccc(OC2CCCCC2)cc1
Reaction #1492894
3-[4-(cyclohexyloxy)phenyl]pyrazin-2-amine
Выход 77.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Nc1ncc(Cl)cc1-c1ccc(OC2CCCCC2)cc1
Reaction #1492900
title compound
Выход 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Nc1ncc(F)cc1-c1ccc(OC2CCCCC2)cc1
Reaction #1492927
title compound
Выход 81.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Nc1ncccc1-c1ccc(OC2CCCCC2)cc1
Reaction #1493014
title compound
Выход 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Cc1cnc(N)c(-c2ccc(OC3CCCCC3)cc2)n1
Reaction #1493022
title compound
Выход 99.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
Cc1cnc(N)c(-c2ccc(OC3CCCCC3)cc2)n1
Reaction #1493030
title compound
Выход 52.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
C=CC(=O)N1CCC(CNc2ncnc(N)c2-c2ccc(OC3CCCCC3)cc2)CC1
Reaction #1609371
1-(4-(((6-amino-5-(4-(cyclohexyloxy)phenyl)pyrimidin-4-yl)amino)methyl)piperidin-1-yl)prop-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_07
Nc1nccnc1-c1ccc(OC2CCCCC2)cc1
Reaction #1709828
3-[4-(cyclohexyloxy)phenyl]pyrazin-2-amine
Выход 77.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Nc1ncc(Cl)cc1-c1ccc(OC2CCCCC2)cc1
Reaction #1709834
title compound
Выход 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Nc1ncc(F)cc1-c1ccc(OC2CCCCC2)cc1
Reaction #1709860
title compound
Выход 81.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Nc1ncccc1-c1ccc(OC2CCCCC2)cc1
Reaction #1709948
title compound
Выход 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Cc1cnc(N)c(-c2ccc(OC3CCCCC3)cc2)n1
Reaction #1709955
title compound
Выход 99.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Cc1cnc(N)c(-c2ccc(OC3CCCCC3)cc2)n1
Reaction #1709963
title compound
Выход 52.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_07
Nc1nccnc1-c1ccc(OC2CCCCC2)cc1
Reaction #1835094
3-[4-(cyclohexyloxy)phenyl]pyrazin-2-amine
Выход 77.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
Nc1ncc(Cl)cc1-c1ccc(OC2CCCCC2)cc1
Reaction #1835100
title compound
Выход 48.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
Nc1ncc(F)cc1-c1ccc(OC2CCCCC2)cc1
Reaction #1835127
title compound
Выход 81.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
Nc1ncccc1-c1ccc(OC2CCCCC2)cc1
Reaction #1835214
title compound
Выход 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
Cc1cnc(N)c(-c2ccc(OC3CCCCC3)cc2)n1
Reaction #1835222
title compound
Выход 99.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_10
Страница 1Далее