cyclohexylisocyanate
Reaction #3537
title compound
Выход 71.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Reaction #3892
N-cyclohexyl-S-{3-[4-(4-chlorobenzyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride
Выход 100.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Reaction #3931
N-cyclohexyl-S-{3-[4-(4-chlorophenethyl)piperazin-1-yl]propyl}thiocarbamate dihydrochloride
Выход 170.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Reaction #4717
N-Cyclohexyl-N'-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]1,2-hydrazine dicarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
Reaction #9505
N-cyclohexyl-N′-[1,1-dimethyl-2-(3-nitro-7-phenylquinolin-4-ylamino)ethyl]urea
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Reaction #10119
N-{[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]methyl}(cyclohexylamino)carboxamide
Выход 49.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Reaction #57158
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Reaction #60758
4-Amino-3-(3-((cyclohexyl)aminocarbonylamino)phenyl)furo[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Reaction #75756
N-[4-(4-amino-2-butyl-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)butyl]-N′-cyclohexylurea
Выход 66.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
Reaction #91793
1-cyclohexyl-3-[2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-urea
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Reaction #91800
1-cyclohexyl-3-[2-(2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-urea
Выход 52.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Reaction #94254
colorless solid
Выход 39.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
Reaction #94627
6-(7-chloro-1,8-naphthyridin-2-yl)-5-cyclohexylaminocarbonyloxy-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazine
Выход 41.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
Reaction #162961
title compound
Выход 75.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Reaction #173839
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction #175257
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction #175861
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction #176844
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction #177085
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaction #180651
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Страница 1Далее