17 件の反応に参加

1162016

COC(=O)C(CCSC)NC(=O)c1ccc(CNC2c3ccccc3-c3ccccc32)cc1-c1ccccc1C
Reaction #187149
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
OC(CCl)CNC1c2ccccc2-c2ccccc21
Reaction #274844
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CCOC(=O)CCNC1c2ccccc2-c2ccccc21
Reaction #778482
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
Fc1cnc(Cl)nc1NC1c2ccccc2-c2ccccc21
Reaction #1232208
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
CN(C)C1(c2ccccc2)CCC(NC2c3ccccc3-c3ccccc32)CC1
Reaction #1266237
N′-(9H-fluoren-9-yl)-N,N-dimethyl-1-phenyl-cyclohexane-1,4-diamine
収率 57.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
CN(C)C1(c2cccs2)CCC(NC2c3ccccc3-c3ccccc32)CC1.Cl.Cl
Reaction #1266246
cis/trans mixture
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_10
COc1cc(C#CC(=O)NC2c3ccccc3-c3ccccc32)ccc1-n1cnc(C)c1
Reaction #1291781
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
Cl.c1ccc2c(c1)COC21CCN(CCNC2c3ccccc3-c3ccccc32)CC1
Reaction #1363808
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_12
COc1cc(C#CC(=O)NC2c3ccccc3-c3ccccc32)ccc1-n1cnc(C)c1
Reaction #1449798
title compound
収率 37.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
COc1cc(C#CC(=O)NC2c3ccccc3-c3ccccc32)ccc1-n1cnc(C)c1
Reaction #1533653
title compound
収率 37.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_02
CC1=C(C(=O)OC2c3ccccc3-c3ccccc32)N2C(=O)[C@@H](NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #1744576
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1976_06
CCOC(=O)CCNC1c2ccccc2-c2ccccc21
Reaction #1816433
N-(9-fluorenyl)-β-alanine ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1994_07
COc1cc(C(=O)NC2c3ccccc3-c3ccccc32)c([N+](=O)[O-])cc1OCc1ccccc1
Reaction #1964007
( 7e )
収率 80.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_11
CN(C)C1(c2ccccc2)CCC(NC2c3ccccc3-c3ccccc32)CC1
Reaction #2247199
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (4/10)
COc1cc(C#CC(=O)NC2c3ccccc3-c3ccccc32)ccc1-n1cnc(C)c1
Reaction #2334662
title compound
収率 37.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_03
COc1cc(C=CC(=O)NC2c3ccccc3-c3ccccc32)ccc1-n1ccnc1
Reaction #2420731
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (10/10)
OC(CCl)CNC1c2ccccc2-c2ccccc21
Reaction #2507703
1-(9-fluorenylamino)-2-hydroxy-3-chloropropane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_08