#6803943

O=C(O)c1ccc(I)nc1
Reaction #1320
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1nnn(-c2ccc(O)cc2O)c1-c1ccc(F)cc1
Reaction #40718
1-(2,4-Dihydroxy-phenyl)-5-(4-fluoro-phenyl)-1H-[1,2,3]triazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC1(N)CCN(c2ncc3ncnc(Nc4ccc(F)c(Cl)c4)c3n2)CC1
Reaction #51441
6-(4-amino-4-methylpiperidin-1-yl)-4-(3-chloro-4-fluorophenylamino)-pyrimido[5,4-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
CC(CC(=O)O)c1ccc(-c2ccc(F)cc2F)cc1
Reaction #55180
3-(2',4'-difluoro-4-biphenylyl)butyric acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
CC(CO)n1cnc2c(I)ncnc21
Reaction #55721
9-(1-HYDROXYL-2-PROPYL)-6-IODOPURINE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC(CO)n1cnc2c(I)ncnc21
Reaction #55861
9-(1-HYDROXYL-2-PROPYL)-6-IODOPURINE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
CC(CO)n1cnc2c(I)ncnc21
Reaction #55866
9-(1-HYDROXY-2-PROPYL)-6-IODOPURINE
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
Nc1ncnc(I)c1N
Reaction #60880
title compound
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC1(C)c2ccccc2-c2cc3cc4ccccc4cc3cc21
Reaction #68691
13,13-dimethyl-13H-indeno[1,2-b]anthracene
Ausbeute 58.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(O)c1ccc(I)nc1
Reaction #81593
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=C(O)c1ccc(I)nc1
Reaction #81657
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Clc1cc(N2CC3CCC(C2)O3)nc(I)n1
Reaction #162595
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
Clc1cc(N2C3CCC2COC3)nc(I)n1
Reaction #162613
title compound
Ausbeute 38.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCC1C(=O)Oc2c(Oc3ccccc3Cl)cccc21
Reaction #173572
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCc1ccc(C(=O)C(C)NC(=O)OC(C)(C)C)cc1
Reaction #173744
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1nc(C)sc1I
Reaction #173845
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(-c2ccc3c(N4CCOCC4)nc(Cl)nc3c2)o1
Reaction #174264
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #174641
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Clc1nccc2occc12
Reaction #175133
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1cc(C(=O)N(C)CC(CCN2CCC(C(=O)c3nc4ccccc4[nH]3)CC2)c2ccc(Cl)cc2)cc(OC)c1OC
Reaction #175359
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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