Participa en 145 reacciones

16148

COC(=O)c1ccc(-c2ncco2)cc1
Reaction #9066
methyl-4-(oxazol-2-yl)-benzoate
Rendimiento 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCN(C)C(=O)c1cc(C(=O)O)cc(-c2ncco2)c1
Reaction #42344
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42350
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1ccc(-c2ncco2)cc1
Reaction #42372
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COC(=O)c1cc(C(=O)O)cc(-c2ncco2)c1
Reaction #42396
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCn1ccc2c(-c3ncco3)cc(C(=O)O)cc21
Reaction #42456
title compound
Rendimiento 70.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN1CCOc2c(-c3ncco3)cc(C(=O)OC)cc21
Reaction #42466
title compound
Rendimiento 71.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCCN(C)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42576
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCCN(CC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42580
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
c1ccc2[nH]ccc2c1.c1cocn1.c1cscn1
Reaction #42621
oxazole thiazole indole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)c1c(C)c(C#N)c(NC(=O)C2CC2)c(O)c1F
Reaction #45619
N-(4-Acetyl-2-cyano-5-fluoro-6-hydroxy-3-methylphenyl)cyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ncco1
Reaction #49226
2-(tributylstannyl)oxazole
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1c(-c2ncco2)nnn1-c1cc(Cl)ccc1NS(=O)(=O)c1ccc(C(C)(C)C)cc1
Reaction #163200
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCCN(CC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #176043
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1OC2(CCN(c3nc4cc(-c5ncco5)ccc4[nH]3)CC2)c2ccccc21
Reaction #185965
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
[Br-]
Reaction #194013
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N1CCC(C(O)c2ncco2)CC1
Reaction #225968
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1ncco1
Reaction #248024
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(N2CCN(C(=O)Cn3nc(-c4ncco4)c4cccnc43)C(C)C2)c(F)cc1Cl
Reaction #251381
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(CCCl)c1ncco1
Reaction #254335
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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