(2,2-dimethyl-1,3-dioxolan-4-yl)methyl 4-methylbenzenesulfonate

CCNC(=O)Nc1ccc(-c2nc3c(c(N4CCOCC4C)n2)CCN(CC2COC(C)(C)O2)C3)cc1
Reaction #192279
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC1(C)OCC(COc2ccc(B3OC(C)(C)C(C)(C)O3)cc2)O1
Reaction #260849
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CC1(C)OCC(Cn2cc(I)cn2)O1
Reaction #298467
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Cc1nn(CC2COC(C)(C)O2)c(C)c1I
Reaction #299988
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cc(OCC(O)CO)ccc1-c1n[nH]c2nc(Oc3ccc(F)cc3F)ncc12
Reaction #317341
3-{4-[6-(2,4-difluoro-phenoxy)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-3-methyl-phenoxy}-propane-1,2-diol
Rendimiento 15.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
Cc1cc(OCC(O)CO)ccc1-c1n[nH]c2nc(Oc3ccc(F)cc3F)ncc12
Reaction #358270
3-{4-[6-(2,4-difluorophenoxy)-1H-pyrazolo[3,4-d]pyrimidin-3-yl]-3-methyl-phenoxy}-propane-1,2-diol
Rendimiento 15.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CC(c1c(OCC2COC(C)(C)O2)ccc(F)c1Cl)c1cn(C(=O)OC(C)(C)C)c2ncc(Br)cc12
Reaction #376690
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1(C)OCC(Cn2cc(I)cn2)O1
Reaction #395267
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC(c1c(OCC2COC(C)(C)O2)ccc(F)c1Cl)c1cn(C(=O)OC(C)(C)C)c2ncc(Br)cc12
Reaction #403874
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1cc(OCC2COC(C)(C)O2)cc(C(=O)NC2CCN(C(=O)OC(C)(C)C)CC2)c1
Reaction #589618
title compound
Rendimiento 71.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CC1(C)OCC(Cn2cc([N+](=O)[O-])cn2)O1
Reaction #609822
1-((2,2-dimethyl-1,3-dioxolan-4-yl)methyl)-4-nitro-1H-pyrazole
Rendimiento 88.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
CC1(C)OCC(CN=[N+]=[N-])O1
Reaction #759533
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COC(=O)c1cc(OCC2COC(C)(C)O2)cc(C(=O)OC)c1
Reaction #778464
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC1(C)OCC(CN2CCN(C(=O)OCc3ccccc3)CC2)O1
Reaction #780011
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
CC1(C)OCC(Cn2cc(B3OC(C)(C)C(C)(C)O3)cn2)O1
Reaction #907878
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cc1ccc(NC(=O)C2(c3ccc4c(c3)OC(F)(F)O4)CC2)nc1-c1cccc(OCC2COC(C)(C)O2)c1
Reaction #924206
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CC1(C)CCn2c1cc1cc([N+](=O)[O-])c(F)cc12
Reaction #924912
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CC1(C)OCC(COc2cccc(Cl)n2)O1
Reaction #973093
title compound
Rendimiento 94.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CC1(C)OCC(CN=[N+]=[N-])O1
Reaction #1098639
13
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CC1(C)OCC(COc2ccc(F)c(C(=O)c3ccc(Nc4ccc(F)cc4F)cc3Cl)c2)O1
Reaction #1099839
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
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