HgCl2

—
Reaction #6174
liquid
Выход 65.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CCC[Si](C(=O)CC(C)C)(c1ccccc1)c1ccccc1
Reaction #8636
ketone
Выход 88.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=CCC[Si](C)(C(=O)CC(C)C)c1ccccc1
Reaction #8640
ketone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCC(O)CN=C1NC[C@H](c2cccc(F)c2F)CC[C@H]1NC(=O)OC(C)(C)C
Reaction #42672
title compound
Выход 108.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #42676
bis trifluoroacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
S=C=NCCCOc1cccc(CN2CCCCC2)c1
Reaction #63345
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
FC(F)C(F)(F)OC(F)(C(F)(F)F)C(F)(F)F
Reaction #76821
(CF3)2CFOCF2CHF2
Выход 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CC(C)(C)OC(=O)NC1CCC(c2c(F)cccc2F)CNC1=NCC(O)CC(F)(F)F
Reaction #178159
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)N=C(NC(=O)OC(C)(C)C)Nc1cc2ccccc2cn1
Reaction #180173
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1ccc(C(=O)C(C#N)=C(Nc2ccc3oc(C)cc3c2)NC2CCCCN(CC(=O)N3CCCC3)C2=O)cc1
Reaction #197245
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(-c2[nH]c3ncnc(NCC4CCCS4)c3c2-c2ccccc2)cc1
Reaction #206879
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc2c(c1)C1(COCC(N)=N1)c1cc(Br)cc(F)c1O2
Reaction #212350
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C#CCC(O)(C=C)CCCCl
Reaction #213887
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_03
CC(C)(C)OC(=O)N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN/C1=N\CC(O)C1(C(F)(F)F)CC1
Reaction #220314
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CNC(Nc1ccc(OC)c(OC)c1)=C1C(=O)OC(C)(C)OC1=O
Reaction #221226
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C(O)CC1CCc2ccccc21
Reaction #235821
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COC(CNC1=Nc2ccccc2CCC1NC(=O)OCc1ccccc1)OC
Reaction #242017
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
COc1cc(Nc2nc3n(n2)CCCCC3=O)ccc1-n1cnc(Cl)c1
Reaction #261152
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=S(=O)(c1cc2cc(Cl)ccc2[nH]1)N1CCN(C(=NO)c2ncc(-c3ccncc3)cn2)CC1
Reaction #262272
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COc1ccc(CCCCC(=O)O)cc1OC
Reaction #263001
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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