An 46 Reaktionen beteiligt

1281320

CCCC(CCC)C(=O)OCCC(=O)OC1COC(c2ccccc2)OC1
Reaction #70093
solid
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(Cl)OC1COC(c2ccccc2)OC1
Reaction #70099
2-phenyl-1,3-dioxan-5-yl carbonochloridate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CC1(C)c2cc(OC3COC(c4ccccc4)OC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #89982
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
OC1COC(c2ccccc2)OC1
Reaction #198249
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
c1ccc(COC2COC(c3ccccc3)OC2)cc1
Reaction #232906
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
OC1COC(c2ccccc2)OC1
Reaction #322876
desired title compound
Ausbeute 21.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
c1ccc(COC2COC(c3ccccc3)OC2)cc1
Reaction #322877
desired title compound
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_02
OC1COC(c2ccccc2)OC1
Reaction #373414
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(OC1COC(c2ccccc2)OC1)C12CC3CC(CC(C3)C1)C2
Reaction #633536
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_05
Cc1cc(F)ccc1-c1nc(OC(CO)CO)nc2c1ccc(=O)n2-c1c(F)cccc1F
Reaction #643783
product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
OC1COC(c2ccccc2)OC1
Reaction #682426
2-phenyl-1,3-dioxan-5-ol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COC1COC(c2ccccc2)OC1
Reaction #682427
5-methoxy-2-phenyl-1,3-dioxane
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
COc1ccccc1COC1COC(c2ccccc2)OC1
Reaction #766642
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
c1ccc(C2OCC(OCc3cccs3)CO2)cc1
Reaction #895703
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Clc1ccc2nc(OC3COC(c4ccccc4)OC3)nc(NCc3ccc4c(c3)OCO4)c2c1
Reaction #1034493
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
OC1COC(c2ccccc2)OC1
Reaction #1062801
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_03
Cc1ccc(S(=O)(=O)OC2COC(c3ccccc3)OC2)cc1
Reaction #1098648
white solid
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
Fc1cccc(CSc2nc(Cl)cc(OC3COC(c4ccccc4)OC3)n2)c1F
Reaction #1112015
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_05
Cc1ccc(S(=O)(=O)OC2COC(c3ccccc3)OC2)cc1
Reaction #1200137
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Cc1ccc(S(=O)(=O)OC2COC(c3ccccc3)OC2)cc1
Reaction #1244273
white solid
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_10
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