2-(2-(2-methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanol

CC1(OC(=O)COC(=O)CO)C2CC3CC(C2)CC1C3
Reaction #72403
objective compound
Ausbeute 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=C(C)C(=O)OCC(=O)OCC(=O)OC1(C)C2CC3CC(C2)CC1C3
Reaction #72404
compound 3
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=C(C)C(=O)OCC(=O)OCC(=O)OC1(C)C2CC3CC(C2)CC1C3
Reaction #273262
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
CC1(OC(=O)COC(=O)CO)C2CC3CC(C2)CC1C3
Reaction #404976
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1(OC(=O)COC(=O)CO)C2CC3CC(C2)CC1C3
Reaction #973855
2-(2-(2-methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethanol
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
C=C(C)C(=O)OCC(=O)OCC(=O)OC1(C)C2CC3CC(C2)CC1C3
Reaction #973856
2-(2-(2-methyl-2-adamantyloxy)-2-oxoethoxy)-2-oxoethyl methacrylate
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
CC1(OC(=O)COC(=O)CO)C2CC3CC(C2)CC1C3
Reaction #997157
intended compound
Ausbeute 67.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
C=C(C)C(=O)OCC(=O)OCC(=O)OC1(C)C2CC3CC(C2)CC1C3
Reaction #997158
intended compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_09
C=C(C)C(=O)OCC(=O)OCC(=O)OC1(C)C2CC3CC(C2)CC1C3
Reaction #1888617
objective compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01