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O=C(Cl)COC1CCCCC1

O=C(Cl)COC1CCCCC1
Reaction #84544
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)COC1CCCCC1
Reaction #84545
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CCC(OC(=O)C(=O)Cl)CC1
Reaction #202241
DOI: 10.1039/C8SC04228D
O=C(Cl)C12CC3CC(CC(C3)O1)C2
Reaction #341842
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C12CC3CC(CC(C3)O1)C2
Reaction #342315
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C1CCC(OC(=O)C(=O)Cl)CC1
Reaction #443878
4-t-butylcyclohexyl chlorooxalate
Ausbeute 95.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C12CC3CC(CC(C3)O1)C2
Reaction #625983
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OCC(=O)Cl)C1
Reaction #889336
DOI: 10.1039/C8SC04228D
CC1CCC(C(C)C)C(OCC(=O)O)C1
Reaction #1197321
L-menthoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OCC(=O)O)C1
Reaction #1197322
L-menthoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OCC(=O)O)C1
Reaction #1197323
L-menthoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OCC(=O)O)C1
Reaction #1197324
L-menthoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OCC(=O)O)C1
Reaction #1197325
L-menthoxyacetic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C12CC3CC(CC(C3)O1)C2
Reaction #1557206
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1738945
N-(L-menthoxyacetyl)-2-pyrroline
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(C(=O)N2CC(F)(F)C2)c(NC(=O)C23CC4CC(CC(C4)O2)C3)c1
Reaction #2285453
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)ccc1NC(=O)C12CC3CC(CC(C3)O1)C2)N1CC(F)(F)C1
Reaction #2285454
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1c(F)cccc1NC(=O)C12CC3CC(CC(C3)O1)C2)N1CC(F)(F)C1
Reaction #2285455
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(C(C)C)C(OCC(=O)Cl)C1
Reaction #2458616
title compound
Ausbeute 107.4%DOI: 10.6084/m9.figshare.5104873.v1