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644831

CCOC(=O)C1CC(=O)C1
Reaction #202539
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC(O)C1
Reaction #234362
DOI: 10.1039/C8SC04228D
O=C1CC(C(=O)OCc2ccccc2)C1
Reaction #275655
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)C1(C(=O)OC(C)C)CC(=O)C1
Reaction #379668
DOI: 10.1039/C8SC04228D
CC(C)OC(=O)C1(C(=O)OC(C)C)CC(=CC#N)C1
Reaction #381795
DOI: 10.1039/C8SC04228D
CCN(CC)C1CC(C(=O)OCc2ccccc2)C1
Reaction #385134
DOI: 10.1039/C8SC04228D
CCCOC(=O)C1CC(=O)C1
Reaction #387141
DOI: 10.1039/C8SC04228D
COc1ccc(COC(=O)C2CC(=O)C2)cc1
Reaction #562249
4-methoxybenzyl 3-oxocyclobutanecarboxylate
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)C1CC(=O)C1
Reaction #606820
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)C1CC(Nc2nnc[nH]2)C1
Reaction #606821
title compound
Ausbeute 49.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(Nc2nnc(C)[nH]2)C1
Reaction #606963
title compound
Ausbeute 81.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)OC(=O)C1(C(=O)OC(C)C)CC(=O)C1
Reaction #627156
dipropan-2-yl 3-oxocyclobutane-1,1-dicarboxylate
Ausbeute 72.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CC(=O)C1
Reaction #662207
tert-butyl 3-oxocyclobutane-1-carboxylate
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)C1CC(O)(c2ccc(Br)c(F)c2)C1
Reaction #662209
tert-butyl 3-(4-bromo-3-fluorophenyl)-3-hydroxycyclobutane-1-carboxylate
Ausbeute 93.5%DOI: 10.6084/m9.figshare.5104873.v1
C#CC1(O)CC(C(=O)OCC)C1
Reaction #662233
(±)-Ethyl 3-ethynyl-3-hydroxycyclobutane-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(C(=O)OCc2ccccc2)C1
Reaction #802310
title compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(O)CC(C(=O)OCc2ccccc2)C1
Reaction #802311
title compound
Ausbeute 47.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCOC(=O)C1CC(Nc2nnc[nH]2)C1
Reaction #895741
DOI: 10.1039/C8SC04228D
O=C1CC(C(=O)OCc2ccccc2)C1
Reaction #990032
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(O)(c2ccc(F)cc2)C1
Reaction #1007949
Intermediate 276A
Ausbeute 51.0%DOI: 10.6084/m9.figshare.5104873.v1
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