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1271813

COc1cc(Cl)c(CC2CCN(C3CCC(=O)CC3)C2=O)c(Cl)c1
Reaction #190342
DOI: 10.1039/C8SC04228D
O=C1CCCN1C1CCC2(CC1)OCCO2
Reaction #228081
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC2(CCC1N1CCC(NC(=O)OCc3ccccc3)C1=O)OCCO2
Reaction #264085
DOI: 10.1039/C8SC04228D
CC1CC(=O)CCC1N1CCC(Cc2ccc(Cl)cc2Cl)C1=O
Reaction #378841
DOI: 10.1039/C8SC04228D
CC1CC2(CCC1N1CCC(Cc3ccc(Cl)cc3Cl)C1=O)OCCO2
Reaction #384791
DOI: 10.1039/C8SC04228D
O=C1CCC(N2CCCC2=O)CC1
Reaction #754332
DOI: 10.1039/C8SC04228D
CC1(N2CCCC2=O)CCC2(CC1)OCCO2
Reaction #781691
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC2(CCC1N1CCC(NC(=O)OCc3ccccc3)C1=O)OCCO2
Reaction #909127
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CC(=O)CCC1N1CCC(NC(=O)OCc2ccccc2)C1=O
Reaction #1042292
DOI: 10.1039/C8SC04228D
O=C1CCC(N2C(=O)CCC2=O)CC1
Reaction #1049389
DOI: 10.1039/C8SC04228D
O=C1CCCN1C1CCC2(CC1)OCCO2
Reaction #1100970
title compound
Выход 50.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(CC2CCN(C3CCC4(CC3)OCCO4)C2=O)c(Cl)c1
Reaction #1100971
product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(CC2CCN(C3CCC(=O)CC3)C2=O)c(Cl)c1
Reaction #1100972
3-(2,6-Dichloro-4-methoxy-benzyl)-1-(4-oxo-cyclohexyl)-pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2CC[C@H](NC(=O)OCc3ccccc3)C2=O)CC1
Reaction #1258693
benzyl (3S)-2-oxo-1-(4-oxocyclohexyl)-pyrrolidin-3-ylcarbamate
Выход 100.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(CC2CCN(C3CCC4(CC3)OCCO4)C2=O)c(Cl)c1
Reaction #1294285
DOI: 10.1039/C8SC04228D
CC1(N2CCC(Cc3ccc(Cl)cc3Cl)C2=O)CCC(=O)CC1
Reaction #1306376
DOI: 10.1039/C8SC04228D
CC1CC2(CCC1N1CCCC1=O)OCCO2
Reaction #1320966
DOI: 10.1039/C8SC04228D
O=C1CCC(N2CC[C@H](NC(=O)OCc3ccccc3)C2=O)CC1
Reaction #1461462
benzyl (3S)-2-oxo-1-(4-oxocyclohexyl)-pyrrolidin-3-ylcarbamate
Выход 100.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2CC[C@H](NC(=O)OCc3ccccc3)C2=O)CC1
Reaction #1542559
benzyl (3S)-2-oxo-1-(4-oxocyclohexyl)-pyrrolidin-3-ylcarbamate
Выход 100.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(=O)N1C1CCC2(CC1)OCCO2
Reaction #1635027
DOI: 10.1039/C8SC04228D
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