Поиск подструктуры

CCC1CC(=O)C=CN1C(=O)OCc1ccccc1

CCC1CC(=O)C=CN1C(=O)OCc1ccccc1
Reaction #44012
82
Выход 89.9%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC(=O)CC(c2ccc(Cl)cc2)N1C(=O)OCc1ccccc1
Reaction #44013
83
Выход 33.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC1CC(=O)CC(c2ccc(Cl)cc2)N1C(=O)OCc1ccccc1
Reaction #192420
DOI: 10.1039/C8SC04228D
O=C1C=CN(C(=O)OCc2ccccc2)C(Cc2ccccc2)C1
Reaction #351790
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1CCN[C@H](Cc2ccccc2)C1
Reaction #351791
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1CC(=O)C=CN1C(=O)OCc1ccccc1
Reaction #624553
benzyl 2-allyl-4-oxo-3,4-dihydropyridine-1(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CN(C(=O)OCc2ccccc2)C(C2CCCCC2)C1
Reaction #624915
Benzyl 2-cyclohexyl-4-oxo-3,4-dihydropyridine-1(2H)-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCN(C(=O)OCc2ccccc2)C(C2CCCCC2)C1
Reaction #624916
Benzyl 2-cyclohexyl-4-oxopiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CN(C(=O)OCc2ccccc2)C(Cc2ccccc2)C1
Reaction #1120478
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1CCN[C@H](Cc2ccccc2)C1
Reaction #1120479
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C=CN(C(=O)OCc2ccccc2)C(Cc2ccccc2)C1
Reaction #1824147
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O[C@@H]1CCN[C@H](Cc2ccccc2)C1
Reaction #1824148
title compound
DOI: 10.6084/m9.figshare.5104873.v1