Recherche de Sous-structure

CCOCC(=O)OCCl

CCCO[C@@H]1[C@@H](Cc2ccc(C(F)(F)F)cc2)COC[C@H](NC(=O)c2nccc(OC)c2OCOC(=O)COCC)C(=O)O[C@H]1C
Reaction #87243
((4-methoxy-2-(((3S,7S,8R,9S)-9-methyl-2-oxo-8-propoxy-7-(4-(trifluoromethyl)benzyl)-1,5-dioxonan-3-yl)carbamoyl)pyridin-3-yl)oxy)methyl 2-ethoxyacetate
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COCC(=O)OC(Cl)Cl
Reaction #284461
DOI: 10.1039/C8SC04228D
CCOC(=O)COCC(=O)OC(Cl)Cl
Reaction #413961
ethyl dichloromethyl diglycolate
Rendement 10.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OCc1ccccc1)C(=O)O[C@H](C(=O)OCCl)C(C)C
Reaction #576189
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OCc1ccccc1)C(=O)O[C@H](C(=O)OCI)C(C)C
Reaction #576190
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCCOCC(=O)OCCl
Reaction #773985
DOI: 10.1039/C8SC04228D
CCCO[C@@H]1[C@@H](Cc2ccc(C(F)(F)F)cc2)COC[C@H](NC(=O)c2nccc(OC)c2OCOC(=O)COCC)C(=O)O[C@H]1C
Reaction #796180
((4-methoxy-2-(((3S,7S,8R,9S)-9-methyl-2-oxo-8-propoxy-7-(4-(trifluoromethyl)benzyl)-1,5-dioxonan-3-yl)carbamoyl)pyridin-3-yl)oxy)methyl 2-ethoxyacetate
Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OCc1ccccc1)C(=O)O[C@H](C(=O)OCCl)C(C)C
Reaction #1077119
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OCc1ccccc1)C(=O)O[C@H](C(=O)OCI)C(C)C
Reaction #1077120
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCCOCC(=O)OCCl
Reaction #1147965
Chloromethyl 2-(2-(2-methoxyethoxy)-ethoxy)-ethoxy-acetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OCc1ccccc1)C(=O)O[C@H](C(=O)OCCl)C(C)C
Reaction #1257775
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OCc1ccccc1)C(=O)O[C@H](C(=O)OCI)C(C)C
Reaction #1257776
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C(NC(=O)OCc1ccccc1)C(=O)OC(C(=O)OCCl)C(C)C
Reaction #1307316
DOI: 10.1039/C8SC04228D
CCOC(C)(C)C(=O)OCI
Reaction #1310240
DOI: 10.1039/C8SC04228D
CC(C)C(NC(=O)OCc1ccccc1)C(=O)OC(C(=O)OCI)C(C)C
Reaction #1637446
DOI: 10.1039/C8SC04228D
CCOCC(=O)OCOc1c(OC)ccnc1C(=O)N[C@H]1COC[C@H](OCC(C)C)[C@@H](Oc2cccc(Cl)c2)[C@H](C)OC1=O
Reaction #1714238
title compound
Rendement 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCC[C@H]1[C@H](C)OC(=O)[C@@H](NC(=O)c2nccc(OC)c2OCOC(=O)COCC)CCC[C@@H]1OC(=O)C(C)C
Reaction #1857565
title compound
Rendement 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCC(=O)OCOc1c(OC)ccnc1C(=O)N[C@H]1CCC[C@H](Cc2ccc(C)cc2)[C@@H](OCCCC(F)(F)F)[C@H](C)OC1=O
Reaction #1863303
title compound
Rendement 55.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOCC(=O)OCCl
Reaction #1863305
oil
Rendement 97.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[C@H](NC(=O)OCc1ccccc1)C(=O)O[C@H](C(=O)OCCl)C(C)C
Reaction #1877941
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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