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62953

Cc1c(Cc2ccccc2)c(=O)oc2cc(OC(=O)N3CCCc4ccccc43)ccc12
Reaction #184067
DOI: 10.1039/C8SC04228D
CN(C)C(=O)Oc1ccc2c(CBr)c(Cc3cccc([N+](=O)[O-])c3F)c(=O)oc2c1
Reaction #184301
DOI: 10.1039/C8SC04228D
CC(=O)Cc1c(Cc2cccc([N+](=O)[O-])c2)c(=O)oc2cc(OC(=O)N(C)C)c(Cl)cc12
Reaction #206789
DOI: 10.1039/C8SC04228D
Cc1c(Cc2c(F)cccc2Cl)c(=O)oc2cc(OC(=O)N3CCCc4ccccc43)ccc12
Reaction #221257
DOI: 10.1039/C8SC04228D
Cc1c(Cc2c(Cl)cccc2Cl)c(=O)oc2cc(OC(=O)N(C)c3ccccc3)c(Cl)cc12
Reaction #225983
DOI: 10.1039/C8SC04228D
CN(C)C(=O)Oc1cc2oc(=O)c(Cc3cccc(NS(C)(=O)=O)c3)c(CC(N)=O)c2cc1Cl
Reaction #235458
DOI: 10.1039/C8SC04228D
COC(=O)Cc1c(Cc2cccc([N+](=O)[O-])c2)c(=O)oc2cc(OC(=O)N(C)C)ccc12
Reaction #244318
DOI: 10.1039/C8SC04228D
Cc1c(Cc2ccc(Cl)c(Cl)c2)c(=O)oc2cc(OC(=O)N3CCCc4ccccc43)ccc12
Reaction #251796
DOI: 10.1039/C8SC04228D
Cc1c(Cc2ccc(F)cc2)c(=O)oc2cc(OC(=O)N(C)c3ccccc3)ccc12
Reaction #298754
DOI: 10.1039/C8SC04228D
O=Cc1cccc2ccc(=O)oc12
Reaction #340900
8-formyl coumarin
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cc2c(Cl)cccc2Cl)c(=O)oc2cc(OC(=O)N3CCCc4ccccc43)ccc12
Reaction #371364
DOI: 10.1039/C8SC04228D
Cc1c(Cc2cccc([N+](=O)[O-])c2F)c(=O)oc2cc(O)ccc12
Reaction #687006
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Oc1ccc2c(CF)c(Cc3cccc(N)c3F)c(=O)oc2c1
Reaction #687014
title compound
Ausbeute 102.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Oc1ccc2c(CF)c(Cc3cccc(NS(N)(=O)=O)c3F)c(=O)oc2c1
Reaction #687015
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Oc1cc2oc(=O)c(Cc3cccc(NS(=O)(=O)NC(=O)OC(C)(C)C)c3)c(CF)c2cc1Cl
Reaction #687016
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Oc1cc2oc(=O)c(Cc3cccc(NS(N)(=O)=O)c3)c(CF)c2cc1Cl
Reaction #687017
title compound
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Oc1cc2oc(=O)c(Cc3cccc(NS(C)(=O)=O)c3)c(CC(N)=O)c2cc1Cl
Reaction #687018
title compound
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Oc1ccc2c(CBr)c(Cc3cccc([N+](=O)[O-])c3F)c(=O)oc2c1
Reaction #687029
title compound
Ausbeute 42.6%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)Oc1ccc2c(CF)c(Cc3cccc([N+](=O)[O-])c3F)c(=O)oc2c1
Reaction #687030
title compound
Ausbeute 70.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Cc2cccc(/N=C\c3ccccc3)c2F)c(=O)oc2cc(Oc3nccs3)ccc12
Reaction #687031
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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