Teilstruktursuche

CC(C)(C)OC(=O)NOC(=O)OC(C)(C)C

CCc1nc2cc(Cl)c(Cl)cc2n1-c1ccc(CCN(O)C(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #78715
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N(OC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #240907
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccncc2)sc(-c2ccncc2)c1CN(OC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #295478
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)ON(CC#Cc1cccc(C2=NC(c3ccccc3)CO2)c1F)C(=O)OC(C)(C)C
Reaction #375735
DOI: 10.1039/C8SC04228D
COc1ccc(SCCC(=O)N(OC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #467259
title compound
Ausbeute 98.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)ON(C(=O)CC(=O)C1CCN(C(=O)OC(C)(C)C)CC1)C(=O)OC(C)(C)C
Reaction #730731
tert-butyl 4-(3-{(tert-butoxycarbonyl)[(tert-butoxycarbonyl)oxy]amino}-3-oxopropanoyl)piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C=Cc1cccc(Oc2ccccc2)c1)N(OC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #791993
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(O)C(C)/C=C/c1cccc(Oc2ccccc2)c1
Reaction #791994
hydroxylamine
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(Cl)c(Cl)cc2n1-c1ccc(CCN(OC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #811274
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(Cl)c(Cl)cc2n1-c1ccc(CCNO)cc1
Reaction #811275
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C#Cc1cccc(C2CC(c3ccc(F)cc3)=NO2)c1)NO
Reaction #828872
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)ON(C/C=C\c1cccc(C2=NOC(c3ccc(F)cc3)C2)c1)C(=O)OC(C)(C)C
Reaction #828876
title compound ( 16 )
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1
ONC/C=C\c1cccc(C2=NOC(c3ccc(F)cc3)C2)c1
Reaction #828877
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nc3cc(Cl)cc(C#CCN(O)C(=O)OC(C)(C)C)c3o2)cc1OC1CCCC1
Reaction #923691
DOI: 10.1039/C8SC04228D
COc1ccc(-c2nc3cc(Cl)cc(C#CCN(O)C(=O)OC(C)(C)C)c3o2)cc1OC1CCCC1
Reaction #929314
title compound
Ausbeute 57.3%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(Cl)c(Cl)cc2n1-c1ccc(CCN(OC(=O)OC(C)(C)C)C(=O)OC(C)(C)C)cc1
Reaction #945633
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(Cl)c(Cl)cc2n1-c1ccc(CCNO)cc1
Reaction #945634
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC/C(=C/CNO)c1ccc2c(Cc3ccccc3)c(CC)oc2c1
Reaction #985535
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc2cc(Cl)c(Cl)cc2n1-c1ccc(CCN(O)C(=O)NS(=O)(=O)c2ccc(C)cc2)cc1
Reaction #1040032
DOI: 10.1039/C8SC04228D
Cc1c(-c2ccncc2)sc(-c2ccncc2)c1CN(OC(=O)OC(C)(C)C)C(=O)OC(C)(C)C
Reaction #1091362
subtitle compound
Ausbeute 35.6%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter