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CC(C)(C)OC(=O)COc1cccc(C=O)c1
Reaction #52064
title compound
Ausbeute 36.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1cccc(C=NO)c1
Reaction #52065
title compound
Ausbeute 91.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1cccc(CN)c1
Reaction #52066
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1cccc(CNS(=O)(=O)c2cccnc2)c1
Reaction #52067
title compound
Ausbeute 78.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1cccc(C(=O)C=Cc2cccnc2)c1
Reaction #178937
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(C=CCOC(=O)N(c2ccccc2)c2ccccc2)c1
Reaction #186565
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(CCN)c1
Reaction #205406
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(Br)c1
Reaction #208232
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(CNCc2ccc(-c3cncnc3)cc2)c1
Reaction #209458
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(C#N)c1
Reaction #231010
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(OCCO)c1
Reaction #241882
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(C=CCO)c1
Reaction #261496
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(CNCc2ccc(C(C)(C)C)cc2)c1
Reaction #263071
DOI: 10.1039/C8SC04228D
COc1cc(CCC(O)c2cccc(OCC(=O)OC(C)(C)C)c2)cc(OC)c1OC
Reaction #270175
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(C=O)c1
Reaction #276153
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(C=CCO)c1
Reaction #278842
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(CNCc2ccc(-c3ncccn3)cc2)c1
Reaction #298094
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)COc1cccc(Oc2ccccc2)c1
Reaction #336750
t-Butyl (3-phenoxy)phenoxyacetate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1cccc(C(=O)O)c1
Reaction #365071
7-3
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)COc1ccc(C(=O)O)cc1
Reaction #373509
DOI: 10.1039/C8SC04228D
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