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564933

CC(C)COc1ccc(CN2C(=O)CC3(CCN(C(=O)OC(C)(C)C)CC3)N2Cc2ccc(F)cc2)cc1
Reaction #40651
desired compound
Ausbeute 50.6%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1N(C(=O)OCc2ccccc2)C(O)CC1(C)C
Reaction #302027
DOI: 10.1039/C8SC04228D
CCN1N(c2ccc(I)cn2)C(=O)CC1(C)C
Reaction #327669
1-ethyl-2-(5-iodo-pyridin-2-yl)-5,5-dimethyl-pyrazolidin-3-one
Ausbeute 28.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)NN2Cc1ccc(F)cc1
Reaction #836461
desired compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COc1ccc(CN2C(=O)CC3(CCN(C(=O)OC(C)(C)C)CC3)N2Cc2ccc(F)cc2)cc1
Reaction #836462
desired compound
Ausbeute 50.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COc1ccc(CN2C(=O)CC3(CCN(C(=O)OC(C)(C)C)CC3)N2Cc2ccc(F)cc2)cc1
Reaction #985467
desired compound
Ausbeute 50.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)NN2Cc1ccc(F)cc1
Reaction #1159743
desired compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COc1ccc(CN2C(=O)CC3(CCN(C(=O)OC(C)(C)C)CC3)N2Cc2ccc(F)cc2)cc1
Reaction #1159744
desired compound
Ausbeute 50.6%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1NC(=O)CC1(C)C
Reaction #1224515
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)NN2Cc1ccc(F)cc1
Reaction #1438421
desired compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COc1ccc(CN2C(=O)CC3(CCN(C(=O)OC(C)(C)C)CC3)N2Cc2ccc(F)cc2)cc1
Reaction #1438422
desired compound
Ausbeute 50.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)NN2Cc1ccc(F)cc1
Reaction #1874903
desired compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COc1ccc(CN2C(=O)CC3(CCN(C(=O)OC(C)(C)C)CC3)N2Cc2ccc(F)cc2)cc1
Reaction #1874904
desired compound
Ausbeute 50.6%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1NC(=O)CC1(C)C
Reaction #2148800
103
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1N(C(=O)OCc2ccccc2)C(O)CC1(C)C
Reaction #2148801
105
Ausbeute 76.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC2(CC1)CC(=O)NN2Cc1ccc(F)cc1
Reaction #2397615
DOI: 10.1039/C8SC04228D