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1175534

Nc1cc(F)c2c(c1)CCO2
Reaction #264224
DOI: 10.1039/C8SC04228D
CCCc1nc(C)n(-c2cc(F)c3c(c2)CC(C)(C)O3)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #297029
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(F)c2c(c1)CCO2
Reaction #1293494
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1cc(F)c2c(c1)CCO2
Reaction #1603635
desired compound 7
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(F)c2c(c1)CCO2
Reaction #1603636
desired compound 8
Ausbeute 93.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCCCC1=NNc1cc(F)c2c(c1)CCO2
Reaction #1603637
desired compound 9
Ausbeute 29.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCCc2c1[nH]c1cc(F)c3c(c21)CCO3
Reaction #1603638
desired compound 10
Ausbeute 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C)n(-c2cc(F)c3c(c2)CC(C)(C)O3)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #1761293
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C)n(-c2cc(F)c3c(c2)CC(C)(C)O3)c(=O)c1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1
Reaction #1761294
title compound
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C)n(-c2cc(F)c3c(c2)CC(C)(C)O3)c(=O)c1Cc1ccc(-c2ccccc2C#N)cc1
Reaction #1805963
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C)n(-c2cc(F)c3c(c2)CC(C)(C)O3)c(=O)c1Cc1ccc(-c2ccccc2-c2noc(=O)[nH]2)cc1
Reaction #1805964
title compound
Ausbeute 71.5%DOI: 10.6084/m9.figshare.5104873.v1