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891672

COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3c(F)cc(F)cc3F)ccc2c1
Reaction #177131
DOI: 10.1039/C8SC04228D
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccccc2F)ccc2cc(OCc3ccccc3)ccc12
Reaction #186211
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3cc(F)c(F)cc3OC)ccc2c1
Reaction #189264
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccc(F)cc3SC)ccc2c1
Reaction #253817
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3cc(F)ccc3F)ccc2c1
Reaction #263562
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3c(F)ccc(F)c3F)ccc2c1
Reaction #374947
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(OS(=O)(=O)C(F)(F)F)ccc2c1
Reaction #397649
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(OS(=O)(=O)C(F)(F)F)ccc2c1
Reaction #404866
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(Cc3ccc(F)cc3)ccc2c1
Reaction #755137
DOI: 10.1039/C8SC04228D
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(-c2ccc(F)cc2F)ccc2cc(OCc3ccccc3)ccc12
Reaction #770795
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(OS(=O)(=O)C(F)(F)F)ccc2c1
Reaction #819984
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccc(S(C)(=O)=O)cc3)ccc2c1
Reaction #819985
title compound
Ausbeute 104.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(OS(=O)(=O)C(F)(F)F)ccc2c1
Reaction #836118
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccc(S(C)(=O)=O)cc3)ccc2c1
Reaction #836119
title compound
Ausbeute 104.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(OS(=O)(=O)C(F)(F)F)ccc2c1
Reaction #1004043
trifluoro-methanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)-benzoyl]-naphthalen-2-yl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccccc3CO)ccc2c1
Reaction #1004044
[2-(2-hydroxymethyl-phenyl)-6-methoxy-naphthalen-1-yl]-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone
Ausbeute 31.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc3cc(OC)ccc3c2C(=O)c2ccc(OCCN3CCCCC3)cc2)c(CO)c1
Reaction #1004050
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3ccc(F)cc3F)ccc2c1
Reaction #1042057
DOI: 10.1039/C8SC04228D
O=C(c1ccc(OCCN2CCCCC2)cc1)c1c(OS(=O)(=O)C(F)(F)F)ccc2cc(OCc3ccccc3)ccc12
Reaction #1225868
DOI: 10.1039/C8SC04228D
COc1ccc2c(C(=O)c3ccc(OCCN4CCCCC4)cc3)c(-c3c(F)cccc3F)ccc2c1
Reaction #1231025
DOI: 10.1039/C8SC04228D
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