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Cc1c(C(=O)CCCl)sc2ccc(F)cc12
Reaction #276964
DOI: 10.1039/C8SC04228D
Cc1c(C=O)sc2ccc(F)cc12
Reaction #396951
DOI: 10.1039/C8SC04228D
Cc1c(C(=O)O)sc2cc(Cl)c(F)cc12
Reaction #1036309
DOI: 10.1039/C8SC04228D
CNCc1sc2ccc(F)cc2c1C
Reaction #1036524
DOI: 10.1039/C8SC04228D
Cc1csc2cc(Cl)c(F)cc12
Reaction #1045581
DOI: 10.1039/C8SC04228D
Cc1c(C=O)sc2ccc(F)cc12
Reaction #1449219
title compound
Ausbeute 98.2%DOI: 10.6084/m9.figshare.5104873.v1
CNCc1sc2ccc(F)cc2c1C
Reaction #1449220
(5-Fluoro-3-methyl-benzo[b]thiophen-2-ylmethyl)methylamine
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1sc2ccc(F)cc2c1C
Reaction #1627952
DOI: 10.1039/C8SC04228D
O=C1NCCc2c1sc1ccc(F)cc21
Reaction #1931126
product
Ausbeute 19.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccncc1N1CCc2c(sc3ccc(F)cc23)C1=O
Reaction #1931127
product
Ausbeute 37.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)C(C)(C)C)sc2ccc(F)cc12
Reaction #2190962
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(C(=O)CCCl)sc2ccc(F)cc12
Reaction #2316441
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1sc2ccc(F)cc2c1C
Reaction #2316442
titled compound
DOI: 10.6084/m9.figshare.5104873.v1