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c1ccc2c(c1)Sc1ccccc1S2

O=C(O)c1ccc2c(c1)Sc1cccc(Br)c1S2
Reaction #62062
6-Bromo-thianthrene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)Sc1cccc(Br)c1S2
Reaction #62063
6-Bromo-thianthrene-2-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc2c(c1)Sc1cccc(-c3cc(=O)cc(N4CCOCC4)o3)c1S2
Reaction #62064
6-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-thianthrene-2-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])c1ccc2c(c1)Sc1cccc(-c3cc(=O)cc(N4CCOCC4)o3)c1S2.[Na+]
Reaction #62065
6-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-thianthrene-2-carboxylate sodium salt
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(c1)Sc1cccc(Br)c1S2
Reaction #62068
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)Sc1cccc(Br)c1S2
Reaction #62069
title compound
Ausbeute 104.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc2c(c1)Sc1cccc(-c3cc(=O)cc(N4CCOCC4)o3)c1S2
Reaction #62070
title compound
Ausbeute 127.4%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc2c(c1)Sc1cccc(-c3cc(=O)cc(N4CCOCC4)o3)c1S2
Reaction #62071
2-(7-Amino-thianthren-1-yl)-6-morpholin-4-yl-pyran-4-one
DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc2c1Sc1ccccc1S2
Reaction #62072
title compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc(Br)c2c1Sc1ccccc1S2
Reaction #62073
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCOc1ccc(Br)c2c1Sc1ccccc1S2
Reaction #62074
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCOc1ccc(-c2cc(=O)cc(N3CCOCC3)o2)c2c1Sc1ccccc1S2
Reaction #62075
title compound
Ausbeute 101.6%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2ccc(O)c3c2Sc2ccccc2S3)oc(N2CCOCC2)c1
Reaction #62076
2-(4-Hydroxy-thianthren-1-yl) -6-morpholin-4-yl-pyran-4-one
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #62077
solid
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])COc1ccc(-c2cc(=O)cc(N3CCOCC3)o2)c2c1Sc1ccccc1S2.[Na+]
Reaction #62078
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2cccc3c2Sc2ccc(O)cc2S3)oc(N2CCOCC2)c1
Reaction #62087
title compound
Ausbeute 100.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])COc1ccc2c(c1)Sc1cccc(-c3cc(=O)cc(N4CCOCC4)o3)c1S2.[Na+]
Reaction #62088
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COCOc1ccc(Br)c2c1Sc1ccccc1S2
Reaction #183659
DOI: 10.1039/C8SC04228D
O=c1cc(-c2cccc3c2Sc2ccc(O)cc2S3)oc(N2CCOCC2)c1
Reaction #186138
DOI: 10.1039/C8SC04228D
Oc1cccc2c1Sc1ccccc1S2
Reaction #228194
DOI: 10.1039/C8SC04228D
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