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1265704

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
COCOc1ccc(Br)c2c1Sc1ccccc1S2
Reaction #183659
DOI: 10.1039/C8SC04228D
Oc1cccc2c1Sc1ccccc1S2
Reaction #228194
DOI: 10.1039/C8SC04228D
O=c1cc(-c2ccc(O)c3c2Sc2ccccc2S3)oc(N2CCOCC2)c1
Reaction #287159
DOI: 10.1039/C8SC04228D
COCOc1ccc(-c2cc(=O)cc(N3CCOCC3)o2)c2c1Sc1ccccc1S2
Reaction #2243302
DOI: 10.1039/C8SC04228D