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1271790

O=c1cc(Cl)oc(N2CCOCC2)c1
Reaction #62058
3
Ausbeute 75.4%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
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
COCOc1ccc(-c2cc(=O)cc(N3CCOCC3)o2)c2c1Sc1ccccc1S2
Reaction #62075
title compound
Ausbeute 101.6%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1c2ccccc2Sc2c(-c3cc(=O)cc(N4CCOCC4)o3)cccc21
Reaction #62079
solid
Ausbeute 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc2c(c1)Cc1cccc(-c3cc(=O)cc(N4CCOCC4)o3)c1S2
Reaction #62085
[5-(6-Morpholin-4-yl-4-oxo-4H-pyran-2-yl)-9H-thioxanthen-2-yl]-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2cccc3c2Oc2ccccc2S3)oc(N2CCOCC2)c1
Reaction #190420
DOI: 10.1039/C8SC04228D
O=c1cc(-c2ccc(F)c3c(=O)c4ccccc4sc23)oc(N2CCOCC2)c1
Reaction #195042
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc(-c2cc(=O)cc(N3CCOCC3)o2)c2c1Cc1ccccc1S2
Reaction #228225
DOI: 10.1039/C8SC04228D
O=c1cc(-c2cccc3c2Sc2ccccc2CC3)oc(N2CCOCC2)c1
Reaction #395274
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)Nc1ccc2c(c1)Cc1cccc(-c3cc(=O)cc(N4CCOCC4)o3)c1S2
Reaction #905771
DOI: 10.1039/C8SC04228D
O=c1cc(-c2cccc3sc4ccccc4c23)oc(N2CCOCC2)c1
Reaction #1220160
DOI: 10.1039/C8SC04228D
O=C1Cc2ccccc2Sc2c1cccc2-c1cc(=O)cc(N2CCOCC2)o1
Reaction #1289724
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(-c2cc(=O)cc(N3CCOCC3)o2)cc1
Reaction #1628211
DOI: 10.1039/C8SC04228D
O=c1cc(Cl)oc(N2CCOCC2)c1
Reaction #1852220
desired compound
Ausbeute 75.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc(-c2cc(=O)cc(N3CCOCC3)o2)c1
Reaction #1852221
title compound
Ausbeute 46.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(-c2cc(=O)cc(N3CCOCC3)o2)cc1
Reaction #1852223
title compound
Ausbeute 63.3%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(Cl)oc(N2CCOCC2)c1
Reaction #1912955
3
Ausbeute 75.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2cccc3c2Sc2ccccc2S3)oc(N2CCOCC2)c1
Reaction #1912956
title compound
Ausbeute 4.4%DOI: 10.6084/m9.figshare.5104873.v1
O=c1cc(-c2cccc3c2Oc2ccccc2S3)oc(N2CCOCC2)c1
Reaction #1912957
title compound
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
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