部分構造検索

1434715

O=C(CSc1nc[nH]n1)c1ccc(OCc2c(F)cccc2F)cc1
Reaction #53294
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(Cc1ccc(CCOc2ccc(OS(C)(=O)=O)cc2)cc1)SCCc1ccc(OCc2ccccc2)cc1
Reaction #62094
desired product
収率 80.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(Cc2ccc(OCc3ccc(Cl)cc3)cc2)S1
Reaction #177106
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(Cc2ccc(OCc3cccc(-c4ccccc4)c3)cc2)S1
Reaction #179698
DOI: 10.1039/C8SC04228D
CCSC(Cc1ccc(OCc2ccccc2)cc1)C(=O)OC
Reaction #180264
DOI: 10.1039/C8SC04228D
CCSC(Cc1ccc(O)cc1)C(=O)OC
Reaction #183996
DOI: 10.1039/C8SC04228D
O=C(CSc1nc[nH]n1)c1ccc(OCc2c(F)cccc2F)cc1
Reaction #208675
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(OCc2ccccc2)cc1)Sc1ncc(-c2ccccc2)[nH]1
Reaction #209637
DOI: 10.1039/C8SC04228D
COCOc1cccnc1SC(C)C(O)c1ccc(OCc2ccc(OC)cc2)cc1
Reaction #223090
DOI: 10.1039/C8SC04228D
CCOS(=O)(=O)CCc1ccc(O)cc1
Reaction #265690
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(OCc2ccccc2)cc1)SC1=NS(=O)(=O)c2ccccc21
Reaction #280772
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc(CCOc2ccc(OS(C)(=O)=O)cc2)cc1)SCCc1ccc(O)cc1
Reaction #283937
DOI: 10.1039/C8SC04228D
O=C1SC(Cc2ccc(OCc3ccc4c(c3)ncn4Cc3ccccc3)cc2)C(=O)N1C(c1ccccc1)(c1ccccc1)c1ccccc1
Reaction #289562
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(Cc2ccc(OCc3ccccc3)c3c2CCC(=O)N3Cc2ccccc2)S1
Reaction #293097
DOI: 10.1039/C8SC04228D
O=C(CSc1nc[nH]n1)c1ccc(OCc2c(F)cccc2F)cc1
Reaction #338729
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1Cc2cc(N3CC(=O)NS3(=O)=O)c(OCc3ccccc3)cc2S1
Reaction #387575
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(Cc2ccc(OCc3ccc(Cl)cc3)cc2)S1
Reaction #413339
5-[4-(4-chlorobenzyloxy)benzyl]thiazolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1NC(=O)C(Cc2ccc(OCc3ccc(Cl)cc3)cc2)S1
Reaction #413343
5-[4-(4-chlorobenzyloxy)benzyl]thiazolidine-2,4-dione
収率 24.4%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #562711
solid
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CSc1nc[nH]n1)c1ccc(OCc2c(F)cccc2F)cc1
Reaction #583895
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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