Substructure Search

O=C1CSCN1

CC(C)c1cc(C=C2SCN(C)C2=O)cc(C(C)C)c1O
Reaction #3031
5-[[3,5-bis(1-methylethyl)-4-hydroxyphenyl]methylene]-3-methyl-4-thiazolidinone
DOI: 10.6084/m9.figshare.5104873.v1
CCN(C)N1CSC(=Cc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)C1=O
Reaction #3042
desired product
Yield 29.8%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)N1C(=O)C(=CCc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)SC1=S
Reaction #3044
5-[[3,5-bis(1,1-dimethylethyl) -4-hydroxyphenyl]methylmethylene]-3-(dimethylamino)-2-thioxo-4-thiazolidinone
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCN1C(=O)CSC1CCCc1ccc(C(=O)OCC)cc1
Reaction #56482
title compound
Yield 31.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCC(O)CCN1C(=O)CSC1CCCc1ccc(C(=O)O)cc1
Reaction #56483
desired title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccccc2)SC(=S)N(Nc2ccccc2)C1=O
Reaction #79494
5-methyl-5-phenyl-3-phenylamino-2-thioxothiazolidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccccc2)SC(=NO)N(Nc2ccccc2)C1=O
Reaction #79497
2-hydroxyimino-5-methyl-5-phenyl-3-phenylaminothiazolidine-4-one
Yield 70.2%DOI: 10.6084/m9.figshare.5104873.v1
CON=C1SC(C)(c2ccccc2)C(=O)N1Nc1ccccc1
Reaction #79498
2-methoxyimino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one
Yield 41.9%DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccccc2)SC(=Nc2ccc(Cl)cc2)N(Nc2ccccc2)C1=O
Reaction #79499
2-(4-chlorophenyl)imino-5-methyl-5-phenyl-3-phenylaminothiazolidin-4-one
Yield 57.8%DOI: 10.6084/m9.figshare.5104873.v1
CCn1c(COc2ccc(CC3SC(=O)N(C(c4ccccc4)(c4ccccc4)c4ccccc4)C3=O)cc2)nc2cccnc21
Reaction #83763
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(COc2ccc(CC3SC(=O)N(C(c4ccccc4)(c4ccccc4)c4ccccc4)C3=O)cc2)nc2ccc(Cl)nc21
Reaction #83771
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(COc2ccc(CC3SC(=O)N(C(c4ccccc4)(c4ccccc4)c4ccccc4)C3=O)cc2)nc2cc(Cl)cnc21
Reaction #83787
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1C(=Cc2ccccc2)SC(=S)N1N=c1sc2ccccc2s1
Reaction #175164
DOI: 10.1039/C8SC04228D
CCOC(=O)C=C1SC(c2ccccc2)N(CCC(C)C)C1=O
Reaction #177765
DOI: 10.1039/C8SC04228D
CN(CCCN1C(=O)C(CCO)SC1c1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1)CCOc1ccc2c(c1)OCO2
Reaction #179661
DOI: 10.1039/C8SC04228D
COc1ccc(CC2SC(=O)NC2=O)c2c1N(Cc1ccc(N)cc1)C(=O)CC2
Reaction #179901
DOI: 10.1039/C8SC04228D
O=C1NC(=S)SC1Cc1cccc2c1CCC(=O)N2Cc1ccc(Br)cc1
Reaction #182856
DOI: 10.1039/C8SC04228D
O=C1NC(=O)C(Cc2cn(Cc3ccc(O)cc3)c3ccccc23)S1
Reaction #184701
DOI: 10.1039/C8SC04228D
Cn1c(COc2ccc(CC3SC(=O)NC3=O)cc2)nc2ccc(Oc3ccc(NC(=O)c4ccc5ccccc5c4)cc3)cc21
Reaction #187694
DOI: 10.1039/C8SC04228D
COc1ccc(CC2SC(=O)NC2=O)c2c1N(CC1CCN(C3CCOCC3)CC1)C(=O)CC2
Reaction #196175
DOI: 10.1039/C8SC04228D
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