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CC1(C)NCCS1

CC(C)CC=C1CCC2(CC1)SC(CC(=O)OC(C)C)C(=O)N2CC(=O)OC(C)(C)C
Reaction #173328
DOI: 10.1039/C8SC04228D
CC(C)CC=C1CCC2(CC1)SCC(=O)N2CCC(=O)O
Reaction #175927
DOI: 10.1039/C8SC04228D
CCC1(C(=O)O)NCCS1
Reaction #177047
DOI: 10.1039/C8SC04228D
OCCSC1CN=C(c2ccccc2)c2cc(Cl)ccc2N1
Reaction #191490
DOI: 10.1039/C8SC04228D
CC(C)c1ccc(OC2CCC3(CC2)SCC(C(=O)NCCC(=O)O)N3C(=O)c2ccccc2)cc1
Reaction #196472
DOI: 10.1039/C8SC04228D
CCOC(=O)CC1SC2(CCNCC2)N(CCc2ccccc2)C1=O
Reaction #211925
DOI: 10.1039/C8SC04228D
O=C(C(Cl)Cl)N1CCSC12CCCCC2
Reaction #214665
product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C(Cl)Cl)N1CCSC12CCCC2
Reaction #214668
N-dichloroacetyl-1-thia-4-azaspiro[4,4]nonane
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2cccnc2)NC(C(=O)O)CS1
Reaction #216908
2-methyl-2-(3-pyridyl)thiazolidine-4- carboxylic acid
Ausbeute 37.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CSC(c2ccccn2)(c2ccccn2)N1
Reaction #216909
2,2-di(2-pyridyl)-thiazolidine-4-carboxylic acid
Ausbeute 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)SCCN1C(=O)C(Br)Br
Reaction #225874
DOI: 10.1039/C8SC04228D
CC(C)c1ccc(OC2CCC3(CC2)NC(C(=O)O)C(C)(C)S3)cc1
Reaction #258728
DOI: 10.1039/C8SC04228D
CC(C)c1ccc(NC(=O)C2CCC3(CC2)SCC(C(=O)O)N3C(=O)c2ccccc2)cc1
Reaction #262081
DOI: 10.1039/C8SC04228D
CC(C)CC=C1CCC2(CC1)SC(=Cc1ccccc1)C(=O)N2CCC(=O)O
Reaction #265465
DOI: 10.1039/C8SC04228D
CS(=O)c1c(C2(C)NCCS2)nn(-c2c(Cl)cc(C(F)(F)F)cc2Cl)c1N
Reaction #268639
DOI: 10.1039/C8SC04228D
CC(C)CC=C1CCC2(CC1)SC(CC(=O)OC(C)C)C(=O)N2CC(=O)O
Reaction #288005
DOI: 10.1039/C8SC04228D
CC(C)c1ccc(OC2CCC3(CC2)SCC(C(=O)NCCC(=O)OCc2ccccc2)N3C(=O)c2ccccc2)cc1
Reaction #295822
DOI: 10.1039/C8SC04228D
CC1(C)SCCN1C(=O)C(Br)Br
Reaction #312409
2,2-dimethyl-3-dibromoacetyl thiazolidine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1CCCCC1)NC1CCCCC1
Reaction #324030
dicyclohexylurea
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)SCCN1C(=S)[S-].CC1(C)SCCN1C(=S)[S-].[Zn+2]
Reaction #354722
Zinc Bis(2,2-dimethylthiazolidine-3-carbodithioate)
DOI: 10.6084/m9.figshare.5104873.v1
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