Recherche de Similitude

C(CS)S

O=S(=O)(c1cccc2cnccc12)N1Cc2cc(O)c(O)cc2CC1CN1CCN(c2ccccc2)CC1
Reaction #5816
title compound
Rendement 90.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CO)ccc(C#N)c1Cl
Reaction #43467
title compound
Rendement 66.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)S[C@H]1C[C@@H](C2SCCS2)N(C(=O)OCc2ccc([N+](=O)[O-])cc2)C1
Reaction #65546
(2S, 4S)-4-acetylthio-2-(1,3-dithiolan-2-yl) -1-(4-nitrobenzyloxycarbonyl)pyrrolidine
DOI: 10.6084/m9.figshare.5104873.v1
CC1(c2ccccc2)OC(CC(SCCS)c2ccsc2)=CC1=O
Reaction #78302
5-[2-[(2-mercaptoethyl)thio]-2-(3-thienyl)ethyl]-2-methyl-2-phenylfuran-3(2H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CC1=C(C(=O)Nc2ccc(Cl)cc2)SCCS1
Reaction #183266
DOI: 10.1039/C8SC04228D
CSc1c(C2(C)SCCS2)nn(-c2c(Cl)cc(C(F)(F)F)cc2Cl)c1N
Reaction #184434
DOI: 10.1039/C8SC04228D
CCCCC1(c2cc(OC)cc(OC)c2)SCCS1
Reaction #213548
DOI: 10.1039/C8SC04228D
O=C1C2=C(NC3(C=N2)SCCS3)c2ccccc21
Reaction #216635
title compound
Rendement 64.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1C2=C(NC(=O)C3(N2)SCCS3)c2ccccc21
Reaction #216636
title compound
Rendement 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCBr)Nc1ccc([AsH2])cc1
Reaction #217484
4-(bromopropionamido)-phenylarsine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=NOC)C1=CSCCS1
Reaction #231771
DOI: 10.1039/C8SC04228D
CC(=O)OCCC1(c2ccc(F)cc2)SCCS1
Reaction #235046
DOI: 10.1039/C8SC04228D
CCCN(C)C(=O)c1cc(C(=O)OC)cc(C2(c3ccco3)SCCS2)c1
Reaction #236332
DOI: 10.1039/C8SC04228D
CC(C)(C(=O)c1ccc(SCCS)cc1)N1CCOCC1
Reaction #238211
DOI: 10.1039/C8SC04228D
COC(=O)C1CC2(CN1C(=O)OCc1ccccc1)SCCS2
Reaction #239393
DOI: 10.1039/C8SC04228D
COC(=O)Cc1ccccc1C1SCCS1
Reaction #252729
DOI: 10.1039/C8SC04228D
COC(=O)CC1SCCCS1
Reaction #273233
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(C2SCCS2)cc1
Reaction #278240
DOI: 10.1039/C8SC04228D
O=C(O)C1CC2(CN1C(=O)OCc1ccccc1)SCCS2
Reaction #281723
DOI: 10.1039/C8SC04228D
CC(n1ccnc1)C1(c2ccc(Cl)cc2Cl)SCCS1
Reaction #298902
DOI: 10.1039/C8SC04228D
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