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C1=CSC=N1

—
Reaction #40587
solid
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCON=C(C(=O)OCC)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #55540
ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetate
Ausbeute 86.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCON=C(C(=O)OCC)c1csc(N)n1
Reaction #55541
ethyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetate
Ausbeute 82.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](Cc1ccccc1)c1nccs1
Reaction #161909
#14
Ausbeute 10.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(NCCCCNC(=O)OC(C)(C)C)c1nccs1
Reaction #182772
DOI: 10.1039/C8SC04228D
CC1CCC(N(CCCc2cccc(C(F)(F)F)c2)C(=O)Nc2ncc(SCC(=O)O)s2)CC1
Reaction #189185
DOI: 10.1039/C8SC04228D
C#CCON=C(C(=O)OCC)c1csc(NC(c2ccccc2)(c2ccccc2)c2ccccc2)n1
Reaction #192673
DOI: 10.1039/C8SC04228D
CC(C)(Sc1nc(CCOc2ccc(C(=O)Nc3ccccc3)cc2)cs1)C(=O)O
Reaction #195689
DOI: 10.1039/C8SC04228D
CC(C)(C)NC(=O)CSc1nc(-c2ccc(F)cc2)cs1
Reaction #197687
DOI: 10.1039/C8SC04228D
CC(=O)SC1CN(c2nc(C(=O)N3CCN(C)CC3)cs2)C1
Reaction #199770
DOI: 10.1039/C8SC04228D
COCCCC1CN(C2=Nc3ccccc3Nc3sc(C(C)C)nc32)CCN1
Reaction #213099
DOI: 10.1039/C8SC04228D
COCC[C@H]1CN(C2=Nc3ccccc3Nc3sc(C(C)C)nc32)CCN1
Reaction #218670
title compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCC[C@H]1CN(C2=Nc3ccccc3Nc3sc(C(C)C)nc32)CCN1
Reaction #218673
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCC[C@H]1CN(C2=Nc3ccccc3Nc3sc(C(F)(F)F)nc32)CCN1
Reaction #218677
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@H](C)C[C@H]1CN(C2=Nc3ccccc3Nc3sc(C(C)C)nc32)CCN1
Reaction #218693
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCN(CCc1csc(SC(C)(C)C(=O)O)n1)c1ncc(N2CCOCC2)cn1
Reaction #222252
DOI: 10.1039/C8SC04228D
Nc1ncc(-c2ccccc2COc2ccccc2)s1
Reaction #229688
DOI: 10.1039/C8SC04228D
COCCC1CN(C2=Nc3ccccc3Nc3sc(C(C)C)nc32)CCN1
Reaction #230419
DOI: 10.1039/C8SC04228D
O=C(Nc1nc2c(s1)CCCc1ccccc1-2)c1ccncc1
Reaction #231198
DOI: 10.1039/C8SC04228D
O=C(O)COc1ccc2cc(-c3csc(Cc4c(Cl)cccc4Cl)n3)ccc2c1
Reaction #236121
DOI: 10.1039/C8SC04228D
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