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9443

O=C(OC1CC(CO)C1O)c1ccccc1
Reaction #6056
title compound
Ausbeute 101.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN[C@H](Cc2c[nH]c3ccccc23)c2nc(-c3ccccc3)c[nH]2)cc1
Reaction #51646
solid
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)NC(=S)N[C@@H](CO)CCCCNC(=O)OCc1ccccc1
Reaction #76008
benzyl (5R)-5-{[(tert-butylamino)carbothioyl]amino}-6-hydroxyhexylcarbamate
Ausbeute 60.3%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H](CO)CC1CCCCC1
Reaction #76027
(2R)-2-amino-3-cyclohexyl-1-propanol
Ausbeute 105.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(Cl)cc(Br)cc1CO
Reaction #84726
title product
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(Cl)c(Br)cc1CO
Reaction #84732
title compound
Ausbeute 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(F)cc(Br)cc1CO
Reaction #84747
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CO)c(N)c1
Reaction #84758
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(N)c1nc2ccn(C)c2cc1Br
Reaction #162474
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(CO)cc1)N1CCCCC1
Reaction #173058
DOI: 10.1039/C8SC04228D
Cc1c(F)c(F)c(F)c(CO)c1F
Reaction #173120
DOI: 10.1039/C8SC04228D
CC1(CC2=Cc3cccc(-c4ccc(C(C)(C)C)cc4)c3C2)CCCCC1
Reaction #173183
DOI: 10.1039/C8SC04228D
O=[N+]([O-])CCc1ccc(Oc2ccccc2F)nc1
Reaction #173198
DOI: 10.1039/C8SC04228D
OCc1c(-c2ccc(Cl)cc2)nn(-c2ccccc2)c1Cl
Reaction #173391
DOI: 10.1039/C8SC04228D
OCc1cc2nccc(Cl)c2s1
Reaction #173488
DOI: 10.1039/C8SC04228D
Cl
Reaction #173562
DOI: 10.1039/C8SC04228D
O=C(c1ccccc1)N1CC2CC=Cc3cccc1c32
Reaction #173587
DOI: 10.1039/C8SC04228D
O=c1[nH]c2ccc(C3CCC(NCCCc4ccc(Cl)cc4)CC3)cc2o1
Reaction #173589
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2nc3ccc(C)cn3c2C2CCCN(C)C2=O)cc1
Reaction #173759
DOI: 10.1039/C8SC04228D
COc1cccc(CO)n1
Reaction #173806
DOI: 10.1039/C8SC04228D
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