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409

CCOC(=O)c1coc(Nc2cc(Cl)ccn2)n1
Reaction #474
Ausbeute 37.0%
CCOC(=O)c1coc(N)n1
Reaction #42612
ethyl 2-amino-1,3-oxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(NS(C)(=O)=O)n1
Reaction #42613
ethyl 2-[(methylsulfonyl)amino]-1,3-oxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N(C)S(C)(=O)=O)n1
Reaction #42614
ethyl 2-[methyl(methylsulfonyl)amino]-1,3-oxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(c1nc(C(=O)O)co1)S(C)(=O)=O
Reaction #42615
2-[methyl(methylsulfonyl)amino]-1,3-oxazole-4-carboxylic acid
Ausbeute 82.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(NC(C)=O)n1
Reaction #68781
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)Nc1nc(C(=O)O)co1
Reaction #68782
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)n1
Reaction #71880
title compound
Ausbeute 79.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N2CC[C@H](N)[C@H](OC)C2)n1
Reaction #71881
title compound
Ausbeute 102.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)n1
Reaction #71882
title compound
Ausbeute 59.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C(=O)O)co3)C[C@H]2OC)nc1Cl
Reaction #71883
title compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)oc1C
Reaction #71894
title compound
Ausbeute 78.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](N)[C@H](OC)C2)oc1C
Reaction #71895
title compound
Ausbeute 113.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C(=O)O)c(C)o3)C[C@H]2OC)nc1Cl
Reaction #71896
title compound
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)oc1CC
Reaction #71916
title compound
Ausbeute 108.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](N)[C@H](OC)C2)oc1CC
Reaction #71917
title compound
Ausbeute 107.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)oc1CC
Reaction #71918
title compound
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C(=O)O)c(CC)o3)C[C@H]2OC)nc1Cl
Reaction #71919
title compound
Ausbeute 63.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)oc1C(C)C
Reaction #71921
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](N)[C@H](OC)C2)oc1C(C)C
Reaction #71922
title compound
Ausbeute 96.1%DOI: 10.6084/m9.figshare.5104873.v1
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