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199176

CCOC(=O)c1sc(NOC(=O)OC(C)(C)C)nc1C
Reaction #9183
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NOC(=O)OC(C)(C)C)sc1C(=O)O
Reaction #9184
2-tert-butoxycarbonyloxyamino-4-methyl-thiazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(NOC(=O)OC(C)(C)C)nc1C(F)(F)F
Reaction #9186
title compound
Ausbeute 92.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)ONc1nc(C(F)(F)F)c(C(=O)O)s1
Reaction #9187
2-Tert-butoxycarbonyloxyamino-4-trifluoromethyl-thiazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(NOC(=O)OCc2ccccc2)nc1C
Reaction #9188
title compound
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(NS(C)(=O)=O)nc1C
Reaction #9189
title compound
Ausbeute 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(NOC(=O)OC(C)(C)C)nc1C
Reaction #9191
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)ONc1ncc(C(=O)O)s1
Reaction #9192
2-tert-butoxycarbonyloxyamino-thiazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nc(N)sc1C(=O)OC
Reaction #71727
title compound
Ausbeute 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)nc1C(=O)N1CCN(C)CC1
Reaction #71786
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N(C(=O)OC(C)(C)C)C(=O)OC(C)(C)C)nc1C(O)CC
Reaction #71789
title compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)O
Reaction #71800
title compound
Ausbeute 99.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)NCCOC
Reaction #71801
title compound
Ausbeute 72.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)NC
Reaction #71806
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@H]1CN(c2nc(C(=O)NCCOC)c(C(=O)OCC)s2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71808
title compound
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](NC(=O)OCc3ccccc3)C2)nc1C
Reaction #71817
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](N)C2)nc1C
Reaction #71818
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(-n2ccc(N3CC[C@H](NC(=O)c4nc(Cl)c(CC)[nH]4)[C@H](OCC)C3)cc2=O)nc1C
Reaction #72006
title compound
Ausbeute 6.5%DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1CN(c2ccn(-c3nc(C)c(C(=O)O)s3)c(=O)c2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72007
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC(C)C)C2)nc1C(=O)NCCOC
Reaction #72020
title compound
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
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