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1272611

CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@H]1COS(=O)(=O)c1ccc(C)cc1
Reaction #43301
intermediate 45
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)(C)c1ccc(C2(O)CCCN(Cc3ccccc3)C2)c(OCc2ccccc2)c1
Reaction #54339
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(C)(C)c1ccc(C2(O)CCCNC2)c(O)c1
Reaction #54340
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #55889
2,3-dehydro-1-(3-acetylthio-1-oxopropyl)-5-methoxypipecolic acid
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)OC(C)(C)C)CC[C@@H]1NC(=O)c1ncc[nH]1
Reaction #71714
title compound
Ausbeute 58.0%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
CCCCOC(=O)c1nc(N2CC[C@H](N)[C@H](OCCC)C2)oc1C
Reaction #71943
title compound
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCCC)C2)oc1C
Reaction #71944
title compound
Ausbeute 44.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](N)[C@H](OC)C2)oc1CCC
Reaction #71952
title compound
Ausbeute 96.8%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)oc1CCC
Reaction #71953
title compound
Ausbeute 44.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3cc(OC)cc(C(=O)OC)c3)C[C@H]2OC)nc1Cl
Reaction #72242
title compound
Ausbeute 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3ccc(OC)c(C(=O)OC)c3)C[C@H]2OC)nc1Cl
Reaction #72245
title compound
Ausbeute 58.2%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1(O)CN2CCC1CC2
Reaction #76782
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CC1(O)CN2CCC1CC2
Reaction #77879
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(CNc2nc(Cl)cc3nccnc23)CC(O[Si](C)(C)C(C)(C)C)C1
Reaction #85815
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(O)CC(CNc2nc(Cl)cc3nccnc23)C1
Reaction #85816
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(F)CC(CNc2nc(Cl)cc3nccnc23)C1
Reaction #85817
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CC(=O)CC(CNc2nc(Cl)cc3nccnc23)C1
Reaction #85818
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(=O)C(CNc2nc(Cl)cc3nccnc23)C1
Reaction #85824
tert-butyl 3-((7-chloropyrido[4,3-b]pyrazin-5-ylamino)methyl)-4-oxopiperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
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