Teilstruktursuche

CC(C)C(=O)N

Cl.NC1(C(=O)Nn2cccc2)CC1
Reaction #50660
product
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](c4csc(N)n4)C3)[C@H](C)[C@H]12
Reaction #65562
(4R,5S,6S)-3-[(2S,4S)-2-(2-aminothiazol-4-yl) -pyrrolidin-4-ylthio]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo [3.2.0]hept-2-ene-2-carboxylic acid
Ausbeute 45.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C1CCN(c2nccc3nc(NCc4ccccc4Cl)ncc23)CC1)N1CCN(CCO)CC1
Reaction #69763
solid
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C1CCN(C(=O)[C@@H]2CCCN(c3cccc(-c4nc5ccccc5n4C)c3)C2)CC1
Reaction #164288
title compound
Ausbeute 74.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(NC(=O)NCC(=O)N2C(C(=O)OC(C)(C)C)CC(C(=O)N(C)C)C2c2ccccc2)c1
Reaction #185288
DOI: 10.1039/C8SC04228D
CCC1CC1(NC(=O)C1CC(OC(=O)N2Cc3cccc(Cl)c3C2)CN1C(=O)C(Nc1cc(F)cc(C(F)(F)F)c1)C(C)(C)C)C(=O)NS(=O)(=O)C1CC1
Reaction #186614
DOI: 10.1039/C8SC04228D
Cl
Reaction #187513
DOI: 10.1039/C8SC04228D
COCOc1ccc(-c2ccc3c(c2CN(C(=O)OCC2c4ccccc4-c4ccccc42)c2ccccc2OC)N(C)C(=O)C(C)(C)N3)c(OC)c1
Reaction #192526
DOI: 10.1039/C8SC04228D
CC(C)[Si](OCCC1(CCN2CCCC2)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(CC2CC2)C1=O)(C(C)C)C(C)C
Reaction #205296
DOI: 10.1039/C8SC04228D
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2CCCCN2)C1=O
Reaction #220132
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@H](Oc3ccccc3)CN2)C1=O
Reaction #220133
title compound
Ausbeute 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@H](Oc3ccccn3)CN2)C1=O
Reaction #220135
title compound
Ausbeute 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@H](Oc3ccccn3)CN2)C1=O
Reaction #220136
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](Oc3ccccc3)CN2)C1=O
Reaction #220138
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](Oc3ccccn3)CN2)C1=O
Reaction #220140
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](Oc3ccccn3)CN2)C1=O
Reaction #220141
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](Oc3cccnc3)CN2)C1=O
Reaction #220143
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](Oc3cccnc3)CN2)C1=O
Reaction #220144
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](O)CN2)C1=O
Reaction #220146
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](O)CN2)C1=O
Reaction #220147
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
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