Ähnlichkeitssuche

399009

C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](C)C(=O)Nc1ccc2c(c1)C=CCN2C.[I-]
Reaction #417802
1-Methyl-6-(N-carbobenzoxy-L-alanyl-L-alanylamino) quinoline Iodide
Ausbeute 90.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN1CC=Cc2cc(NC(=O)[C@H](Cc3ccccc3)NC(=O)OCc3ccccc3)ccc21.[Br-]
Reaction #417803
XVI
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCCC(NC(=O)c1ccccc1)C(=O)Nc1ccc2ncccc2c1
Reaction #768765
DOI: 10.1039/C8SC04228D
O=C(O)CCCCCC(NC(=O)OCc1ccccc1)C(=O)Nc1ccccc1
Reaction #892907
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(CC(=O)OCc1ccccc1)C(=O)NC(CCc1ccc(C(F)(F)F)cc1)C(=O)Nc1ccc2ncccc2c1
Reaction #1031359
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)CCCCCC(N)C(=O)Nc1ccc2ncccc2c1
Reaction #1293675
DOI: 10.1039/C8SC04228D
O=C(O)CCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)Nc1ccccc1
Reaction #1333436
52
Ausbeute 120.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)Nc1ccc2ncccc2c1
Reaction #1356010
compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1356011
thick oil
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCC[C@H](NC(=O)c1ccccc1)C(=O)Nc1ccc2ncccc2c1
Reaction #1356012
product
Ausbeute 78.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)Nc1ccccc1
Reaction #1480811
52
Ausbeute 120.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)Nc1ccccc1
Reaction #1723077
52
Ausbeute 120.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCC[C@H](NC(=O)OCc1ccccc1)C(=O)Nc1ccc2ncccc2c1
Reaction #1802251
compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #1802252
thick oil
Ausbeute 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCC[C@H](NC(=O)c1ccccc1)C(=O)Nc1ccc2ncccc2c1
Reaction #1802253
product
Ausbeute 78.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H](CC(=O)OCc1ccccc1)C(=O)N[C@H](CCc1ccc(C(F)(F)F)cc1)C(=O)Nc1ccc2ncccc2c1
Reaction #2011151
benzyl (3S)-3-{[(tert-butoxy)carbonyl]amino}-3-{[(1R)-1-[(quinolin-6-yl)carbamoyl]-3-[4-(trifluoromethyl)phenyl]propyl]carbamoyl}propanoate
Ausbeute 82.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1nc2ccccc2cc1-c1cnc([C@H](CCCCCC(=O)OC(C)(C)C)NC(=O)OCc2ccccc2)[nH]1
Reaction #2289725
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CON(C)C(=O)[C@H](CCCCCC(=O)OC(C)(C)C)NC(=O)OCc1ccccc1
Reaction #2289728
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCCCC[C@@H](C=O)NC(=O)OCc1ccccc1
Reaction #2289729
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc2ccccc2cc1C(=O)CNC(=O)[C@H](CCCCCC(=O)OC(C)(C)C)NC(=O)OCc1ccccc1
Reaction #2289740
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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