Substructure Search

3729

CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)N(CCC)CCC)c2)C1
Reaction #49234
title compound
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #49235
crude product
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2CC(O)(c3ccccc3)CN2)c1
Reaction #49236
title compound
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cc(C)cc(C(=O)N3CCC[C@@H]3COC)c2)C1
Reaction #49239
title compound
Yield 95.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC(NC(=O)C1CC2CCCCC2N1C(=O)C(NC(=O)C(NC(=O)c1cnccn1)C1CCCCC1)C(C)(C)C)C(O)C(=O)OCC
Reaction #70196
32
Yield 82.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N(CCC(c1ccccc1)c1cc(Br)ccc1OCc1ccccc1)C(C)C
Reaction #78872
title compound
Yield 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1CCC[C@@]1(C[C@@H](O)[C@@H](N)Cc1ccccc1)C(N)=O.N#N
Reaction #82373
N2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide
Yield 98.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)N1C[C@@H](O)C[C@@]1(C[C@@H](O)[C@@H](N)Cc1ccccc1)C(N)=O.N#N
Reaction #82386
N2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-4(S)-hydroxy-L-prolinamide
Yield 98.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(N2CCC(N(C(=O)c3ccc(-c4cnco4)cc3)C3CC3)CC2)nc1
Reaction #156008
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCOc1cnc(N2CCC(N(C(=O)c3ccc(-c4cnco4)cc3)C3CC3)CC2)nc1
Reaction #156052
N-Cyclopropyl-4-oxazol-5-yl-N-[1-(5-propoxy-pyrimidin-2-yl)-piperidin-4-yl]-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cnc(N2CCC(N(C(=O)c3ccc(-c4cnco4)cc3)C3CC3)CC2)nc1
Reaction #156053
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(C)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(CC)CO)C1=O
Reaction #176060
DOI: 10.1039/C8SC04228D
Cc1cccc(C)c1C(=O)OCC(=O)C(CC(=O)OC(C)(C)C)NC(=O)C1CCC2CC=CCC(NC(=O)c3ccc4ccccc4c3)C(=O)N21
Reaction #187282
DOI: 10.1039/C8SC04228D
CC1(CC(=O)O)CC(c2cccc(Cl)c2)C(c2ccc(Cl)cc2)N(C(C=O)CCC=O)C1=O
Reaction #197809
DOI: 10.1039/C8SC04228D
CCC(CO)N1C(=O)CCC(c2cccc(Cl)c2)C1c1ccc(Cl)cc1
Reaction #203507
DOI: 10.1039/C8SC04228D
O=C(CC(c1ccccc1)c1ccccc1)NC1CC(C(=O)O)N(C(c2ccccc2)c2ccccc2)C1
Reaction #207618
DOI: 10.1039/C8SC04228D
CCC(COCC1(C(N)=O)CC1)N1C(=O)C(CC(=O)O)CC(c2cccc(Cl)c2)C1c1ccc(Cl)cc1
Reaction #212074
DOI: 10.1039/C8SC04228D
CC(C)N(CCC(c1ccccc1)c1cc(Br)ccc1OCc1ccccc1)C(C)C
Reaction #218952
title compound
Yield 76.7%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cn(C(C)(C)C)c2nc(N3CC4CCC(C3)N4C(=O)C(F)(F)F)c(F)cc2c1=O
Reaction #225700
DOI: 10.1039/C8SC04228D
OC1(C2CCC(c3cc(F)c(F)c(F)c3)N2)CC1
Reaction #227807
DOI: 10.1039/C8SC04228D
Page 1Next