Teilstruktursuche

250135

CC(=O)Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2ccccc2C(F)(F)F)cc1
Reaction #2581
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N(CCN2CCC(C(=O)c3ccc(F)cc3)CC2)c2cccnc2)cc1)c1ccccc1
Reaction #2615
title compound
Ausbeute 71.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cccc(Nc2nc3cc(Oc4ccnc(C(=O)NCCNS(=O)(=O)Cc5ccccc5)c4)ccc3n2C)c1
Reaction #41787
4-[2-(3-Isopropyl-phenylamino)-1-methyl-1H-benzoimidazol-5-yloxy]-pyridine-2-carboxylic acid (2-phenylmethanesulfonylamino-ethyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2C(=O)CC[C@@H]2/C=C(\c2ccc(C(C)(C)C)cc2)c2ccc(N)c(OC)n2)c(OC)c1
Reaction #157828
(5R)-5-[(E)-2-(5-amino-6-methoxypyridin-2-yl)-2-(4-tert-butylphenyl)ethenyl]-1-(2,4-dimethoxybenzyl)pyrrolidin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1nc(/C(=C/[C@H]2CCC(=O)N2)c2ccc(C(C)(C)C)cc2)ccc1N
Reaction #157829
(5R)-5-[(E)-2-(5-amino-6-methoxypyridin-2-yl)-2-(4-tert-butylphenyl)ethenyl]pyrrolidin-2-one
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #158169
solid
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(n1cnn(-c2ccc(OCC(F)(F)C(F)(F)F)cc2)c1=O)C1(c2ccc(F)cc2F)CO1
Reaction #177393
DOI: 10.1039/C8SC04228D
Cc1cc(C(O)(C(F)(F)F)C(F)(F)F)cc(C)c1NC(=O)c1cccc(NC(=O)c2ccccc2)c1
Reaction #185800
DOI: 10.1039/C8SC04228D
O=C(Nc1cccc(Oc2ccc3nc(NC(=O)C4CC4)[nH]c3c2)c1)c1cccc(C(F)(F)F)c1
Reaction #187094
DOI: 10.1039/C8SC04228D
Cl
Reaction #187513
DOI: 10.1039/C8SC04228D
CC(C)N1CCC(Oc2cc3cc(C(=O)N4CCN(C(=O)C5CC5)CC4)[nH]c3cc2Br)CC1
Reaction #188624
DOI: 10.1039/C8SC04228D
O=C(Nc1cc(-c2ccccc2)ccc1O)c1ccc(C(C(=O)Nc2ccccc2)C(=O)Nc2ccccc2)cc1
Reaction #189628
DOI: 10.1039/C8SC04228D
CC(=O)c1cccc(OC(CCN2CCC(c3ccc(C)c(NC(=O)C(C)C)c3)CC2)c2ccccc2)c1
Reaction #202957
DOI: 10.1039/C8SC04228D
COC(=O)NCC1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #205365
DOI: 10.1039/C8SC04228D
COc1c2ccc(NC(C)=O)cc2nn1CC(C)(C#N)NC(=O)c1ccc(OC(F)(F)F)cc1
Reaction #205848
DOI: 10.1039/C8SC04228D
CC(C)(C)c1cc(NC(=O)Nc2ccc(C(=O)N3CCN(Cc4ccc(C(O)(C(F)(F)F)C(F)(F)F)cc4)CC3)cc2F)no1
Reaction #209445
DOI: 10.1039/C8SC04228D
CC(C)C(NC(=O)Cn1c(-c2ccccc2)ccc(NC(=O)NCc2ccccc2)c1=O)(O[SiH](C)C)C(C(C)(C)C)C(F)(F)F
Reaction #211463
DOI: 10.1039/C8SC04228D
C[C@@H](n1ccn(-c2ccc(OCC(F)(F)C(F)(F)F)cc2)c1=O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216332
1-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-3-[4-(2,2,3,3,3-pentafluoropropoxy)phenyl]-2(1H,3H)-imidazolone
Ausbeute 22.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](n1nnn(-c2ccc(OCC(F)(F)C(F)(F)F)cc2)c1=O)[C@@]1(c2ccc(F)cc2F)CO1
Reaction #216354
1-[(1R,2S)-2-(2,4-difluorophenyl)-2,3-epoxy-1-methylpropyl]-4-[4-(2,2,3,3,3-pentafluoropropoxy)phenyl]-5(1H,4H)-tetrazolone
Ausbeute 69.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)c1ccc(NC(=O)Nc2cc(C#N)cnc2Oc2ccccc2C(C)(C)C)cc1
Reaction #219788
solid
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter