Поиск подструктуры

11185

CCOc1ccc(C2(Br)C=CC=CC2)c(F)c1F
Reaction #7430
formula 13
DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2ccccc2-c2ccccc2)cc1
Reaction #7431
terphenyl
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1COc2c(N3CCN(C)CC3)c(F)cc3c(=O)c(C(=O)O)cn1c23
Reaction #8583
crystals
Выход 51.9%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #10417
ethyl acetate hexanes
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N2CC[C@H]([C@@H](C)NC(=O)OC(C)(C)C)C2)c(F)cc2c(=O)n(N)c(=O)n(C3CC3)c12
Reaction #10426
title compound
Выход 96.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)Cn1ccc(NC(=O)[C@H](CC2CCCCC2)N2CC(Oc3cccc(F)c3F)=CC2=O)n1
Reaction #47512
(S)-3-cyclohexyl-2-[4-(2,3-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-propionamide
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1CCC(C2CCc3cc(B(O)O)c(F)c(F)c3O2)CC1
Reaction #61370
7,8-difluoro-6-dihydroxyboryl-2-(4-propylcyclohexyl)chroman
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(C(=O)O)c(F)c1F
Reaction #84051
polymer-bound title compound
Выход 235.9%DOI: 10.6084/m9.figshare.5104873.v1
CCn1nc(CC(=O)N2CCCC2)cc1NC(=O)C(F)(F)F
Reaction #90776
product
Выход 44.3%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc(Nc2ncc(F)c(Nc3cc4c(F)c(F)c3OCO4)n2)c1
Reaction #158758
N4-(3,4-difluoromethylenedioxyphenyl)-5-fluoro-N2-(3-hydroxyphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161951
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methylalanyl-N-[(3R,4S,5S)-3-methoxy-5-methyl-1-oxo-1-(pentafluorophenoxy)heptan-4-yl]-N-methyl-L-valinamide
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161983
#174
Выход 92.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)[C@@]1(C)CCCN1C)C(C)C
Reaction #161992
compound #197
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)Oc1c(F)c(F)c(F)c(F)c1F)OC)N(C)C(=O)[C@@H](NC(=O)[C@]1(C)CCCN1C)C(C)C
Reaction #161995
compound #204
Выход 125.1%DOI: 10.6084/m9.figshare.5104873.v1
Oc1cccc(Nc2ncc(F)c(Nc3cc4c(F)c(F)c3OCO4)n2)c1
Reaction #163869
N4-(3,4-difluoromethylenedioxyphenyl)-5-fluoro-N2-(3-hydroxyphenyl)-2,4-pyrimidinediamine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN(C2CC(F)(F)CCNC2=O)S(=O)(=O)c2ccc(Cl)cc2)c(F)c1F
Reaction #188401
DOI: 10.1039/C8SC04228D
CCCCCC1CCc2c3c(c(F)c(F)c2O1)OC(C1CCC(CCC)CC1)C=C3
Reaction #193516
DOI: 10.1039/C8SC04228D
CC(=O)CCCC(=O)Oc1c(F)c(F)c(F)c(F)c1F
Reaction #201549
DOI: 10.1039/C8SC04228D
O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(C(=O)O)c(F)c1F
Reaction #205482
DOI: 10.1039/C8SC04228D
Fc1c(F)c(F)c(OC(F)(F)C(F)(F)C(F)(F)OC(F)(F)C2(F)OC2(F)F)c(F)c1F
Reaction #212495
DOI: 10.1039/C8SC04228D
Страница 1Далее