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CC(=O)NCC1CN(c2ccc(-c3ccc(COC4COc5nc([N+](=O)[O-])cn5C4)s3)c(F)c2)C(=O)O1
Reaction #262406
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2ccc(-c3ccc(OCC4(C)Cn5cc([N+](=O)[O-])nc5O4)cc3)c(F)c2)C(=O)O1
Reaction #267022
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2ccc(-c3ccc(C4=NOC(CO)C4)nc3)c(F)c2)C(=O)O1
Reaction #274042
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2ccc(B3OC(C)(C)C(C)(C)O3)c(F)c2)C(=O)O1
Reaction #360442
N-{3-[3-fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}acetamide
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(c2ccc(-c3ccc(N4CC(CNC(C)=O)OC4=O)cc3F)cc2)Cn2cc([N+](=O)[O-])nc2O1
Reaction #406869
DOI: 10.1039/C8SC04228D
CC(=O)NC[C@H]1CN(c2ccc(B3OC(C)(C)C(C)(C)O3)c(F)c2)C(=O)O1
Reaction #428335
(5S)—N-{3-[3-fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}acetamide
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc(-c3ccc(CN(CCCF)C(=O)OC(C)(C)C)cc3)c(F)c2)C(=O)O1
Reaction #428336
(5S)-{4′-[5-(acetylamino-methyl)-2-oxo-oxazolidin-3-yl]-2′-fluoro-biphenyl-4-ylmethyl}-(3-fluoro-propyl)-carbamic acid tert-butyl ester
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc(-c3ccc(C4=NO[C@H](CO)C4)nc3)c(F)c2)C(=O)O1
Reaction #546199
title compound
Ausbeute 48.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc(-c3ccc(C4=NO[C@@H](CO)C4)nc3)c(F)c2)C(=O)O1
Reaction #546201
N-{[(5S)-3-(3-Fluoro-4-{6-[(5R)-5-(hydroxymethyl)-4,5-dihydroisoxazol-3-yl]pyridin-3-yl}phenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCC1CN(c2ccc(B3OC(C)(C)C(C)(C)O3)c(F)c2)C(=O)O1
Reaction #733133
N-{3-[3-fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}acetamide
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCC1CN(c2ccc(B3OC(C)(C)C(C)(C)O3)c(F)c2)C(=O)O1
Reaction #945060
N-{3-[3-fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}acetamide
Ausbeute 94.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCC1CN(c2ccc(B3OC(C)(C)C(C)(C)O3)c(F)c2)C(=O)O1
Reaction #1232042
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2ccc(-c3ccc(N4CCN(C(=O)OC(C)(C)C)CC4)nc3)c(F)c2)C(=O)O1
Reaction #1290346
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2cc(F)c(-c3ccc(OC4COc5nc([N+](=O)[O-])cn5C4)nc3)c(F)c2)C(=O)O1
Reaction #1304313
DOI: 10.1039/C8SC04228D
CC(=O)NCC1CN(c2ccc(-c3ccc(OCC4(C)Cn5cc([N+](=O)[O-])nc5O4)cc3)c(F)c2)C(=O)O1
Reaction #1533250
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc(-c3cnc(OCC4(C)Cn5cc([N+](=O)[O-])nc5O4)nc3)c(F)c2)C(=O)O1
Reaction #1533256
title compound
Ausbeute 39.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc(-c3ccc(CO[C@@H]4COc5nc([N+](=O)[O-])cn5C4)s3)c(F)c2)C(=O)O1
Reaction #1533264
titled compound
Ausbeute 48.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NC[C@H]1CN(c2ccc(-c3ccc(N4CCN(C(=O)OC(C)(C)C)CC4)nc3)c(F)c2)C(=O)O1
Reaction #1533265
titled compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCC1CN(c2cc(F)c(-c3ccc(OC4COc5nc([N+](=O)[O-])cn5C4)nc3)c(F)c2)C(=O)O1
Reaction #1533269
title product
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
C=CCC1(c2ccc(-c3ccc(N4CC(CNC(C)=O)OC4=O)cc3F)cc2)Cn2cc([N+](=O)[O-])nc2O1
Reaction #1533279
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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