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27741

COCCn1ccc2nccc(Sc3ccc([N+](=O)[O-])cc3)c21
Reaction #180956
DOI: 10.1039/C8SC04228D
CC(CC#N)COC(C)(C)C
Reaction #294672
DOI: 10.1039/C8SC04228D
Brc1n[nH]c2cnccc12
Reaction #476770
title compound
Ausbeute 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(C(F)(F)F)cnc1Br
Reaction #532097
title product
DOI: 10.6084/m9.figshare.5104873.v1
COCCn1ccc2nccc(Sc3ccc([N+](=O)[O-])cc3)c21
Reaction #590789
1-(2-methoxyethyl)-7-(4-nitrophenylthio)-1H-pyrrolo[3,2-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=S(=O)(c1ccc(Cl)cc1)c1cnc2cc(Cl)ccc2c1Br
Reaction #648227
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(Br)c(S(=O)(=O)c3ccc(F)c(F)c3)cnc2c1
Reaction #648230
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(C(F)(F)F)cnc1Br
Reaction #661406
title product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cnc(Br)c2cn(-c3c(Cl)cccc3Cl)nc12
Reaction #713959
title compound
Ausbeute 38.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(C(F)(F)F)cnc1Br
Reaction #975033
title product
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(C(F)(F)F)cnc1Br
Reaction #1024522
DOI: 10.1039/C8SC04228D
CC(=O)O[C@@H]1[C@@H](OCc2ccccc2)OC[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #1052045
3
Ausbeute 96.1%DOI: 10.6084/m9.figshare.5104873.v1
COCCn1ccc2nccc(Sc3ccc([N+](=O)[O-])cc3)c21
Reaction #1100914
1-(2-methoxyethyl)-7-(4-nitrophenylthio)-1H-pyrrolo[3,2-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COCCn1ccc2nccc(Sc3ccc([N+](=O)[O-])cc3)c21
Reaction #1130054
1-(2-methoxyethyl)-7-(4-nitrophenylthio)-1H-pyrrolo[3,2-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N2CCOCC2)cc(C(C)=O)cc1C(C)(C)C
Reaction #1383136
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(Br)ccn(CC2CC2)c1=O
Reaction #1487386
intermediate 8
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(Br)ccn(CCC2CC2)c1=O
Reaction #1487387
intermediate 9
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCn1ccc(Br)c(C#N)c1=O
Reaction #1487388
intermediate 10
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nn(-c2ccccc2)c(Br)c1C=O
Reaction #1609029
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc2c(Br)c(S(=O)(=O)c3ccc(F)c(F)c3)cnc2c1
Reaction #2225563
DOI: 10.1039/C8SC04228D
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