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1412349

[O-][n+]1ccc2ccccc2c1
Reaction #73097
isoquinoline 2-oxide
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1nccc2ccccc12
Reaction #73098
isoquinoline-1-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1ccc2cc(F)c(Cl)cc2c1
Reaction #73459
desired product 9
Выход 87.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)Nc1nccc2cc(F)c(Cl)cc12
Reaction #73472
pure desired product ( 95 )
Выход 4.3%DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1ccc2ccc(Br)cc2c1Cl
Reaction #180374
DOI: 10.1039/C8SC04228D
[O-][n+]1cc2ccccc2cc1Cl
Reaction #198199
DOI: 10.1039/C8SC04228D
[O-][n+]1ccc2cc(F)ccc2c1
Reaction #202713
DOI: 10.1039/C8SC04228D
[O-][n+]1ccc2c(Br)cccc2c1
Reaction #207030
DOI: 10.1039/C8SC04228D
Cc1c[n+]([O-])cc2cc([N+](=O)[O-])ccc12
Reaction #226780
DOI: 10.1039/C8SC04228D
[O-][n+]1ccc2cc(F)c(Br)cc2c1
Reaction #243982
DOI: 10.1039/C8SC04228D
[O-][n+]1ccc2c(Br)cccc2c1
Reaction #359952
title compound
Выход 75.9%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1nccc2c(Br)cccc12
Reaction #359953
title compound
Выход 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc2ccccc2c(CCl)[n+]1[O-]
Reaction #437844
1-Chloromethyl-3-methyl-isoquinoline-2-oxide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2ccnc(N)c2c1Cl
Reaction #463497
title compound
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1ccc2cc(F)c(Cl)cc2c1
Reaction #489699
material
Выход 67.6%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc2ccnc(Cl)c2cc1Cl
Reaction #489700
title compound
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1ccc2cc(Br)ccc2c1
Reaction #491899
crude product
Выход 96.5%DOI: 10.6084/m9.figshare.5104873.v1
Clc1nccc2cc(Br)ccc12
Reaction #491900
title compound
DOI: 10.6084/m9.figshare.5104873.v1
[O-][n+]1ccc2cc(Br)c(Cl)cc2c1
Reaction #491905
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc2c(Cl)nccc2cc1Br
Reaction #491906
6-Bromo-1,7-dichloro-isoquinoline
DOI: 10.6084/m9.figshare.5104873.v1
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