Поиск подструктуры

NCc1cccc(I)c1

CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2ncc[nH]2)c1
Reaction #42340
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C)C(=O)c1cc(I)cc(C(=O)OC)c1
Reaction #42343
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(C)C(=O)c1cc(C(=O)O)cc(-c2ncco2)c1
Reaction #42344
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(I)cc(C(=O)OC)c1
Reaction #42349
methyl 3-[(dipropylamino)carbonyl]-5-iodobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42350
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2nccn2COCC)c1
Reaction #42351
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCO)Cc1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(I)c2)c1.Cl.Cl
Reaction #42382
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2nccs2)c1
Reaction #42566
methyl 3-[(dipropylamino)carbonyl]-5-(1,3-thiazol-2-yl)benzoate
Выход 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(I)cc(C(=O)OC)c1
Reaction #42570
methyl 3-[(dipropylamino)carbonyl]-5-iodobenzoate
Выход 79.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42571
methyl 3-[(dipropylamino)carbonyl]-5-(1,3-oxazol-2-yl)benzoate
Выход 27.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cc(I)cc(C(=O)OC)c1
Reaction #42575
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42576
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CC)C(=O)c1cc(I)cc(C(=O)OC)c1
Reaction #42579
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CC)C(=O)c1cc(C(=O)OC)cc(-c2ncco2)c1
Reaction #42580
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C(N)=O)c(C)c(I)c1F
Reaction #45570
compound
Выход 96.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(C(N)=O)c(C)c(I)c1Br
Reaction #45571
compound
Выход 50.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(F)c(I)c(C)c(C(N)=O)c1NC(=O)C(C)C
Reaction #45585
compound
Выход 29.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C1NCc2c(Cl)ccc(I)c21
Reaction #49286
4-chloro-7-iodoisoindolinone
Выход 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)n1c(-c2ccc(Cl)c3c2C(=O)NC3)cc2ccccc21
Reaction #49287
4-chloro-7-(1-(tert-butoxycarbonyl)indol-2-yl)isoindolinone
Выход 44.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(I)c2c1CNC2=O
Reaction #49355
4-methoxy-7-iodoisoindolinone
Выход 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Страница 1Далее