بحث البنية الفرعية

1350296

O=C(Nc1ccccc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #68891
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(F)cc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #68896
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1227162
DOI: 10.1039/C8SC04228D
O=C(Nc1ccccc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1841398
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(F)cc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1841403
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccccc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1904280
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(F)cc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1904285
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1ccc(-c2cccs2)cc1NC(=O)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1994934
title compound 315
المردود 16.8%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2cccs2)cc1NC(=O)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #1994935
title compound 316
المردود 64.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(Oc2ccc([N+](=O)[O-])cc2F)cc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #2019680
4-piperonylpiperazine-1-carboxylic acid [4-(2-fluoro-4-nitrophenoxy)phenyl]amide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(F)cc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #2398941
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(Oc2ccc([N+](=O)[O-])cc2F)cc1)N1CCN(Cc2ccc3c(c2)OCO3)CC1
Reaction #2400869
DOI: 10.1039/C8SC04228D