Recherche de Sous-structure

1252435

COc1cc2c3c(cccc3c1[N+](=O)[O-])C(=O)N(OCc1ccccc1)C2=O
Reaction #247454
DOI: 10.1039/C8SC04228D
O=C1c2cccc3c(N4CCCC4)c(Br)cc(c23)C(=O)N1OCc1ccccc1
Reaction #268675
DOI: 10.1039/C8SC04228D
COc1cc2c3c(cccc3c1[N+](=O)[O-])C(=O)N(OCc1ccccc1)C2=O
Reaction #366142
title compound
Rendement 75.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cccc3c(N4CCCCC4)c(Br)cc(c23)C(=O)N1OCc1ccccc1
Reaction #366146
2-benzyloxy-5-bromo-6-(piperidin-1-yl)-benzo[de]isoquinoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN(c2c(Br)cc3c4c(cccc24)C(=O)N(OCc2ccccc2)C3=O)C1
Reaction #366147
title compound
Rendement 86.9%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2c(Br)cc3c4c(cccc24)C(=O)N(OCc2ccccc2)C3=O)CC1
Reaction #366148
title compound
Rendement 38.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cccc3c(N4CCCC4)c(Br)cc(c23)C(=O)N1OCc1ccccc1
Reaction #366149
title compound
Rendement 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(c2c(Br)cc3c4c(cccc24)C(=O)N(OCc2ccccc2)C3=O)C1
Reaction #366150
title compound
Rendement 80.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CCON1C(=O)c2ccc(N3CCCC3)c3cc(Br)cc(c23)C1=O
Reaction #366154
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCON1C(=O)c2ccc(N3CCCC3)c3cc(C)cc(c23)C1=O
Reaction #366155
title compound
Rendement 96.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cccc3c([N+](=O)[O-])ccc(c23)C(=O)N1O
Reaction #366170
title compound
Rendement 72.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c3c(cccc3c1[N+](=O)[O-])C(=O)N(OCc1ccccc1)C2=O
Reaction #654153
title compound
Rendement 75.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccc(N3CCCCC3)c3cc(Br)cc(c23)C(=O)N1OCc1ccccc1
Reaction #654158
2-benzyloxy-5-bromo-7-(piperidin-1-yl)-benzo[de]isoquinoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCN(c2c(Br)cc3c4c(cccc24)C(=O)N(OCc2ccccc2)C3=O)C1
Reaction #654159
title compound
Rendement 86.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cccc3c(N4CCCC4)c(Br)cc(c23)C(=O)N1OCc1ccccc1
Reaction #654160
title compound
Rendement 90.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@H]1CCN(c2c(Br)cc3c4c(cccc24)C(=O)N(OCc2ccccc2)C3=O)C1
Reaction #654161
title compound
Rendement 80.8%DOI: 10.6084/m9.figshare.5104873.v1
C=CCON1C(=O)c2ccc(N3CCCC3)c3cc(Br)cc(c23)C1=O
Reaction #654165
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C=CCON1C(=O)c2ccc(N3CCCC3)c3cc(C)cc(c23)C1=O
Reaction #654166
title compound
Rendement 96.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2cccc3c([N+](=O)[O-])ccc(c23)C(=O)N1O
Reaction #654181
title compound
Rendement 72.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCON1C(=O)c2ccc(N3CCCC3)c3cc(Br)cc(c23)C1=O
Reaction #1236216
DOI: 10.1039/C8SC04228D
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