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1163924

CCOC(=O)CC[C@@H](C(=O)OCC)N1C(=O)c2ccc(N)cc2C1=O
Reaction #52176
diethyl (S)-2-(4-aminophthalimido)glutarate
Ausbeute 88.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@@H](C(=O)OCC)N1Cc2cc(N)ccc2C1=O
Reaction #52177
Diethyl (S)-2-(5-amino-1-oxo-2-isoindolinyl)glutarate
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2c(cc1[N+](=O)[O-])C(=O)N(C[C@@H](O)CO)C2=O
Reaction #156544
solid
Ausbeute 83.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1nccc(Cl)c1-c1nc2cc3c(cc2[nH]1)C(=O)N(C[C@@H](O)CO)C3=O
Reaction #156545
title compound
Ausbeute 29.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O
Reaction #184111
DOI: 10.1039/C8SC04228D
CCOC(=O)CCC(C(=O)OCC)N1Cc2cc(N)ccc2C1=O
Reaction #283868
DOI: 10.1039/C8SC04228D
CCOC(=O)CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O
Reaction #337646
title compound
Ausbeute 611.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1C(=O)c2ccc(N)cc2C1=O
Reaction #337647
title compound
Ausbeute 78.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1C(=O)c2ccc(N=C(c3ccccc3)c3ccccc3)cc2C1=O
Reaction #337648
title compound
Ausbeute 52.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1C(=O)c2ccc(Oc3cc(F)cc(F)c3)cc2C1=O
Reaction #337667
[5-(3,5-Difluoro-phenoxy)-1,3-dioxo-1,3-dihydro-isoindol-2-yl]-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1C(=O)c2ccc(Oc3ccc(Oc4ccc(F)cc4)cc3)cc2C1=O
Reaction #337668
{5-[4-(4-Fluoro-phenoxy)-phenoxy]-1,3-dioxo-1,3-dihydro-isoindol-2-yl}-acetic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@@H](C(=O)OCC)N1C(=O)c2ccc(N)cc2C1=O
Reaction #364879
diethyl (S)-2-(4-aminophthalimido)glutarate
Ausbeute 88.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@@H](C(=O)OCC)N1Cc2cc(N)ccc2C1=O
Reaction #364880
Diethyl (S)-2-(5-Amino-1-oxo-2-isoindolinyl)glutarate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CCC(C(=O)OCC)N1Cc2cc(N)ccc2C1=O
Reaction #392667
DOI: 10.1039/C8SC04228D
O=C(Cl)CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O
Reaction #443337
(4-nitrophthalimido)acetyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O
Reaction #443387
titled compound
Ausbeute 77.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@@H](C(=O)OCC)N1C(=O)c2ccc([N+](=O)[O-])cc2C1=O
Reaction #468764
diethyl(S)-2-(4-nitrophthalimido)glutarate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@@H](C(=O)OCC)N1C(=O)c2ccc(N)cc2C1=O
Reaction #468765
diethyl(S)-2-(4-aminophthalimido)glutarate
Ausbeute 88.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@@H](C(=O)OCC)N1Cc2cc(N)ccc2C1=O
Reaction #468766
diethyl(S)-2-(5-amino-1-oxo-2-isoindolinyl)glutarate
Ausbeute 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O
Reaction #496474
title compound
Ausbeute 89.8%DOI: 10.6084/m9.figshare.5104873.v1
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