子结构搜索

1414738

O=C1c2ccc([N+](=O)[O-])cc2C(=O)N1CSc1ccncc1
Reaction #6242
desired compound
收率 63.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(CO)N1Cc2ccc([N+](=O)[O-])cc2C1
Reaction #9820
2-(1,1-dimethyl-2-hydroxyethyl)-5-nitro-2,3-dihydro-1H-isoindol
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(C(CC(=O)NO)N2C(=O)c3ccc(N)cc3C2=O)ccc1OC
Reaction #9939
3-(4-aminophthalimido)-3-(3-ethoxy-4-methoxyphenyl)-N-hydroxypropionamide
收率 102.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(C(CC(=O)NOCc2ccccc2)N2C(=O)c3ccc([N+](=O)[O-])cc3C2=O)ccc1OC
Reaction #9942
N-benzyloxy-3-(3-ethoxy-4-methoxyphenyl)-3-(4-nitrophthalimido)-propionamide
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O)C1(C)OCCO1
Reaction #10937
Methyl 3-(5-nitro-1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-(2-methyl-[1,3]dioxolan-2-yl)propionate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O)C1(C)OCCO1
Reaction #10949
desired product
收率 83.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O)C(C)=O
Reaction #10970
Methyl 2-(5-nitro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(CN1C(=O)c2ccc([N+](=O)[O-])cc2C1=O)C(C)=O
Reaction #10984
Ethyl 2-(5-nitro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-3-oxo-butyrate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CC[C@@H](C(=O)OCC)N1C(=O)c2ccc(N)cc2C1=O
Reaction #52176
diethyl (S)-2-(4-aminophthalimido)glutarate
收率 88.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(F)(F)F.O=[N+]([O-])c1ccc2c(c1)CNC2
Reaction #69682
5-nitro-2,3-dihydro-1H-isoindole trifluoroacetic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C(=O)N2Cc3ccc([N+](=O)[O-])cc3C2)c(OCc2ccccc2)cc1OCc1ccccc1
Reaction #69702
(2,4-bis-benzyloxy-5-isopropyl-phenyl)-(5-nitro-1,3-dihydro-isoindol-2-yl)methanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1cc(C(=O)N2Cc3ccc(N)cc3C2)c(OCc2ccccc2)cc1OCc1ccccc1
Reaction #69703
(5-amino-1,3-dihydro-isoindol-2-yl)-(2,4-bis-benzyloxy-5-isopropyl-phenyl)-methanone
收率 87.7%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2c(cc1[N+](=O)[O-])C(=O)NC2=O
Reaction #156526
5-Amino-6-nitroisoindoline-1,3-dione
收率 92.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2c(cc1[N+](=O)[O-])C(=O)N(c1cccnc1)C2=O
Reaction #156527
5-Amino-6-nitro-2-(pyridine-3-yl)isoindoline-1,3-dione
收率 62.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc2c(cc1[N+](=O)[O-])C(=O)N(c1ccc(F)nc1)C2=O
Reaction #156529
5-Amino-2-(6-fluoropyridin-3-yl)-6-nitroisoindoline-1,3-dione
收率 12.7%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N)c([N+](=O)[O-])cc2c1C(=O)N(CCN(C)C)C2=O
Reaction #156537
designed compound
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(N)c(N)cc2c1C(=O)N(CCN(C)C)C2=O
Reaction #156538
5,6-Diamino-2-(2-(dimethylamino)ethyl)-4-methylisoindoline-1,3-dione
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
收率 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
收率 29.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1C(=O)c2cc(Cl)c([N+](=O)[O-])cc2C1=O
Reaction #156547
5-Chloro-2-isopropyl-6-nitroisoindoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
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