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CC(NCCN)O

CC1C(=O)N2C(CCCN3CCC4(CC4)C(O)C3)COC2(C)CN1C(=O)Nc1ccc(Cl)c(Cl)c1
Reaction #262891
DOI: 10.1039/C8SC04228D
CC(C)(ON=C(C(=O)NC1C(=O)N2C1CSC1CC(=O)OC12C(=O)[O-])c1csc(N)n1)C(=O)O
Reaction #273149
DOI: 10.1039/C8SC04228D
O=C(NC1CON(C2(C(=O)OCc3ccc([N+](=O)[O-])cc3)OC(=O)c3ccccc32)C1=O)OCc1ccccc1
Reaction #276844
DOI: 10.1039/C8SC04228D
CCN(CC)CCN1C(=O)c2ccccc2C1(O)c1cccc2ccccc12
Reaction #286752
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(C)(C)OCC1(C)C(=O)NCC(=O)c1ccc(OCCCCCCc2ccccc2)c(C(F)(F)F)c1
Reaction #291919
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C(C)(C)OCC1(C)C(=O)NCC(=O)c1ccc(O)c(C(F)(F)F)c1
Reaction #302310
DOI: 10.1039/C8SC04228D
COc1cc2c(cc1OC)C(COCCN1CCN(c3ccccc3OC)CC1)OCCC2
Reaction #310425
1-[2-[(1,3,4,5-tetrahydro-7,8-dimethoxy-2-benzoxepin-1-yl)methoxy]ethyl]-4-(2-methoxyphenyl)piperazine
Выход 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COCc1cc(C(N)C(=O)NC2(OC)C(=O)N3C(C(=O)OCOC(=O)C(NC(=O)OC(C)(C)C)C(C)C)=C(C)CSC32)ccc1O
Reaction #312504
7-[[amino[4-hydroxy-3-(methoxymethyl)phenyl]acetyl]amino]-7-methoxy-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, N-tert-butoxycarbonyl-2-amino-3-methylbutyryloxymethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCN1C(=O)c2ccccc2C1(O)c1cccc2ccccc12
Reaction #319041
2-(2-diethylaminoethyl)-3-hydroxy-3-(1-naphthyl)isoindolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCN1C(=O)c2ccccc2C1c1ccccc1C(=O)O
Reaction #319044
2-[2-(2-diethylaminoethyl)isoindolin-1-on-3-yl]benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OC[C@@H](NC(=O)OCc3ccccc3)C2=O)O1
Reaction #319375
subject compound ( 8 )
Выход 75.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OC[C@@H](NC(=O)OCc3ccccc3)C2=O)O1
Reaction #319376
subject Compound ( 8 )
Выход 24.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OC[C@H](NC(=O)OCc3ccccc3)C2=O)O1
Reaction #319377
subject Compound ( 9 )
Выход 29.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OC[C@H](NC(=O)OCc3ccccc3)C2=O)O1
Reaction #319378
subject Compound ( 9 )
Выход 5.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OC[C@@H](NC(=O)OCc3ccccc3)C2=O)O1
Reaction #319385
subject Compound ( 8 )
Выход 56.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@@H]1CON(C2(C(=O)OCc3ccccc3)C=CC(=O)O2)C1=O
Reaction #319389
subject Compound ( 32 )
Выход 20.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@H]1CON(C2(C(=O)OC(c3ccccc3)c3ccccc3)C=CC(=O)O2)C1=O
Reaction #319394
subject Compound ( 51 )
Выход 71.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@H]1CON(C2(C(=O)OC(c3ccccc3)c3ccccc3)C=CC(=O)O2)C1=O
Reaction #319395
subject Compound ( 51 )
Выход 42.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NCCSC1CC(=O)OC1(C(=O)OCc1ccc([N+](=O)[O-])cc1)N1OC[C@H](NC(=O)Cc2ccccc2)C1=O
Reaction #319401
subject Compound ( 71 )
Выход 57.3%DOI: 10.6084/m9.figshare.5104873.v1
COC1CC(C(=O)OCc2ccc([N+](=O)[O-])cc2)(N2OC[C@H](NC(=O)OCc3ccccc3)C2=O)OC1=O
Reaction #319412
subject Compound ( 94 )
Выход 47.4%DOI: 10.6084/m9.figshare.5104873.v1
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