Substructure Search

5540

COc1cccc(C(=O)N(CCOC2CCCCO2)c2ccccc2OC)c1
Reaction #2558
title compound
Yield 67.0%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(NC2CCN(CCOC3CCCCO3)CC2)c2ccncc2c1
Reaction #10679
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc2cccc(NC3CCN(CCO)CC3)c12.Cl
Reaction #10680
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.OCCN[C@H]1CC[C@H](Nc2cccc3cnccc23)CC1
Reaction #10681
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc2cccc(N[C@H]3CC[C@H](NCCO)CC3)c12.Cl
Reaction #10682
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.OCCN[C@H]1CC[C@@H](Nc2cccc3cnccc23)CC1
Reaction #10683
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cncc2cccc(N[C@H]3CC[C@@H](NCCO)CC3)c12.Cl
Reaction #10684
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1cncc2cccc(O[C@H]3CC[C@H](NCCO)CC3)c12
Reaction #10685
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)cc(C=Cc1ccccc1Cl)n2CCO
Reaction #11135
2-{2-[2-(2-Chlorophenyl)ethenyl]-5-methoxy-1H-indol-1-yl}ethanol
Yield 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)cc(C=Cc1c(Cl)cccc1OC)n2CCO
Reaction #11149
2-{2-[2-(2-Chloro-6-methoxyphenyl)ethenyl]-5-methoxy-1H-indol-1-yl}ethanol
Yield 91.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)c1c3c(c(-c4ccccc4)cc1n2CCO)C(=O)NC3=O
Reaction #11157
6-(2-Hydroxyethyl)-9-methoxy-4-phenylpyrrolo[3,4-c]carbazole-1,3(2H,6H)-dione
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(COCCOC4CCCCO4)nc3N21
Reaction #12037
(4R,9aR)-4-Methyl-6-[2-(tetrahydro-pyran-2-yloxy)-ethoxymethyl]-3,4,9,9a-tetrahydro-1H-2,4a,5-triaza-fluorene-2-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
Ic1cnn(CCOC2CCCCO2)c1
Reaction #44295
4-iodo-1-[2-(tetrahydro-pyran-2-yloxy)-ethyl]-1H-pyrazole
Yield 87.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)OC(C)(C)C)[C@H]1CC[C@H](C#CCCOC2CCCCO2)CC1
Reaction #53921
trans-Methyl-{4-[4-(tetrahydro-pyran-2-yloxy)-but-1-ynyl]-cyclohexyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c(/C=C/c3ccc(F)cc3)nn2C(=O)OC(C)(C)C)c1OCCOC1CCCCO1
Reaction #62326
title compound
Yield 56.5%DOI: 10.6084/m9.figshare.5104873.v1
Ic1cnn(CCOC2CCCCO2)c1
Reaction #69788
4-Iodo-1-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)-1H-pyrazole
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(OCCOC2CCCCO2)cc1[N+](=O)[O-]
Reaction #86489
title compound
Yield 38.2%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncc2c(c1OC1CCN(CCOC3CCCCO3)CC1)c1cc(Br)cnc1n2S(=O)(=O)c1ccccc1
Reaction #88607
title compound
Yield 33.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nn(CCOC2CCCCO2)cc1I
Reaction #88952
title compound
Yield 39.0%DOI: 10.6084/m9.figshare.5104873.v1
Ic1cnn(CCOC2CCCCO2)c1
Reaction #156396
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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