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O=Cc1ccccc1O

CN1CCC(Oc2ccc(Cl)cc2C(N)=O)C1.CN1CCC(Oc2ccc(Cl)cc2C(N)=O)C1.O
Reaction #4877
product
Ausbeute 34.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC2CC2)c(C=O)cc1-c1cccs1
Reaction #10735
2-Cyclopropylmethoxy-4-methoxy-5-thiophen-2-yl-benzaldehyde
Ausbeute 18.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC2CC2)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10736
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(CO)CO)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10782
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(N)=O)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10789
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(CO)CO)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10805
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc2sc(N3CCN(C(=O)c4cc(S(C)(=O)=O)ccc4OC(C)C)CC3)nc12
Reaction #61432
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3CN3CCOCC3)cc1)cn2C1CCOC1
Reaction #79765
5-[4-(2-morpholinomethylphenoxy)phenyl] -7-(3-tetrahydrofuryl)-7H-pyrrolo[2,3-d]pyrimidin-4-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
COCCNCc1ccccc1Oc1ccc(-c2cn(C3CCOC3)c3ncnc(N)c23)cc1
Reaction #79766
5-{4-[2-(2-methoxyethyl)aminomethylphenoxy]phenyl}-7-(3-tetrahydrofuryl)-7H-pyrrolo[2,3-d]-pyrimidin-4-ylamine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(C(F)(F)F)c(SC)c1O
Reaction #87869
4-trifluoromethyl-3-methylthio-2-hydroxybenzoic acid ethyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(Nc2ncc(F)c(Nc3ccc(C(=O)O)c(O)c3)n2)cc1O
Reaction #158719
N2,N4-bis(3-hydroxy-4-carboxyphenyl)-5-fluoro-2,4-pyrimidinediamine
Ausbeute 78.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(Nc2ncc(F)c(Nc3ccc(C(=O)O)c(O)c3)n2)cc1O
Reaction #163830
N2,N4-bis(3-hydroxy-4-carboxyphenyl)-5-fluoro-2,4-pyrimidinediamine
Ausbeute 78.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Br)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1C[C@H]1CCCO1
Reaction #165673
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)c1s/c(=N\C(=O)c2cc(Cl)ccc2OCC(F)(F)F)n(C[C@H]2CCCO2)c1C
Reaction #165697
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1C[C@@H]1CCCO1
Reaction #165707
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(Cl)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1Cc1cc(C)on1
Reaction #165722
title compound
Ausbeute 46.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccccc2C=O)C1
Reaction #172297
tert-butyl 3-(2-formylphenoxy)pyrrolidine-1-carboxylate
Ausbeute 23.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(Oc2ccccc2-c2nc3c(C(=O)O)cccc3[nH]2)C1
Reaction #172298
titled compound 31
Ausbeute 84.4%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1c(-c1ccc(Oc3ccccc3CN3CCOCC3)cc1)cn2C1CCOC1
Reaction #179938
DOI: 10.1039/C8SC04228D
CCOc1cc(OCC)c2c(c1)S(=O)(=O)N(COc1cc(C(F)(F)F)nn1-c1ccccc1)C2=O
Reaction #190291
DOI: 10.1039/C8SC04228D
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