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225320

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
COCCOCCOc1cc(OC)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10766
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC(C)(C)C(=O)O)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10775
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCOCCOCCOc1cc(OC)c(-c2cccs2)cc1/C=C/C(=O)c1ccc(C(=O)O)cc1
Reaction #10784
title compound
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC(C)(C)C(=O)O)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10801
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2nnn[nH]2)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10808
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCCN2CCOCC2)c(/C=C/C(=O)c2ccc(C(N)=O)cc2)cc1-c1cccs1
Reaction #10811
title compound
Ausbeute 57.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC(C)(C)C(=O)O)c(-c2cccs2)cc1/C=C/C(=O)c1ccc(NS(C)(=O)=O)cc1
Reaction #10817
title compound
Ausbeute 15.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(-c2nc3cccnc3[nH]2)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10835
title compound
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCc2nc3ccccc3[nH]2)c(/C=C/C(=O)c2ccc(S(N)(=O)=O)cc2)cc1-c1cccs1
Reaction #10836
title compound
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(C2C=CCO2)cc1/C=C/C(=O)c1ccc(S(N)(=O)=O)cc1
Reaction #10846
title compound
Ausbeute 72.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC=C1c1cc2[nH]c(-c3ccccn3)nc2cc1Oc1ccc(S(C)(=O)=O)cc1
Reaction #41667
6-(1-Acetyl-4,5-dihydro-1H-pyrrol-2-yl)-5-(4-(methanesulfonyl)phenoxy)-2-pyridin-2-yl-1H-benzimidazole
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)cc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #60541
title compound
Ausbeute 127.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(F)cc1C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #60542
title compound
Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(F)(F)F)cc1C1CCN(C(=O)OC(C)(C)C)CC1
Reaction #74601
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(F)(F)F)cc1C1=CCN(C(=O)OC(C)(C)C)CC1
Reaction #74602
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1/C=C/c1nc2ccccc2n1-c1ccccn1.O=C(O)C(=O)O
Reaction #79162
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCC)c1ccc(C=Cc2ccc(C=CC3=C(C#N)C(=C(C#N)C#N)OC3(c3ccccc3)C(F)(F)F)s2)c(OC)c1
Reaction #172423
dark brown powdered crystal
Ausbeute 92.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCC)c1ccc(C=Cc2ccc(C=CC3=C(C#N)C(=C(C#N)C#N)OC3(C)C)s2)c(OCc2ccccc2)c1
Reaction #172427
dark brown crystal
Ausbeute 58.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(CCCC)c1ccc(C=Cc2ccc(C=CC3=C(C#N)C(=C(C#N)C#N)OC3(C)C(F)(F)F)s2)c(OCc2ccccc2)c1
Reaction #172428
dark reddish brown crystal
Ausbeute 94.0%DOI: 10.6084/m9.figshare.5104873.v1
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