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COCC=O

Cc1cc(SCc2sc(-c3ccc(C(F)(F)F)c(F)c3)nc2C)ccc1OCC(=O)O
Reaction #6941
final product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc(C(C)=O)cc1C
Reaction #9722
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C)(C)Oc1ccc(OC(C)=O)cc1C
Reaction #9723
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OCC(=O)N2CCOCC2)c(/C=C/C(=O)c2ccc(C(=O)O)cc2)cc1-c1cccs1
Reaction #10790
title compound
Ausbeute 70.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(Cc2ccc(F)cc2)[C@@H](C)CN1C(=O)COc1ccc(Cl)cc1NS(=O)(=O)CC(=O)O
Reaction #11730
(5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-phenylsulfamoyl)-acetic acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C1c2ccccc2C(=O)C1Cc1n[nH]c(=S)[nH]c1=O
Reaction #46259
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)nc(C(F)(F)F)n1
Reaction #48084
yellow oil
Ausbeute 66.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@H](C)Nc1ccc(Cl)c(Cl)c1
Reaction #51305
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(Nc1ccc(Cl)c(Cl)c1)C(=O)OCC(C)C
Reaction #51316
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(Nc1ccc(Cl)c(Cl)c1)C(=O)OCC(C)C
Reaction #51319
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@H](C)Nc1ccc(Cl)cc1
Reaction #51320
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@H](C)Nc1cc(Cl)cc(Cl)c1
Reaction #51321
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@H](C)Nc1ccc(N=[N+]=[N-])cc1
Reaction #51326
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)COC(=O)[C@H](C)Nc1ccc2ccccc2c1
Reaction #51329
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc2cc(N[C@@H](C)C(=O)OCC(C)C)ccc2n1
Reaction #51330
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)COc1ccc(C(C)C)cc1CN1CCN(S(=O)(=O)c2ccccc2)CC1
Reaction #66571
sub-title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)c1ccc(OCC(=O)[O-])c(CN2CCN(S(=O)(=O)c3ccccc3)CC2)c1.[Na+]
Reaction #66572
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(OCC(=O)NNc3ccc(Cl)nn3)ccnc2c1
Reaction #68453
N′-(6-chloropyridazin-3-yl)-2-(7-methoxyquinolin-4-yloxy)acetohydrazide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(OCc3nnc4ccc(Cl)nn34)ccnc2c1
Reaction #68454
4-((6-chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methoxy)-7-methoxyquinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)C=C(C)OCC
Reaction #70768
ethyl 4-ethoxy-2-oxopent-3-enoate
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
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