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O=CC=Cc1ccccc1

CCCCOc1ccc(C(=O)n2c(C)cc3c(CCC(=O)O)cccc32)cc1
Reaction #11509
title compound
Ausbeute 8.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)C(=Cc1ccc(OCc2ccc3ccccc3n2)cc1)c1ccncc1
Reaction #62200
4-(4-((quinolin-2-yl)methoxy)phenyl)-3-(pyridin-4-yl)but-3-en-2-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1n[nH]c(-c2ccc(OCc3ccc4ccccc4n3)cc2)c1-c1ccncc1
Reaction #62201
2-((4-(3-Methyl-4-(pyridin-4-yl)-1H-pyrazol-5-yl)phenoxy)methyl)quinoline
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)/C=C/c1ccc2c(c1)c(C#N)cn2-c1ccc(C(=O)O)cc1
Reaction #160543
title compound
Ausbeute 35.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1cc2cc(O)ccc2c(Oc2ccc(C=CC(=O)O)cc2)c1-c1ccccc1
Reaction #173169
DOI: 10.1039/C8SC04228D
CCOC(=O)C(=Cc1ccccc1Br)P(=O)(OCC)OCC
Reaction #175442
DOI: 10.1039/C8SC04228D
CCOCCN(C)c1ccc(-c2ccc3c(c2)C=C(C(=O)O)CCN3C=O)cc1
Reaction #179445
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2cccc(C=CC(=O)Nc3ccc(CN4CCCCC4CCO)cc3)c2)cc1
Reaction #185671
DOI: 10.1039/C8SC04228D
CC1CC(C)CN(Cc2ccc(C=CC(=O)Nc3ccc(-c4ccc(Cl)cc4)cc3)cc2)C1
Reaction #185708
DOI: 10.1039/C8SC04228D
CCNC(=O)c1ccc(C=CC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1
Reaction #199292
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2cccc(C=CC(=O)Nc3ccc(CN4CCN(Cc5ccc6c(c5)OCO6)CC4)cc3)c2)cc1
Reaction #201108
DOI: 10.1039/C8SC04228D
COC(=O)CCCCC(=O)CCc1ccccc1OCc1ccc(C2CCCCC2)cc1
Reaction #204030
DOI: 10.1039/C8SC04228D
O=C(O)C=Cc1ccc(Oc2c(-c3ccccc3)c(CCC(F)(F)F)cc3cc(O)ccc23)cc1
Reaction #204656
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2ccc3c(c2)C=C(C(=O)Nc2ccc(C[N+]4(C)CCCCC4)cc2)CCC3)cc1
Reaction #208582
DOI: 10.1039/C8SC04228D
COc1ccc(CCN(C)Cc2ccc(NC(=O)C=Cc3cccc(-c4ccc(C)cc4)c3)cc2)cc1OC
Reaction #210482
DOI: 10.1039/C8SC04228D
CCOP(=O)(CC(CC(C)C)C(=O)NC(CC(C)C)C(=O)NC)CN1C(=O)C(c2ccccc2)=C(c2ccccc2)C1=O
Reaction #212053
DOI: 10.1039/C8SC04228D
COC(=O)C(=Cc1ccc(NC(=O)OC(C)(C)C)c(C)c1COC(C)=O)NC(=O)OCc1ccccc1
Reaction #219337
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](Cc1ccc(NC(=O)OC(C)(C)C)c(C)c1COC(C)=O)NC(=O)OCc1ccccc1
Reaction #219338
Title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(=Cc1ccc(NC(=O)OC(C)(C)C)c(C)c1COC(C)=O)NC(=O)OCc1ccccc1
Reaction #219471
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H](Cc1ccc(NC(=O)OC(C)(C)C)c(C)c1COC(C)=O)NC(=O)OCc1ccccc1
Reaction #219472
Title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
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