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Cc1ccc(-c2ccccc2)cc1

CCCCCC[C@@H](F)COc1c(F)cc(-c2ccc([C@H]3CC[Si@H](CCC)CC3)cc2)cc1F
Reaction #2740
(R)-4-(4-(trans-4-n-propyl-4-silacyclohexyl)phenyl)-1-(2-fluorooctyloxy)2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCC[Si@H]1CC[C@H](c2ccc(-c3cc(F)c(OC[C@@H](F)CCCCCC)c(F)c3)cc2)CC1
Reaction #2742
(S)-4-(4-(trans-4-n-nonyl-4-silacyclohexyl)phenyl)-1-(2-fluorooctyloxy)-2,6-difluorobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc2cccc(C(=O)OC)c2n1Cc1ccc(-c2ccccc2-c2nc(=S)o[nH]2)cc1
Reaction #5339
prisms
Ausbeute 32.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(-c2ccc3c(c2)C2(CCCCC2)C(=O)N3)cc1F
Reaction #7103
title compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(CN2Cc3cncn3C(c3ccc(-c4ccc(Cl)cc4)cc3)C2=O)cc1
Reaction #43693
5-(4′-chlorobiphenyl-4-yl)-7-(4-methoxy-benzyl)-7,8-dihydro-imidazo[1,5-a]pyrazin-6-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](Oc1ccc(Cl)cc1-c1ccc(C(=O)NC(C)(C)C)c(F)c1)C(=O)O
Reaction #44390
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2O)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52920
N-(2,6-dichlorobenzoyl)-4-(2-hydroxyphenyl)-L-phenylalanine methyl ester
Ausbeute 50.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](Cc1ccc(-c2ccccc2OCC#N)cc1)NC(=O)c1c(Cl)cccc1Cl
Reaction #52922
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(O)c1-c1ccc(C[C@H](NC(=O)c2c(Cl)cccc2Cl)C(=O)O)cc1
Reaction #52974
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ccc(C(=O)Nc3ccc(CN(C)CCN(C)C)cn3)c3nccnc23)c1
Reaction #71400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ccc(C(=O)O)c3nccnc23)c1
Reaction #71401
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN1CCN(Cc2ccc(NC(=O)c3ccc(-c4cc(OC)cc(OC)c4F)c4nccnc34)nc2)CC1
Reaction #71403
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(OC)c(F)c(-c2ccc(C(=O)Nc3nc(CN4CCCC4)c[nH]3)c3nccnc23)c1
Reaction #71404
title compound
DOI: 10.6084/m9.figshare.5104873.v1
[Br-].c1ccc(-c2ccc(CCCCC[n+]3cccc4ccccc43)cc2)cc1
Reaction #171536
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
[Br-].c1ccc(-c2ccc(CCCCC[n+]3ccc4ccccc4c3)cc2)cc1
Reaction #171537
title compound
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(C(=O)O)c1cc(C#N)c(OCC2CC2)c(-c2ccc(C(F)(F)F)cc2)c1
Reaction #173492
DOI: 10.1039/C8SC04228D
CCCCCCCCc1ccc(-c2ccc(COc3ccc(OCC(C)OC(=O)OCCCC)cc3)cc2)cc1
Reaction #175740
DOI: 10.1039/C8SC04228D
CCCN1CCN(CCOc2ccc(OCc3ccccc3)c(C(=O)Nc3cc(-c4ccccc4)ccc3C(=O)OC)c2)CC1
Reaction #176025
DOI: 10.1039/C8SC04228D
C=CC(=O)OCCCCCCOc1ccc(-c2ccc(C3CCC(CCCO)CC3)cc2)cc1
Reaction #183535
DOI: 10.1039/C8SC04228D
O=C(O)CSc1nc2cc(-c3ccc(-c4ccccc4O)cc3)c(Cl)cc2[nH]1
Reaction #189650
DOI: 10.1039/C8SC04228D
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