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C(CCCO)CCN

OCCCCCCN1CCCc2cc(C=CC=Cc3ccc(-c4nc5ccccc5o4)cc3)ccc21
Reaction #6308
1-(N-hydroxyhexyl-1,2,3,4-tetrahydroquinolin-6-yl)-4-(4-benzoxazol-ylphenyl)-1,3-butadiene
DOI: 10.6084/m9.figshare.5104873.v1
CC(c1cccc(OC(F)(F)F)c1)C1(O)CCCCC1N1CC[C@H](N)C1.Cl.Cl
Reaction #57102
2-[(3S)-3-aminopyrrolidin-1-yl]-1-[3-(trifluoromethoxy)phenyl]ethylcyclohexanol Dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Reaction #58597
base
Ausbeute 98.6%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #58606
solid
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #74737
hydrochloride salt
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1(O)CN2CCC1CC2
Reaction #76781
tan crystalline subtitle compound
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1
Reaction #77542
solid
Ausbeute 48.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CC1(O)CN2CCC1CC2
Reaction #77878
tan crystalline subtitle compound
Ausbeute 48.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N1C2=CC=CCC2CCC1CO[Si](C)(C)C
Reaction #80765
N-ethoxalyl-2-trimethylsilyloxymethyltetrahydroquinoline
Ausbeute 106.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(=O)N1C2=CC=CCC2CCC1C=O
Reaction #80766
N-ethoxalyl-2-formyltetrahydroquinoline
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1CC(=O)CCN1[C@@H](C)c1ccccc1
Reaction #89424
title compound
Ausbeute 99.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)[C@H]1CC[C@@H](OS(C)(=O)=O)[C@H](NS(=O)(=O)NC(=O)OCc2ccccc2)C1
Reaction #92323
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
O[C@]12CCCC[C@@H]1CCC[C@H]2Nc1ccccc1
Reaction #160791
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O[C@]12CCCC[C@@H]1NCCC2Nc1ccccc1
Reaction #160796
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(=O)N1CCC(Nc2ccccc2)[C@@]2(O)CCCC[C@H]12
Reaction #160797
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCCOc1cc(OCCCCCCCCCC)cc(OCCCCCC(=O)N(Cc2ccc(C(=O)OC)cc2)c2ccc(C(=O)OC)cc2)c1
Reaction #188594
DOI: 10.1039/C8SC04228D
Fc1ccc(OCC2CCC3CN(c4ccc(Cl)nn4)CCN3C2)cc1
Reaction #197725
DOI: 10.1039/C8SC04228D
O=c1c(NCCCCCCOc2ccc(C(F)(F)F)cc2)c(Nc2ccncc2)c1=O
Reaction #198645
DOI: 10.1039/C8SC04228D
CC(=O)c1ccccc1OC(CCCCCN1CCC(c2cccc(NC(=O)C(C)C)c2)CC1)c1ccccc1F
Reaction #200215
DOI: 10.1039/C8SC04228D
CCc1c(CCNC(=O)CCCCC(=O)O)ccc(OC)c1OC
Reaction #200940
DOI: 10.1039/C8SC04228D
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