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1224640

C=CC[C@@]1(O)OCCN(Cc2ccccc2)[C@H]1c1ccc(F)cc1
Reaction #2156
(2R,3S)-4-Benzyl-3-(4-fluorophenyl)-2-hydroxy-2-(prop-2-enyl)morpholine
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCN1CCC(c2ccc(F)nc2)CC1)C(=O)C(c1ccc(F)cc1)c1ccc(F)cc1
Reaction #40582
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](O)[C@H](NC(=O)OC(C)(C)C)c1cc(F)c(F)c(F)c1
Reaction #44601
title compound
Ausbeute 86.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H](N)c1cc(F)c(F)c(F)c1.Cl
Reaction #44604
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(/C=C2\CCCN([C@H](c3cc(F)c(F)c(F)c3)[C@@H](C)O)C2=O)ccc1-n1cnc(C)c1
Reaction #44605
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(/C=C2\CC[C@H]3COC[C@@H](c4cc(F)c(F)c(F)c4)N3C2=O)ccc1-n1cnc(C)c1
Reaction #44630
title compound
Ausbeute 38.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](O)[C@H]1COC[C@@H](c2cc(F)c(F)c(F)c2)N1C(=O)OCc1ccccc1
Reaction #44666
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@H]1COC[C@@H](c2cc(F)c(F)c(F)c2)N1C(=O)OCc1ccccc1
Reaction #44667
titled compound
Ausbeute 91.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)[C@H]1COC[C@@H](c2cc(F)c(F)c(F)c2)N1
Reaction #44668
titled compound
Ausbeute 100.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC(COCC1CCNCC1)c1ccc(F)cc1)c1ccc2c(Cl)c[nH]c2c1
Reaction #60691
3-Chloro-N-[1-(4-fluorophenyl)-2-(piperidin-4-ylmethoxy)-ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccc(F)cc2)CC1
Reaction #60714
title compound
Ausbeute 76.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(COCC(NC(=O)c2ccc3c(Cl)c[nH]c3c2)c2ccc(F)cc2)CC1
Reaction #60715
3-Chloro-N-[1-(4-fluorophenyl)-2-(1-methylpiperidin-4-yl-methoxy)ethyl]-1H-indole-6-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@@H]1C(=O)N[C@H](C2Cc3ccccc3C2)C(=O)N1[C@@H](C(=O)NCC(F)(F)F)c1ccc(F)cc1
Reaction #73885
(2R)-2-[(3R,6R)-3-(2,3-dihydro-1H-inden-2-yl)-6-isobutyl-2,5-dioxopiperazin-1-yl]-2-(4-fluorophenyl)-N-(2,2,2-trifluoroethyl)ethanamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC(C)OC(=O)[C@@H](c1ccc(F)cc1F)N1C(=O)[C@@H](C2Cc3ccccc3C2)NC(=O)[C@H]1CC(C)C
Reaction #73899
1-(acetyloxy)ethyl (2R)-(2,4-difluorophenyl)[(3R,6R)-3-(2,3-dihydro-1H-inden-2-yl)-6-isobutyl-2,5-dioxopiperazin-1-yl]ethanoate
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc([C@]23CO[C@H](COC(c4ccccc4)(c4ccccc4)c4ccccc4)[C@H]2CON3)c(F)c1Cl
Reaction #155552
title compound
Ausbeute 34.3%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(c2ccc(F)c(Cl)c2F)CO[C@H](COC(c2ccccc2)(c2ccccc2)c2ccccc2)[C@H]1CO
Reaction #155553
title compound
Ausbeute 96.9%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@]1(c2ccc(F)cc2F)CO[C@H](COC(c2ccccc2)(c2ccccc2)c2ccccc2)[C@H]1CO
Reaction #155554
title compound
Ausbeute 99.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3ccc(F)cc3F)CO[C@H](CO)[C@H]2CS1)c1ccccc1
Reaction #155557
title compound
Ausbeute 89.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3ccc(F)cc3F)CO[C@H](CF)[C@H]2CS1)c1ccccc1
Reaction #155558
title compound
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3ccc(F)cc3F)CO[C@H](CF)[C@H]2CS1
Reaction #155559
title compound
Ausbeute 104.2%DOI: 10.6084/m9.figshare.5104873.v1
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