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CCC(=O)CC

CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(OCc4cccc(CO[Si](C)(C)C(C)(C)C)c4)C(OC)C3)C(C)C(O[Si](C)(C)C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #6392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(O)C(OC)C3)C(C)C(O[Si](C)(C)C(C)(C)C)CC1=O)C(C)CC2OC
Reaction #6398
title compound
Ausbeute 58.4%DOI: 10.6084/m9.figshare.5104873.v1
C=CCOC1CCC(C=C(C)C2OC(=O)C3CCCCN3C(=O)C(=O)C3(O)OC(C(OC)CC(C)CC(C)=CC(CC)C(=O)CC(O[Si](C)(C)C(C)(C)C)C2C)C(OC)CC3C)CC1OC
Reaction #6399
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC1C=C(C)CC(C)CC(OC)C2OC(O)(C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)=CC3CCC(Oc4cccc(C=O)c4)C(OC)C3)C(C)C(O)CC1=O)C(C)CC2OC
Reaction #6401
title compound
Ausbeute 31.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](N=[N+]=[N-])C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40601
38
Ausbeute 87.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](N)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40602
39
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](NC(C)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40603
40
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](OC(=O)C(C)C)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40604
10
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](NS(C)(=O)=O)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40605
42
Ausbeute 575.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@@H]1C[C@H](NS(=O)(=O)c2ccccc2)C(=O)[C@H]2[C@@]1(C)CC[C@H]1C(=O)O[C@H](c3ccoc3)C[C@]21C
Reaction #40606
43
Ausbeute 98.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCSCc1c(C)cc(C)c(C2CC(=O)C(C(CCC)=NOCC)=C(O)C2)c1C
Reaction #64059
5-[3-(n-Butylthiomethyl)-2,4,6-trimethylphenyl]-2-[1-(ethoxyimino)butyl]-3-hydroxycyclohex-2-en-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)C1=C(O)CC(c2c(C)cc(O)cc2C)CC1=O
Reaction #64060
5-(2,6-dimethyl-4-hydroxyphenyl)-3-hydroxy-2-propionylcyclohex-2-en-1-one
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(=O)C(c2cccc(F)c2F)N(c2ccc3[nH]cnc3c2)C1=O
Reaction #70028
Ethyl 1-(1H-benzo[d]imidazol-5-yl)-2,4-dioxo-5-(2,3-difluorophenyl)pyrrolidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1C(=O)C(c2cc(F)cc(F)c2F)N(c2ccc3[nH]cnc3c2)C1=O
Reaction #70029
Ethyl 1-(1H-benzo[d]imidazol-5-yl)-2,4-dioxo-5-(2,3,5-trifluorophenyl)pyrrolidine-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(c2ccc(C3C(=O)CC(=O)N3c3ccc4[nH]cnc4c3)cc2)CC1
Reaction #70040
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-(4-methylpiperazin-1-yl)phenyl)-pyrrolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N(c2ccc3[nH]cnc3c2)C1c1ccc(N2CCC(O)CC2)cc1
Reaction #70042
1-(1H-Benzo[d]imidazol-5-yl)-5-(4-(4-hydroxypiperidin-1-yl)phenyl)-pyrrolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N(c2ccc3[nH]cnc3c2)C1c1cccc(F)c1F
Reaction #70044
1-(1H-Benzo[d]imidazol-5-yl)-5-(2,3-difluorophenyl)pyrrolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CC(=O)N(c2ccc3[nH]cnc3c2)C1c1cc(F)cc(F)c1F
Reaction #70045
1-(1H-Benzo[d]imidazol-5-yl)-5-(2,3,5-trifluorophenyl)pyrrolidine-2,4-dione
DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CC[C@H]3[C@@H](C[C@@H]4O[C@@]45C[C@@H](O)CC[C@]35C)[C@@H]1CCC2=O
Reaction #70359
3β-hydroxy-5α,6α-epoxyandrostane-17-one
Ausbeute 47115.7%DOI: 10.6084/m9.figshare.5104873.v1
C[C@]12CCC(=O)CC1[C@@H](C(N)=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12
Reaction #70368
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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