Recherche de Sous-structure

OCCCCCCC1CCCCC1

CC(=O)O[C@H]1CC[C@H]2[C@@H]3CC[C@H]4CC(=NO)C(=NO)C[C@]4(C)[C@H]3CC[C@]12C

Reaction #928

17β-Acetoxy-2,3-dihydroxyimino-5α-androstane

DOI: 10.6084/m9.figshare.5104873.v1

—

Reaction #70362

solid

Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1

C[C@]12CCC(=O)CC1/C(=N/O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12

Reaction #70370

title compound

Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1

$CO/N=C1\C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=O)CC12$

Reaction #70378

title compound

Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1

$C[C@]12CC[C@H]3[C@@H](C/C(=N\O)[C@@]4(O)CCCC[C@]34C)[C@@H]1CC13OCCOC12OCCO3$

Reaction #70382

17,17-Bis(ethylendioxy)-5α-hydroxy-6-(E)-hydroxyimino-androstane

Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1

$C[C@]12CC[C@H]3[C@@H](C/C(=N\O)[C@@]4(O)CC(=O)CC[C@]34C)[C@@H]1CCC2=O$

Reaction #70383

title compound

Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1

$CO/N=C1\C[C@H]2[C@@H]3CCC(=O)[C@@]3(C)CC[C@@H]2[C@@]2(C)CCC(=O)C[C@]12O$

Reaction #70384

title compound

Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1

$C[C@]12CCCCC1C/C(=N\O)[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1CC13OCCOC12OCCO3$

Reaction #70389

17,17-Bis(ethylendioxy)-7-(E)-hydroxyiminoandrostane

Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1

$C[C@]12CCC(=O)CC1C/C(=N\O)[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12$

Reaction #70390

title compound

Rendement 50.0%DOI: 10.6084/m9.figshare.5104873.v1

$CO/N=C1\CC2CC(=O)CC[C@]2(C)[C@H]2CC[C@]3(C)C(=O)CC[C@H]3[C@H]12$

Reaction #70391

title compound

Rendement 55.0%DOI: 10.6084/m9.figshare.5104873.v1

$C=CCO/N=C1\CC2CC(=O)CC[C@]2(C)[C@H]2CC[C@]3(C)C(=O)CC[C@H]3[C@H]12$

Reaction #70392

title compound

Rendement 76.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #70412

title compound

Rendement 67.0%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #95263

1-acetoxy-2-(5-carbethoxypentyl)cyclohex-1-ene

DOI: 10.6084/m9.figshare.5104873.v1

C[C@H](CC[C@@H](O)C(C)(C)O)[C@H]1CC[C@H]2C3=CC=C4C[C@@H](OC5CCCOC5)CC[C@]4(C)[C@H]3CC[C@]12C

Reaction #95326

(24R)-5,7-cholestadiene-3β,24,25-triol 3-tetrahydropyranyl ether

Rendement 93.0%DOI: 10.6084/m9.figshare.5104873.v1

COC(=O)C1CN(C(=O)c2noc(C(CCCC3CCCCC3)CC(=O)O)n2)C1

Reaction #179860

DOI: 10.1039/C8SC04228D

CCOC(=O)C1COC(C(CCCC2CCCCC2)CC(=O)OC(C)(C)C)=N1

Reaction #181042

DOI: 10.1039/C8SC04228D

COCC(=O)NCc1noc(C(CCCC2CCCCC2)CC(=O)OC(C)(C)C)n1

Reaction #182066

DOI: 10.1039/C8SC04228D

CCC(CC)NCc1noc(C(CCCC2CCCCC2)CC(=O)OC(C)(C)C)n1

Reaction #182392

DOI: 10.1039/C8SC04228D

CCOC(C)OC(C)(C)C(F)CCC(COS(=O)(=O)c1ccc(C)cc1)C1CCC2C3CC=C4CC(OC5CCCCO5)CC(OC5CCCCO5)C4(C)C3CCC12C

Reaction #182809

DOI: 10.1039/C8SC04228D

CCCCC1CCC(C2CCC(C=Cc3cc4ccc(OCC)c(F)c4c(F)c3F)CC2)CC1

Reaction #183042

DOI: 10.1039/C8SC04228D

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