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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 #4372

title compound

Выход 98.0%DOI: 10.6084/m9.figshare.5104873.v1

—

Reaction #54989

DOI: 10.6084/m9.figshare.5104873.v1

CCCC(=NOCC)C1=C(OS(=O)(=O)c2ccc(C)cc2)CC(c2c(C)cc(C)c(C(C)=O)c2C)CC1=O

Reaction #64055

5-(3-acetyl-2,4,6-trimethylphenyl)-2-[1-(ethoxyimino)butyl]-3-(4-toluenesulfonyl)oxy-cyclohex-2-en-1-one

Выход 95.6%DOI: 10.6084/m9.figshare.5104873.v1

CCCC(=NOCC)C1=C(O)CC(c2c(C)c(C)c(O)c(C)c2C)CC1=O

Reaction #64063

2-[1-(ethoxyimino)butyl]-3-hydroxy-5-(4-hydroxy-2,3,5,6-tetramethylphenyl)cyclohex-2-en-1-one

Выход 30.3%DOI: 10.6084/m9.figshare.5104873.v1

O=C(Cn1nc(C(F)F)cc1C(F)F)N1CCC(c2nc(C3=NOC(c4c(O)cccc4Cl)C3)cs2)CC1

Reaction #67017

2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-(4-{4-[5-(2-chloro-6-hydroxyphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}piperidin-1-yl)ethanone

DOI: 10.6084/m9.figshare.5104873.v1

C=CCOc1cccc(Cl)c1C1CC(c2csc(C3CCN(C(=O)Cn4nc(C(F)F)cc4C(F)F)CC3)n2)=NO1

Reaction #67018

1-[4-(4-{5-[2-(allyloxy)-6-chlorophenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]-2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]ethanone

Выход 62.3%DOI: 10.6084/m9.figshare.5104873.v1

Reaction #67019

2-[3,5-bis(difluoromethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-chloro-6-(prop-2-yn-1-yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanone

Выход 54.0%DOI: 10.6084/m9.figshare.5104873.v1

C[C@]12CCC(=NOC3CCNCC3)CC1C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12.Cl

Reaction #70351

title compound

DOI: 10.6084/m9.figshare.5104873.v1

C[C@]12CCC(=NOC3CCNC3)CC1C(=O)C[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12.Cl

Reaction #70352

title compound

DOI: 10.6084/m9.figshare.5104873.v1

C[C@H]1C[C@@H]2[C@H](CC[C@]3(C)C(=O)CC[C@@H]23)[C@@]2(C)CCC(=NO[C@@H]3CCNC3)CC12.Cl

Reaction #70353

title compound

Выход 70.0%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

Выход 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

Выход 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

Выход 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

Выход 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

Выход 80.0%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

Выход 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

Выход 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

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

O=C(NN1CCCN(CC(F)(F)F)C1=O)c1ccc(C2=NOC(c3cc(C(F)(F)F)cc(C(F)(F)F)c3)(C(F)(F)F)C2)cc1C(F)(F)F

Reaction #92117

4-[5-[3,5-bis(trifluoromethyl)phenyl]-5-(trifluoromethyl)-4,5-dihydro-1,2-oxazol-3-yl]-N-[2-oxo-3-(2,2,2-trifluoroethyl)-1,3-diazinan-1-yl]-2-(trifluoromethyl)benzamide

DOI: 10.6084/m9.figshare.5104873.v1

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