Teilstruktursuche

412189

—
Reaction #58688
free base
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #78932
oil
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1N1CCN(CC2CCCN(C(=O)OC(C)(C)C)C2)CC1
Reaction #78933
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(C(Oc2n[nH]c3ccc(F)cc23)c2ccccc2F)C1
Reaction #203041
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC(COS(C)(=O)=O)C1
Reaction #265141
DOI: 10.1039/C8SC04228D
Cc1onc2c1c(=O)n(C1CC(CN=[N+]=[N-])CN(C(=O)OC(C)(C)C)C1)c1cccc(Cl)c21
Reaction #269104
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCCC(COS(C)(=O)=O)C1
Reaction #273398
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(O)C(CN=[N+]=[N-])C1
Reaction #286501
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC[C@H](COS(C)(=O)=O)C1
Reaction #359277
{(3S)-1-(tert-butoxycarbonyl)-3-piperidyl}methyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H](CN=[N+]=[N-])C1
Reaction #359278
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(COS(C)(=O)=O)C1
Reaction #387316
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1C[C@H](COS(C)(=O)=O)C[C@H](C2CCCCC2)C1
Reaction #470978
tert-butyl cis-3-cyclohexyl-5-{[(methylsulfonyl)oxy]methyl}piperidine-1-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H](COS(C)(=O)=O)C1
Reaction #481229
{(3S)-1-(tert-butoxycarbonyl)-3-piperidyl}methyl methanesulfonate
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@H](CN=[N+]=[N-])C1
Reaction #481230
title compound
Ausbeute 84.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(CI)C1
Reaction #488985
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC(O)C(CN=[N+]=[N-])C1
Reaction #489242
3-azidomethyl-4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@](F)(COS(=O)(=O)C(F)(F)F)C1
Reaction #560496
1,1-dimethylethyl (3S)-3-fluoro-3-({[(trifluoromethyl)sulfonyl]oxy}methyl)-1-piperidinecarboxylate
Ausbeute 106.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@](F)(CN=[N+]=[N-])C1
Reaction #560513
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCCC(COc2cccc(OS(=O)(=O)c3ccccc3Cl)c2)C1
Reaction #569266
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCC[C@@H](COS(C)(=O)=O)C1
Reaction #586403
pale yellow oil
DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter