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CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11558
titled compound
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1cc[n+](C)cc1.[I-]
Reaction #11561
titled compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1.Cl
Reaction #11570
titled compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCC(O)c1ccncc1
Reaction #11571
titled compound
Ausbeute 55.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NC[C@@H]1C[C@@H]1c1ccncc1
Reaction #11572
titled compound
Ausbeute 3.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1cc[n+]([O-])cc1
Reaction #11573
titled compound
Ausbeute 94.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CCNCc1ccncc1
Reaction #11580
titled compound
Ausbeute 36.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCC(=O)c1ccncc1
Reaction #11584
titled compound
Ausbeute 87.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCC(O)c1ccncc1
Reaction #46685
1-[2-(1-Adamantyl)ethyl]-3-[3-hydroxy-3-(4-pyridyl)propyl]-1-pentylurea
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CCNCc1ccncc1
Reaction #46691
compound
Ausbeute 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #224708
DOI: 10.1039/C8SC04228D
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1cc[n+](C)cc1
Reaction #270091
DOI: 10.1039/C8SC04228D
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CCNCc1ccncc1
Reaction #764116
DOI: 10.1039/C8SC04228D
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCC1CC1c1ccncc1
Reaction #789596
DOI: 10.1039/C8SC04228D
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1cc[n+]([O-])cc1
Reaction #899692
DOI: 10.1039/C8SC04228D
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #1480348
titled compound
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1cc[n+](C)cc1.[I-]
Reaction #1480351
titled compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1.Cl
Reaction #1480360
titled compound
Ausbeute 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCC(O)c1ccncc1
Reaction #1480361
titled compound
Ausbeute 55.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NC[C@@H]1C[C@@H]1c1ccncc1
Reaction #1480362
titled compound
Ausbeute 3.5%DOI: 10.6084/m9.figshare.5104873.v1
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