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15954

CCCCCNCCC12CC3CC(CC(C3)C1)C2.Cl
Reaction #11528
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
CNCCC12CC3CC(CC(C3)C1)C2
Reaction #11530
titled compound
Ausbeute 66.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)CCNCCC12CC3CC(CC(C3)C1)C2.Cl
Reaction #11531
titled compound
Ausbeute 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11558
titled compound
Ausbeute 73.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CCCCc1ccncc1
Reaction #11559
titled compound
Ausbeute 33.0%DOI: 10.6084/m9.figshare.5104873.v1
CNCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1.Cl.Cl
Reaction #11560
titled compound
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)OCCCc1ccncc1
Reaction #11562
titled compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CCN(CCC23CC4CC(CC(C4)C2)C3)C(=O)N1CCCc1ccncc1
Reaction #11563
titled compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=S)NCCCc1ccncc1
Reaction #11564
titled compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N(CCCc2ccncc2)CCCN1CCC12CC3CC(CC(C3)C1)C2
Reaction #11566
titled compound
Ausbeute 9.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)NN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11567
titled compound
Ausbeute 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(CCCc1ccncc1)C(=O)N(C)CCC12CC3CC(CC(C3)C1)C2
Reaction #11568
titled compound
Ausbeute 141.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCCCc1ccncc1)N(O)CCC12CC3CC(CC(C3)C1)C2
Reaction #11569
titled compound
Ausbeute 34.0%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
COCCN(C)CCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCCc1ccncc1
Reaction #11574
titled compound
Ausbeute 32.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)CBr
Reaction #11575
2-bromoacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide
DOI: 10.6084/m9.figshare.5104873.v1
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