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29791

c1ccc2c(c1)-c1ccccc1C2N1CCNCC1
Reaction #64893
title compound
Ausbeute 81.1%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(Cl)ccc1NC(=O)COCC(=O)N1CCN(C2c3ccccc3-c3ccccc32)CC1
Reaction #235652
DOI: 10.1039/C8SC04228D
O=CN1CCN(C2c3ccccc3-c3ccccc32)CC1
Reaction #377328
DOI: 10.1039/C8SC04228D
c1ccc2c(c1)-c1ccccc1C2N1CCNCC1
Reaction #771999
DOI: 10.1039/C8SC04228D
O=C(c1ccc2[nH]ccc2c1)N1CCN(C2c3ccccc3-c3ccccc32)CC1
Reaction #900322
DOI: 10.1039/C8SC04228D
O=C(c1ccc2[nH]ccc2c1)N1CCN(C2c3ccccc3-c3ccccc32)CC1
Reaction #929211
[4-(9H-Fluoren-9-yl)-piperazin-1-yl]-(1H-indol-5-yl)-methanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)C[C@H](NC(=O)N1CCCCCC1)C(=O)N1CCN(C2c3ccccc3-c3ccccc32)CC1
Reaction #1077555
pure titled compound
Ausbeute 37.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCN(C2c3ccccc3-c3ccccc32)CC1)n1nnc2ncccc21
Reaction #1234040
DOI: 10.1039/C8SC04228D