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1217997

CCNC(=O)N1CCCC12CCN(c1ccc(C(=O)Nc3cc(-c4cccs4)ccc3N)cn1)CC2
Reaction #1260338
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCCNc1ccc(C(=O)Nc2ccccc2N)cn1
Reaction #1782255
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1[nH]c(C=NN=C2C(=O)Nc3ccc(F)cc32)c(C)c1C(=O)NCCCCCCNc1ccc(C(=O)Nc2ccccc2N)cn1
Reaction #1782256
title compound
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC2(CCCN(c3ccc(C(=O)Nc4cc(-c5cccs5)ccc4N)cn3)C2)C1
Reaction #1889735
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2ccccc2)cc1NC(=O)c1ccc(N2CCC3(CC2)CC(C(=O)NCCc2ccccc2)=NO3)nc1
Reaction #1889736
N-(2-phenylethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N1CCCC12CCN(c1ccc(C(=O)Nc3cc(-c4cccs4)ccc3N)cn1)CC2
Reaction #1889737
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC2(CCCN(c3ccc(C(=O)Nc4cc(-c5cccs5)ccc4N)cn3)C2)C1
Reaction #2071957
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2ccccc2)cc1NC(=O)c1ccc(N2CCC3(CC2)CC(C(=O)NCCc2ccccc2)=NO3)nc1
Reaction #2071958
N-(2-phenylethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N1CCCC12CCN(c1ccc(C(=O)Nc3cc(-c4cccs4)ccc3N)cn1)CC2
Reaction #2071959
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NCCCCCCNc1ccc(C(=O)Nc2ccccc2N)cn1
Reaction #2231369
DOI: 10.1039/C8SC04228D
CC(=O)N1CCC2(CCCN(c3ccc(C(=O)Nc4cc(-c5cccs5)ccc4N)cn3)C2)C1
Reaction #2447731
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2ccccc2)cc1NC(=O)c1ccc(N2CCC3(CC2)CC(C(=O)NCCc2ccccc2)=NO3)nc1
Reaction #2447732
N-(2-phenylethyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)N1CCCC12CCN(c1ccc(C(=O)Nc3cc(-c4cccs4)ccc3N)cn1)CC2
Reaction #2447733
title compound
DOI: 10.6084/m9.figshare.5104873.v1