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797481

C[Si](C)(C)CCOCn1ccnc1CN(Cc1nccn1COCC[Si](C)(C)C)C(=O)c1ccc(C=O)cc1
Reaction #155830
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(C(=O)N(Cc2ncc[nH]2)Cc2ncc[nH]2)cc1
Reaction #155831
title compound
Ausbeute 99.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1ccnc1CN(Cc1ccc(C=O)cc1)Cc1nccn1C
Reaction #293242
DOI: 10.1039/C8SC04228D
Cn1ccnc1CN(Cc1ccc(C(=O)O)cc1)Cc1nccn1C
Reaction #435818
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)CCCCNC(=O)c1ccc(CN(Cc2nccn2C)Cc2nccn2C)cc1
Reaction #435819
4-{[bis(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-N-(4-dipropylaminobutyl)-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)Cc1ccc(NC(=O)c2ccc(CN(Cc3nccn3C)Cc3nccn3C(=O)OCC)cc2)cc1
Reaction #435847
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)Cc1ccc(NC(=O)c2ccc(CN(Cc3nccn3C)Cc3nccn3C(=O)N(C)C)cc2)cc1
Reaction #435863
compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCOC(=O)n1ccnc1CN(Cc1ccc(C(=O)Nc2ccc(CN(CCC)CCC)cc2)cc1)Cc1nccn1C(=O)OCCCCCC
Reaction #435878
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCOC(=O)n1ccnc1CN(Cc1ccc(C(=O)Nc2ccc(CN(CCC)CCC)cc2)cc1)Cc1nccn1C(=O)OCCCCCCC
Reaction #435879
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)n1ccnc1CN(Cc1ccc(C(=O)Nc2ccc(CN(CCC)CCC)cc2)cc1)Cc1nccn1C(=O)OCCCC
Reaction #435880
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)CCCCNC(=O)c1ccc(CN(Cc2nccn2C)Cc2nccn2C)cc1
Reaction #767096
DOI: 10.1039/C8SC04228D
CCCN(CCC)CCCCNCc1ccc(CN(Cc2nccn2C)Cc2nccn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #886709
DOI: 10.1039/C8SC04228D
CCCN(CCC)Cc1ccc(NC(=O)c2ccc(CN(Cc3nccn3C)Cc3nccn3C(=O)N(C)C)cc2)cc1
Reaction #1042960
DOI: 10.1039/C8SC04228D
Cn1ccnc1CN(Cc1ccc(C(=O)O)cc1)Cc1nccn1C
Reaction #1261070
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)CCCCNC(=O)c1ccc(CN(Cc2nccn2C)Cc2nccn2C)cc1
Reaction #1261071
4-{[bis(1-methyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-N-(4-dipropylaminobutyl)-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)Cc1ccc(NC(=O)c2ccc(CN(Cc3nccn3C)Cc3nccn3C(=O)OCC)cc2)cc1
Reaction #1261099
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCN(CCC)Cc1ccc(NC(=O)c2ccc(CN(Cc3nccn3C)Cc3nccn3C(=O)N(C)C)cc2)cc1
Reaction #1261115
compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCOC(=O)n1ccnc1CN(Cc1ccc(C(=O)Nc2ccc(CN(CCC)CCC)cc2)cc1)Cc1nccn1C(=O)OCCCCCC
Reaction #1261130
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCOC(=O)n1ccnc1CN(Cc1ccc(C(=O)Nc2ccc(CN(CCC)CCC)cc2)cc1)Cc1nccn1C(=O)OCCCCCCC
Reaction #1261131
compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)n1ccnc1CN(Cc1ccc(C(=O)Nc2ccc(CN(CCC)CCC)cc2)cc1)Cc1nccn1C(=O)OCCCC
Reaction #1261132
compound
DOI: 10.6084/m9.figshare.5104873.v1
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