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580669

COC(=O)C(Cc1ccc2ccccc2c1)N1CCN(S(=O)(=O)c2ccccc2[N+](=O)[O-])C(CCCNC(=O)OCc2ccccc2)C1=O
Reaction #8624
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C(Cc1ccc2ccccc2c1)N1CCNC(CCO[Si](C)(C)C(C)(C)C)C1=O
Reaction #8626
desired product
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN([C@H](C(=O)N1CC[C@H](O[Si](C)(C)C(C)(C)C)C1)c1ccccc1)S(=O)(=O)c1ccccc1[N+](=O)[O-]
Reaction #51863
N-Allyl-N-{2-[3-(S)-(tert-butyl-dimethyl-silanyloxy)-pyrrolidin-1-yl]-2-oxo-1-(S)-phenyl-ethyl}-2-nitro-benzenesulfonamide
DOI: 10.6084/m9.figshare.5104873.v1
C=CCN[C@H](C(=O)N1CC[C@H](O[Si](C)(C)C(C)(C)C)C1)c1ccccc1
Reaction #51864
title compound
Ausbeute 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCN(CCNc1ccc([N+](=O)[O-])cn1)S(=O)(=O)c1ccccc1[N+](=O)[O-]
Reaction #60211
[2-(dimethylamino)ethyl]{2-[(5-nitro(2-pyridyl))amino]ethyl}[(2-nitrophenyl)sulfonyl]amine
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CCNCCNc1ccc([N+](=O)[O-])cn1
Reaction #60212
dimethyl[2-({2-[(5-nitro(2-pyridyl))amino]-ethyl}amino)ethyl]amine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(NCCN(CCN2CCCC2)S(=O)(=O)c2ccccc2[N+](=O)[O-])nc1
Reaction #60213
{2-[(5-nitro(2-pyridyl))amino]ethyl}[(2-nitrophenyl)sulfonyl](2-pyrrolidinylethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(NCCN(CCN2CCOCC2)S(=O)(=O)c2ccccc2[N+](=O)[O-])nc1
Reaction #60214
(2-morpholin-4-ylethyl){2-[(5-nitro(2-pyridyl))amino]ethyl}[(2-nitrophenyl)sulfonyl]amine
DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(CCCN(CCn3ccc4ccccc4c3=O)S(=O)(=O)c3ccccc3[N+](=O)[O-])ccc21
Reaction #156169
title compound
Ausbeute 26.5%DOI: 10.6084/m9.figshare.5104873.v1
CCN1C(=O)C(C)(C)C(=O)N(C)c2cc(CCCNCCn3ccc4ccccc4c3=O)ccc21
Reaction #156170
title compound
Ausbeute 68.3%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)ccc2cc(OCCCCCN(CCc3cccnc3)S(=O)(=O)c3ccccc3[N+](=O)[O-])ccc21
Reaction #156184
title compound
Ausbeute 96.9%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(=O)ccc2cc(OCCCN(CCN3CCC(OCc4cccnc4)CC3)S(=O)(=O)c3ccccc3[N+](=O)[O-])ccc21
Reaction #156200
title compound
Ausbeute 67.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(C)c3c(-c4nc5c(c(N6CCN(S(=O)(=O)c7ccccc7[N+](=O)[O-])[C@H](C)C6)n4)CN(Cc4ccccc4)CC5)cccc32)cc1
Reaction #167990
(R)-6-benzyl-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methyl-4-((2-nitrophenyl)sulfonyl)piperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(C)c3c(-c4nc5c(c(N6CCN(S(=O)(=O)c7ccccc7[N+](=O)[O-])[C@H](C)C6)n4)CNCC5)cccc32)cc1
Reaction #167991
(R)-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methyl-4-((2-nitrophenyl)sulfonyl)piperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)n2cc(C)c3c(-c4nc5c(c(N6CCN[C@H](C)C6)n4)CN(c4cc(C(C)C)nn4C)CC5)cccc32)cc1
Reaction #167992
(R)-6-(3-isopropyl-1-methyl-1H-pyrazol-5-yl)-2-(3-methyl-1-tosyl-1H-indol-4-yl)-4-(3-methylpiperazin-1-yl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
COCCN(CCN1CCS(=O)(=O)CC1)S(=O)(=O)c1ccccc1[N+](=O)[O-]
Reaction #172745
title compound
Ausbeute 105.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCNCCN1CCS(=O)(=O)CC1
Reaction #172746
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCCN(CCN1CCS(=O)(=O)CC1)S(=O)(=O)c1ccccc1[N+](=O)[O-]
Reaction #172747
title compound
Ausbeute 109.0%DOI: 10.6084/m9.figshare.5104873.v1
COCCCNCCN1CCS(=O)(=O)CC1
Reaction #172748
oil
Ausbeute 87.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccccc1S(=O)(=O)N(CCN1CCS(=O)(=O)CC1)CCN1CCS(=O)(=O)CC1
Reaction #172749
title compound
Ausbeute 119.2%DOI: 10.6084/m9.figshare.5104873.v1
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