Teilstruktursuche

24786

O=C(c1ccc([N+](=O)[O-])c(OCc2ccc(-c3ccccc3-c3nnnn3C(c3ccccc3)(c3ccccc3)c3ccccc3)cc2)c1)N1CCOCC1
Reaction #2824
compound
Ausbeute 101.9%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C1c2c(ncn2Cc2ccc(-c3ccccc3-c3nnnn3C(c3ccccc3)(c3ccccc3)c3ccccc3)cc2)CCN1C(=O)C(c1ccccc1)c1ccccc1
Reaction #50131
methyl 5-diphenylacetyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate
Ausbeute 11.8%DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #64450
white crystals
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc([N+](=O)[O-])c1N(Cc1ccc(-c2ccccc2-c2nnnn2Cc2ccc(OC)cc2)cc1)C(=O)OC(C)(C)C
Reaction #70073
methyl 2-(N-tert-butoxycarbonyl-N-{(2′-[1-(p-methoxybenzyl)-1H-tetrazol-5-yl]biphenyl-4-yl)methyl}amino)-3-nitrobenzoate
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cccc([N+](=O)[O-])c1N(Cc1ccc(-c2ccccc2-c2nnnn2Cc2ccccc2)cc1)C(=O)OC(C)(C)C
Reaction #70076
methyl 2-(N-tert-butoxycarbonyl-N-{(2′-[1-benzyl-1H-tetrazol-5-yl]biphenyl-4-yl)methyl}amino)-3-nitrobenzoate
Ausbeute 81.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81170
title compound
Ausbeute 79.9%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C(O)(CC)CC)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81172
title compound
Ausbeute 52.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C(C)(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81174
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C(C)(O)CC)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81175
title compound
Ausbeute 72.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(O)CC)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81178
title compound
Ausbeute 77.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(=O)OCC)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81182
title compound
Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C(=O)OC)c(C(=O)OC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81188
title compound
Ausbeute 34.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)O)c(C(=O)OCC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81193
title compound
Ausbeute 72.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCc2oc(=O)oc2C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81233
title compound
Ausbeute 49.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OCOC(=O)C(C)(C)C)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81235
title compound
Ausbeute 48.8%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(C)(C)O)c(C(=O)OC2OC(=O)c3ccccc32)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81236
title compound
Ausbeute 18.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(C(C)(C)O)nc(CC)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81240
title compound
Ausbeute 64.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(=O)C(C)(C)C)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81246
title compound
Ausbeute 85.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1nc(C(=O)C(C)(C)C)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81250
title compound
Ausbeute 87.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1nc(C(=O)C(C)C)c(C#N)n1Cc1ccc(-c2ccccc2-c2nnnn2C(c2ccccc2)(c2ccccc2)c2ccccc2)cc1
Reaction #81254
title compound
Ausbeute 59.0%DOI: 10.6084/m9.figshare.5104873.v1
Seite 1Weiter