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1417174

O=[N+]([O-])c1ccc(C#CCO)cc1
Reaction #53209
4-(3-hydroxyprop-1-ynyl)-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(S(=O)(=O)OCC#Cc2ccc([N+](=O)[O-])cc2)cc1
Reaction #53210
4-[3-(p-Tolylsulphonyloxy)-prop-1-ynyl]-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)CC#Cc1ccc([N+](=O)[O-])cc1
Reaction #53211
4-(3-dimethylaminoprop-1-ynyl)-nitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(C#CCO)ccc1[N+](=O)[O-]
Reaction #339995
compound 72
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NCc2ccc(C(=O)Nc3cc(C#CCO)ccc3[N+](=O)[O-])cc2)cc1OC
Reaction #339996
4-[(3,4-Dimethoxy-phenylamino)-methyl]-N-[5-(3-hydroxy-prop-1-ynyl)-2-nitro-phenyl]-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C#Cc1ccc([N+](=O)[O-])cc1
Reaction #404248
DOI: 10.1039/C8SC04228D
COc1cc(C#CCO)ccc1[N+](=O)[O-]
Reaction #506660
title compound
Ausbeute 47.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C#CCCl)ccc1[N+](=O)[O-]
Reaction #506661
title compound
Ausbeute 97.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(NCc2ccc(C(=O)Nc3cc(C#CCO)ccc3[N+](=O)[O-])cc2)cc1OC
Reaction #782655
DOI: 10.1039/C8SC04228D
CCOC(=O)C#Cc1ccc([N+](=O)[O-])cc1
Reaction #899122
DOI: 10.1039/C8SC04228D
O=[N+]([O-])c1ccc(CCCO)c(Cl)c1
Reaction #985735
3-(2-chloro-4-nitro-phenyl)-propan-1-ol
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCOc1ccc(NC(=O)C#Cc2ccc([N+](=O)[O-])cc2Cl)cc1Cl
Reaction #1028945
DOI: 10.1039/C8SC04228D
COc1cc(C#CCO)ccc1[N+](=O)[O-]
Reaction #1032299
DOI: 10.1039/C8SC04228D
CC1CCN(c2cc(C#CCO)ccc2[N+](=O)[O-])CC1
Reaction #1277369
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C)CC#Cc1ccc([N+](=O)[O-])c(N2CCC(C)CC2)c1
Reaction #1277370
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C#Cc1ccc([N+](=O)[O-])cc1
Reaction #1340982
compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(OC(=O)C#Cc2ccc([N+](=O)[O-])cc2)cc(C)c1Br
Reaction #1570372
title compound 7-1
Ausbeute 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1CCN(c2cc(C#CCO)ccc2[N+](=O)[O-])CC1
Reaction #1595304
title compound
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C)CC#Cc1ccc([N+](=O)[O-])c(N2CCC(C)CC2)c1
Reaction #1595305
title compound
Ausbeute 100.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C#CCCl)ccc1[N+](=O)[O-]
Reaction #1647979
DOI: 10.1039/C8SC04228D
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