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1337085

O=C(Cl)C=Cc1cccc([N+](=O)[O-])c1
Reaction #95085
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #95086
title product
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C=Cc1cccc([N+](=O)[O-])c1
Reaction #396532
DOI: 10.1039/C8SC04228D
O=C(Cl)C=Cc1cccc([N+](=O)[O-])c1
Reaction #467904
3-nitrocinnamoyl chloride
Ausbeute 96.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C=Cc1cccc([N+](=O)[O-])c1
Reaction #935683
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #935684
title product
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #935748
title product
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C=Cc1cccc([N+](=O)[O-])c1
Reaction #1152999
title compound
Ausbeute 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #1153000
title product
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C=Cc1cccc([N+](=O)[O-])c1
Reaction #1574301
3-nitro cinnamoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCCC(C)NC(=O)C=Cc1cccc([N+](=O)[O-])c1
Reaction #1661381
DOI: 10.1039/C8SC04228D
O=C(Cl)C=Cc1cccc([N+](=O)[O-])c1
Reaction #2207500
3-nitrocinnamoyl chloride
Ausbeute 96.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(C=Cc1cccc([N+](=O)[O-])c1)Oc1cccc([N+](=O)[O-])c1
Reaction #2207501
light yellow colored needle-like
Ausbeute 90.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)C=Cc1cccc([N+](=O)[O-])c1
Reaction #2219494
DOI: 10.1039/C8SC04228D
O=C(C=Cc1cccc([N+](=O)[O-])c1)Oc1cccc([N+](=O)[O-])c1
Reaction #2234328
DOI: 10.1039/C8SC04228D
CCCCCN1C(=O)C(C)(C)c2cc3[nH]c(/C=C/c4cccc(N)c4)nc3cc21
Reaction #2322589
2-[(E)-2-(3-Amino-phenyl)-vinyl]-7,7-dimethyl-5-pentyl-5,7-dihydro-1H-imidazo[4,5-f]indol-6-one
Ausbeute 52.9%DOI: 10.6084/m9.figshare.5104873.v1