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1216835

COc1ccc(/C=C(/C#N)c2cc(OC)c(OC)c(OC)c2)cc1[N+](=O)[O-]

intended compound

Ausbeute 49.8%DOI: 10.6084/m9.figshare.5104873.v1

COc1ccc(/C=C(/C#N)c2cc(OC)c(OC)c(OC)c2)cc1N

intended compound

Ausbeute 99.5%DOI: 10.6084/m9.figshare.5104873.v1

COc1cc(/C(C#N)=C/c2ccc(C)c([N+](=O)[O-])c2)cc(OC)c1OC

intended compound

Ausbeute 14.1%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C(C#N)=C\c2ccc(C)c([N+](=O)[O-])c2)cc(OC)c1OC$

intended compound

Ausbeute 7.2%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C(C#N)=C\c2ccc(C)c(N)c2)cc(OC)c1OC$

intended compound

Ausbeute 78.0%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C(C#N)=C\c2ccc(Cl)c([N+](=O)[O-])c2)cc(OC)c1OC$

intended compound

Ausbeute 26.7%DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C(C#N)=C\c2ccc(Cl)c(N)c2)cc(OC)c1OC$

desired product

Ausbeute 33.6%DOI: 10.6084/m9.figshare.5104873.v1

C[Si](C)(C)CCOCn1ccc2c(-c3cnn(C(CC#N)c4cccc([N+](=O)[O-])c4)c3)ncnc21

Reaction #69225

3-(3-nitrophenyl)-3-[4-(7-[2-(trimethylsilyl)ethoxy]methyl-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]propanenitrile

DOI: 10.6084/m9.figshare.5104873.v1

$COc1cc(/C=C(\C#N)c2ccc(C(F)(F)F)nc2)cc([N+](=O)[O-])c1O$

Reaction #70926

(Z)-3-(4-hydroxy-3-methoxy-5-nitrophenyl)-2-(6-(trifluoromethyl)pyridin-3-yl)acrylonitrile

DOI: 10.6084/m9.figshare.5104873.v1

$N#C/C(=C\c1cc(O)c(O)c([N+](=O)[O-])c1)c1ccc(C(F)(F)F)nc1$

Reaction #70927

(Z)-3-(3,4-dihydroxy-5-nitrophenyl)-2-(6-(trifluoromethyl)pyridin-3-yl)acrylonitrile

DOI: 10.6084/m9.figshare.5104873.v1

$N#C/C(=C\c1cc(O)c(O)c([N+](=O)[O-])c1)c1ccc(C(F)(F)F)nc1$

Reaction #90272

(Z)-3-(3,4-dihydroxy-5-nitrophenyl)-2-(6-(trifluoromethyl)pyridin-3-yl)acrylonitrile

DOI: 10.6084/m9.figshare.5104873.v1

CN(C)C(=O)C(C#N)=Cc1cc(O)c(O)c([N+](=O)[O-])c1

Reaction #178868

DOI: 10.1039/C8SC04228D

N#CC=Cc1cccc(NC(=O)c2ccc(-c3ccccc3)o2)c1

Reaction #181737

DOI: 10.1039/C8SC04228D

Cc1ccc([N+](=O)[O-])cc1C=CC#N

Reaction #192920

DOI: 10.1039/C8SC04228D

CCOP(=O)(OCC)C(C#N)=Cc1cc(-n2c(=O)cc(C(F)(F)F)n(C)c2=O)c(F)cc1Cl

Reaction #193066

DOI: 10.1039/C8SC04228D

CC(C)NC(=O)C(C#N)=Cc1cc(O)c(O)c([N+](=O)[O-])c1

Reaction #210784

DOI: 10.1039/C8SC04228D

CCOc1cc(C=C(C#N)C(=O)N(CC)CC)cc([N+](=O)[O-])c1O

Reaction #219199

N,N-diethyl-2-cyano-3-(-3-ethoxy-4-hydroxy-5-nitrophenyl)acrylamide

Ausbeute 172.7%DOI: 10.6084/m9.figshare.5104873.v1

CCN(CC)C(=O)C(C#N)=Cc1cc(OC)c(O)c([N+](=O)[O-])c1

Reaction #219200

N,N-diethyl-2-cyano-3-(3-methoxy-4-hydroxy-5-nitrophenyl)acrylamide

Ausbeute 162.0%DOI: 10.6084/m9.figshare.5104873.v1

COc1ccc(C=C(C#N)c2cc(OC)c(OC)c(OC)c2)cc1N

Reaction #225310

DOI: 10.1039/C8SC04228D

CCOC(=O)C(C#N)=Cc1cc([N+](=O)[O-])ccc1Cl

Reaction #241455

DOI: 10.1039/C8SC04228D

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