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685606

CCOC(=O)C(C#N)=CNc1ccc(CC)cn1
Reaction #193170
DOI: 10.1039/C8SC04228D
CCCCc1ccc(NC=C(C#N)C(=O)OCC)nc1
Reaction #233880
DOI: 10.1039/C8SC04228D
CCCCc1cccnc1NC=C(C#N)C(=O)OCC
Reaction #918218
DOI: 10.1039/C8SC04228D
CCc1ccc2ncc(-c3nnn[nH]3)c(=O)n2c1
Reaction #1199707
title compound
Ausbeute 28.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc2ncc(-c3nnn[nH]3)c(=O)n2c1
Reaction #1199708
title compound
Ausbeute 30.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1cccnc1NC=C(C#N)C(=O)OCC
Reaction #1549163
title compound
Ausbeute 84.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=CNc1ncccc1Cl
Reaction #1549165
title compound
Ausbeute 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(C#N)=CNc1ncccc1Cl
Reaction #1633599
DOI: 10.1039/C8SC04228D
CCOC(=O)C(C#N)=CNc1ccc(CC)cn1
Reaction #1788584
title compound
Ausbeute 25.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCc1ccc(NC=C(C#N)C(=O)OCC)nc1
Reaction #1788585
Ethyl 2-Cyano-3-(5-n-butyl-2-pyridylamino)acrylate
DOI: 10.6084/m9.figshare.5104873.v1