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C=Cc1ccccn1

CCOCc1nc2c(N)nc3cc(/C=C/c4ccccn4)ccc3c2n1CCCOC
Reaction #9599
(E)-2-ethoxymethyl-1-(3-methoxypropyl)-7-(2-pyridin-2-ylvinyl)-1H-imidazo[4,5-c]quinolin-4-amine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C=Cc1ccc2c(n1)N1[C@H](C2)CN(C(=O)OC(C)(C)C)C[C@H]1C
Reaction #12015
desired compound
Ausbeute 91.2%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1CN(C(=O)OC(C)(C)C)C[C@H]2Cc3ccc(CCCO)nc3N21
Reaction #12016
compound
Ausbeute 50.5%DOI: 10.6084/m9.figshare.5104873.v1
NCCCc1ccccn1
Reaction #51195
title product
Ausbeute 97.9%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)[Si](OC(=CCl)c1ccccn1)(C(C)C)C(C)C
Reaction #51980
2-{2-chloro-1-[(triisopropylsilyl)oxy]ethenyl}pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(CCl)c1ccccn1
Reaction #51981
title compound
Ausbeute 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCCc1ccccn1)C(c1cccs1)c1cccs1
Reaction #52575
Dithiophenylacetic Acid, 2-(2-pyridinyl)ethyl Ester
DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1ccccc1.C=Cc1ccccc1C=C.C=Cc1ccccn1
Reaction #54211
white solids
Ausbeute 232.3%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #59638
poly(2-vinylpyridine)
DOI: 10.6084/m9.figshare.5104873.v1
C(=C\c1cccc2c3c([nH]c12)C1CCN(CC1)C3)/c1ccccn1
Reaction #66072
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C=Cc1ncccc1C#N
Reaction #75340
N,N-dimethyl-2-(3-cyano-2-pyridyl) ethenamine
DOI: 10.6084/m9.figshare.5104873.v1
Oc1ccc2cnccc2n1
Reaction #75342
hydroxy-1,6-naphthyridine
Ausbeute 56.0%DOI: 10.6084/m9.figshare.5104873.v1
C(=Cc1ccccn1)c1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #76794
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
C(=Cc1ccccn1)c1cnc2c(c1)C[C@@]1(CN3CCC1CC3)O2
Reaction #77892
title compound
Ausbeute 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cccc(COC(=O)N[C@H](C(=O)N[C@@H](Cc2ccccc2)[C@@H](O)C[C@@H](Cc2ccccc2)NC(=O)OCc2ccco2)C(C)C)n1
Reaction #81117
desired compound
Ausbeute 96.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C(OCC)c1ncccc1C(=O)OCC
Reaction #88890
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cccnc1C(C)=O
Reaction #88891
title compound
Ausbeute 63.6%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCNC(=O)c1ccc(/C(=C\C2CCCC2)c2ccc(C3CC3)c(=O)[nH]2)cc1
Reaction #157778
title compound
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1
C=C1CCOC1=O.C=Cc1ccccn1
Reaction #171137
α-methylene-γ-butyrolactone 2-vinylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOCCn1c(CN2CCN(CCc3ccccn3)CC2)nc2cccnc21
Reaction #172997
DOI: 10.1039/C8SC04228D
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