vinyl tributyltin

C=Cc1cccc(CC(=O)OCC)c1
Reaction #3067
ethyl 3-vinylphenylacetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCc1cccc(C(=O)OC)c1
Reaction #5070
Methyl 3-ethylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #5641
title compound
Yield 88.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
C=Cc1cc(-c2ccc(O)cc2)nc2ccc(O)cc12
Reaction #7336
2-(4-Hydroxyphenyl)-4-vinylquinolin-6-ol
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=Cc1cc(-c2ccc(O)c(F)c2)nc2c(Cl)cc(O)cc12
Reaction #7353
8-Chloro-2-(3-fluoro-4-hydroxyphenyl)-4-vinylquinolin-6-ol
Yield 84.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
C=Cc1cccc(OC2=CC(=O)N([C@@H](CC(C)C)C(=O)OCC)C2)c1F
Reaction #47442
(S)-2-[4-(2-fluoro-3-vinyl-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoic acid ethyl ester
Yield 73.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=Cc1ccc(N)c2c1CNC2=O
Reaction #49464
7-amino-4-vinylisoindolinone
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
C=Cc1cccc(C(CN2CCN(C(=O)OC(C)(C)C)CC2)C2(O)CCCCC2)c1
Reaction #57099
tert-butyl 4-[2-(1-hydroxycyclohexyl)-2-(3-vinylphenyl)ethyl]piperazine-1-carboxylate
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=Cc1cccc2oc(C(=O)OCC)c(C)c12
Reaction #57598
3-methyl-4-vinylbenzofuran-2-carboxylic acid ethyl ester
Yield 75.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=Cc1nn(C(c2ccccc2)(c2ccccc2)c2ccccc2)c2c(F)cc(C#N)cc12
Reaction #62302
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
C=CC1=C(C(=O)OC(c2ccccc2)c2ccccc2)N2C(=O)C(NC(=O)COc3ccccc3)[C@H]2SC1
Reaction #65627
title compound
Yield 88.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
C=Cc1ncn(-c2ccc(Nc3nccc(-c4cccc(N5CCOCC5)c4)n3)cc2)n1
Reaction #69019
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=Cc1ccc2c(c1)N(C)CCN=C2C=Cc1ccc(Cl)c(Cl)c1.Cl.Cl
Reaction #76618
(E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1-methyl-8-vinyl-1H-1,4-benzodiazepine dihydrochloride
Yield 52.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
C=Cc1c(OC)cnnc1-c1cccc(C(F)(F)F)c1
Reaction #81055
4-ethenyl-5-methoxy-3-[3-(trifluoromethyl)phenyl]pyridazine
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=Cc1c(OC)cnnc1-c1cccc(C(F)(F)F)c1
Reaction #82931
4-ethenyl-5-methoxy-3-[3-(trifluoromethyl) phenyl]pyridazine
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
C=Cc1ccc(C(=O)O)c(Cl)c1
Reaction #88834
2-chloro-4-vinylbenzoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C=Cc1cccnc1C(=O)OC
Reaction #155469
methyl 3-vinylpicolinate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=Cc1c(F)cc2ncccc2c1F
Reaction #156320
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=Cc1cnc(N)cc1F
Reaction #156328
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
C=Cc1cnc2ccc(Cc3cnc4ccc(-c5cnn(C)c5)nn34)cn12
Reaction #156478
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
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