bis(tri-t-butylphosphine)palladium(0)

COC(=O)[C@H](Cc1ccccc1)n1cc(-c2cccc3ccccc23)cc(NC(=O)c2ccc(C(F)(F)F)cc2)c1=O
Reaction #7903
title compound
Ausbeute 81.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(SCC=C(c2ccc(-c3ccccc3)cc2)c2ccc(-c3ccccc3)cc2)ccc1OCC(=O)O
Reaction #9436
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(SCC=C(c2ccc(-c3cccc(C(F)(F)F)c3)cc2)c2ccc(-c3cccc(C(F)(F)F)c3)cc2)ccc1OCC(=O)O
Reaction #9438
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
Cc1cc(SCC=C(c2ccc(-c3ccc(-c4ccccc4)cc3)cc2)c2ccc(-c3ccc(-c4ccccc4)cc3)cc2)ccc1OCC(=O)O
Reaction #9439
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
c1ccc2cc3ccccc3cc2c1
Reaction #9799
Anthracene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(OC)c(-c2cnn(C(=O)OC(C)(C)C)c2)cc1C=O
Reaction #10791
4-(5-formyl-2,4-dimethoxy-phenyl)-pyrazole-1-carboxylic acid tert-butyl ester
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=Cc1cccc(C2CC=CO2)c1
Reaction #10843
3-(2,3-dihydro-furan-2-yl)-benzaldehyde
Ausbeute 40.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(OC)c(C2C=CCO2)cc1C=O
Reaction #10845
5-(2,5-dihydro-furan-2-yl)-2,4-dimethoxy-benzaldehyde
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCOC(=O)/C=C/c1cc(CO[Si](C)(C)C(C)(C)C)cc(OC)n1
Reaction #43626
desired product
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(Cn2cc(-c3cccc(CO)c3)c(C(=O)Nc3ccccc3)n2)cc1
Reaction #48601
4-(3-hydroxymethyl-phenyl)-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide
Ausbeute 131.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)/C=C/c1cc(OC)cc2c1ccc(=O)n2CCN1CCC(N(Cc2ccc3c(c2)OCCO3)C(=O)OC(C)(C)C)CC1
Reaction #68057
ethyl (2E)-3-(1-(2-(4-((tert-butoxycarbonyl)(2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-2-oxo-1,2-dihydroquinolin-5-yl)acrylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CSc1ncc(C#N)c(-c2cn(S(=O)(=O)c3ccc(C)cc3)c3ncc(C)cc23)n1
Reaction #69149
title compound
Ausbeute 87.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COCc1cc(OC)c(-c2c(OC)sc3c(NC(=O)OC(C)(C)C)c(OC)nn23)c(OC)c1
Reaction #69551
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCc1sc2c(NC(=O)OC(C)(C)C)c(COC)nn2c1-c1c(OC)cc(COC)cc1OC
Reaction #69552
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CCCN(c1ccccn1)c1c(OC)nn2c(-c3c(OC)cc(COC)cc3OC)csc12
Reaction #69559
title compound
Ausbeute 21.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C=C(C)c1cc(C(=O)N2Cc3ccc(-c4ccc(N5CCN(C(=O)OC(C)(C)C)CC5)cc4)cc3C2)c(OCc2ccccc2)cc1OCc1ccccc1
Reaction #69721
4-{4-[2-(2,4-bis-benzyloxy-5-isopropenyl-benzoyl)-2,3-dihydro-1H-isoindol-5-yl]-phenyl}piperazine-1-carboxylic acid tert-butyl ester
Ausbeute 26.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CSc1nccc(-n2ccc3c(N4CCC(S(C)(=O)=O)CC4)cccc32)n1
Reaction #70244
desired compound
Ausbeute 43.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccc(CN2C(=O)c3c(C=CS(C)(=O)=O)ccc(N4CCN([C@H](C)c5ccccc5)CC4)c3C2=O)cc1OC
Reaction #70603
Compound 62
Ausbeute 19.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccccc1-c1cc(C)cc(/C(C)=N/c2c(C(C)C)cccc2C(C)C)c1O
Reaction #73707
yellowish solid
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
COc1ccccc1-c1cc(C)cc(/C(=N/c2c(C(C)C)cccc2C(C)C)c2ccccc2)c1O
Reaction #73712
yellowish solid
Ausbeute 26.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
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