tris(dibenzylideneacetone) dipalladium(0)

Cc1cc(Nc2cncc(Sc3ccc(NC(=O)C4CC4)cc3)n2)[nH]n1
Reaction #44476
title compound
المردود 6.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1cccc(-c2cncc(Nc3ccc(N4CCOCC4)cc3)n2)c1
Reaction #44545
pure title compound
المردود 29.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(=O)Nc1cccc(-c2cncc(Nc3cccc(OCCNC(=O)OC(C)(C)C)c3)n2)c1
Reaction #44549
title compound
المردود 43.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(Cc1ccccc1Sc1ccc2c(ccn2C(=O)OC(C)(C)C)c1)C(=O)OC(C)(C)C
Reaction #44896
5-{2-[(tert-butoxycarbonyl-methyl-amino)-methyl]-phenylsulfanyl}-indole-1-carboxylic acid tert-butyl ester
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CN(Cc1ccccc1Sc1ccc2c(ccn2C(=O)OC(C)(C)C)c1)C(=O)OC(C)(C)C
Reaction #44920
5-{2-[(tert-butoxycarbonyl-methyl-amino)-methyl]-phenylsulfanyl}-indole-1-carboxylic acid tert-butyl ester
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC(C)(C)OC(=O)Nc1cnc(Cl)c(F)c1
Reaction #88512
title compound
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
c1ccc(-c2ccc(-c3cccc(-n4c5ccccc5c5ccc6c7ccccc7[nH]c6c54)c3)cc2)cc1
Reaction #92813
N-(1,1′:4′,1″-terphenyl-3-yl)indolo[2,3-a]carbazole
المردود 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
—
Reaction #157811
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
—
Reaction #161637
material
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CCOC(=O)C1CCN(c2ccc(Cl)c(-c3nc4ccncc4[nH]3)c2)CC1
Reaction #164273
mixture
المردود 126.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)Nc1cc(F)ccn1
Reaction #166429
tert-butyl 4-fluoropyridin-2-ylcarbamate
المردود 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
CC(C)(C)OC(=O)Nc1cc(F)ccn1
Reaction #166601
tert-butyl 4-fluoropyridin-2-ylcarbamate
المردود 70.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=S(=O)(Nc1ccc(Cl)cc1-n1nnc2ncccc21)c1ccc(N2CCOCC2)c(F)c1
Reaction #305388
desired product
المردود 44.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)(C)OC(=O)N1CCN(c2nccnc2-c2ccc(Cl)cc2)CC1
Reaction #307605
3′-(4-chloro-phenyl)-2,3,5,6-tetrahydro-[1,2′]bipyrazinyl-4-carboxylic acid t-butyl ester
المردود 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(=O)OC[C@H]1O[C@@H](c2ccc(C)c(Cc3ccc(-c4ccc(F)nc4)s3)c2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #308184
1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-3-(5-(6-fluoro-3-pyridyl)-2-thienylmethyl)-4-methylbenzene
المردود 19.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(=O)OC[C@H]1O[C@@H](c2ccc(C)c(Cc3ccc(-c4cncnc4)s3)c2)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O
Reaction #308188
1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-4-methyl-3-(5-(5-pyrimidinyl)-2-thienylmethyl)benzene
المردود 41.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COc1ccc(CNc2ccc3ccc4ncc(Cl)cc4c(=O)c3c2)c(OC)c1
Reaction #309441
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CN(Cc1ccccc1Sc1ccc2c(ccn2C(=O)OC(C)(C)C)c1)C(=O)OC(C)(C)C
Reaction #317031
5-{2-[(tert-butoxycarbonyl-methyl-amino)-methyl]-phenylsulfanyl}-indole-1-carboxylic acid tert-butyl ester
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
COc1cccc(Nc2c(C(N)=O)cnc3ccc(Sc4ccc(O[Si](C)(C)C(C)(C)C)cc4)cc23)c1
Reaction #318035
title compound
المردود 46.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCOC(=O)CCCCCCc1cccc(C(N)(Cc2ccccc2)c2cc(F)cc(C(F)(F)F)c2)c1
Reaction #325923
ethyl 7-(3-(1-amino-1-(3-fluoro-5-(trifluoromethyl)phenyl)-2-phenylethyl)phenyl)heptanoate
المردود 54.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
الصفحة 1التالي