tetrakis(triphenylphosphine) palladium(0)

CC(C)(C)OC(=O)N1CCN(c2cccs2)CC1
Reaction #398
Ausbeute 0.0%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)N[C@@H]1CCC[C@H](C(=O)Nc2cc(-c3cnn4c3CCCCC4)c(F)cn2)C1
Reaction #613
Ausbeute 72.4%750 AstraZeneca ELN dataset
CC1(C)Cc2ncc(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)n2C1
Reaction #622
Ausbeute 80.0%750 AstraZeneca ELN dataset
CC1(C)CCn2ncc(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)c2C1
Reaction #661
Ausbeute 52.8%750 AstraZeneca ELN dataset
CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #663
Ausbeute 35.1%750 AstraZeneca ELN dataset
CC1(C)Cc2c(-c3cc(NC(=O)[C@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #664
Ausbeute 53.6%750 AstraZeneca ELN dataset
CC(C)(C)OC(=O)N[C@@H]1CCC[C@H](C(=O)Nc2cc(-c3cnn4c3CCCC4)c(F)cn2)C1
Reaction #694
Ausbeute 37.4%750 AstraZeneca ELN dataset
CC1(C)Cc2c(-c3cc(NC(=O)[C@@H]4CCC[C@@H](NC(=O)OC(C)(C)C)C4)ncc3F)cnn2C1
Reaction #743
Ausbeute 84.4%750 AstraZeneca ELN dataset
CC(C)(C)[Si](C)(C)Oc1ccc(C(=O)Oc2ccc(C(=O)O)cn2)cc1C12CC3CC(CC(C3)C1)C2
Reaction #1739
6-[3-adamantan-1-yl-4-(tert-butyl-dimethyl-silanyloxy)-benzoyloxy]-nicotinic acid
Ausbeute 22.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCc1cnc(-c2ccc3c(c2)CC(CCCCCCCC)O3)nc1
Reaction #3161
5-(5-decylpyrimidine-2-yl)-2-octylcoumaran
Ausbeute 23.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCc1cnc(-c2ccc(-c3ccc4c(c3)CC(CCCCCCCC)O4)cc2)nc1
Reaction #3162
5-[4-(5-decylpyrimidine-2-yl)phenyl]-2-octylcoumaran
Ausbeute 66.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Brc1cncc(-c2ccccc2)c1
Reaction #3427
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Cc1csc(-c2cc(C3=C(c4cc(-c5cc(C)cs5)sc4C)C(F)(F)C(F)(F)C3(F)F)c(C)s2)c1
Reaction #3785
1,2-bis[2-methyl-5-(4-methyl-2-thienyl)-3-thienyl]hexafluorocyclopentene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
FC1(F)C=CC(F)(F)C1(F)F
Reaction #3786
hexafluorocyclopentene
Ausbeute 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCC#Cc1ccc(OC)cc1CCN(C)C.Cl
Reaction #4382
2-(1-hexynyl)-5-methoxy-N,N-dimethylbenzeneethanamine hydrochloride
Ausbeute 27.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_02
CC(=O)NCC1OC(=O)N2c3ccc(-c4ccccc4)cc3CC12
Reaction #6332
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1Cc2cc(-c3cccc(Cl)c3)ccc2N1
Reaction #7089
title compound
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC1(C)C(=O)Nc2ccc(-c3ccc(F)c(Cl)c3)cc21
Reaction #7104
title compound
Ausbeute 30.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(CC(=O)Nc2cccc(C3CCCCC3)c2)ccc1O
Reaction #7157
desired compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(Cc1c[nH]c2c(-c3ccc(C(F)(F)F)cc3)cccc12)NC(=O)OC(C)(C)C
Reaction #8188
{1,1-dimethyl-2-[7-(4-trifluoromethyl-phenyl)-1 H-indol-3-yl]-ethyl}-carbamic acid tert-butyl ester
Ausbeute 93.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
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