palladium on carbon

Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #111
المردود 81.0%750 AstraZeneca ELN dataset
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #112
المردود 88.0%750 AstraZeneca ELN dataset
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #113
المردود 73.0%750 AstraZeneca ELN dataset
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #114
المردود 79.0%750 AstraZeneca ELN dataset
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #115
المردود 85.0%750 AstraZeneca ELN dataset
Cc1ncc(-c2nc(Nc3ccc(CN4CCOCC4)cc3F)ncc2F)n1C1CCOCC1
Reaction #116
المردود 85.0%750 AstraZeneca ELN dataset
Cc1c(N)ccc2c1C(=O)NS2(=O)=O
Reaction #905
4-Methyl-5-aminosaccharin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N=C(NC(=O)OCc1ccccc1)N1CCC(CCN)CC1
Reaction #957
4-Aminoethyl-1-benzyloxycarbonylamidino piperidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
c1ccc(CCCC2OCCCO2)nc1
Reaction #982
acetal
المردود 92.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC#Cc1cncc(C2CCCN2C)c1
Reaction #1137
5-propynyl-3-(1-methyl-2-pyrrolidinyl)pyridine
المردود 312.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
C#CC(C)(O)Cc1cncc(C2CCCN2C(=O)OC(C)(C)C)c1
Reaction #1138
5-(2-hydroxy-2-methyl-3-butynyl)-3-(1-tert-butyloxycarbonyl-2-pyrrolidinyl)pyridine
المردود 76.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
Nc1ccccc1C(=O)c1ccc(F)cc1
Reaction #1244
2-amino-4'-fluorobenzophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCOc1cnc(-c2ccc(CCCCO)cc2)nc1
Reaction #1255
2-(4-(4-hydroxybutyl)-phenyl)-5-decyloxypyrimidine
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(Cc1ccccc1)C(=O)O
Reaction #1292
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)c1cccc(N)c1C
Reaction #1381
methyl 2-methyl-3-aminobenzoate
المردود 101.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(C)(C)C=NC1CCNC1
Reaction #1409
3-(2,2-dimethyl-propylidene-amino)-pyrrolidine
المردود 58.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC(Cc1ccccc1)C(=O)O
Reaction #1428
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CC1(C)CCC(=O)c2cc(N)ccc21
Reaction #1480
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C(O)c1ccc2c(c1)CCC(O)C2
Reaction #1506
5,6,7,8-tetrahydro-6-hydroxynaphthalene-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CCCCCCCCCCOc1ccc(C(=O)OC2CCc3cc(C(=O)O)ccc3C2)cc1
Reaction #1511
6-(4'-decyloxybenzoyloxy)-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid
المردود 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
الصفحة 1التالي