مشارك في 169 تفاعل

10269

CC(CC(=O)O)C(=O)c1ccc(-n2ccc(=O)cc2)cc1
Reaction #5907
3-[4-(4-oxo-1,4-dihydropyridin-1-yl)benzoyl]butanoic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1c2ccccc2C(=O)N1COc1ccncc1
Reaction #6224
desired compound
المردود 21.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1c2ccccc2C(=O)N1CCCOc1ccncc1
Reaction #6234
desired compound
المردود 16.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1c2ccccc2C(=O)N1CCCCOc1ccncc1
Reaction #6235
desired compound
المردود 17.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
O=C1c2ccccc2C(=O)N1CCOc1ccncc1
Reaction #6244
desired compound
المردود 3.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
COc1cc(Nc2cncc(Oc3ccncc3)n2)cc(OC)c1OC
Reaction #44586
title compound
المردود 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=c1ccn(-c2ccc([N+](=O)[O-])cc2)cc1
Reaction #46808
1-(4-Nitro-phenyl)-1H-pyridin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CC#COc1ccncc1
Reaction #55319
4-(propynyloxy)pyridine
المردود 3.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1980_09
COC(=O)[C@H]1C[C@H](Oc2ccncc2)CN(C(=O)OC(C)(C)C)[C@@H]1C(=O)N1CC=C(c2ccccc2)CC1
Reaction #89724
1-tert-butyl 3-methyl(2S,3S,5S)-2-[(4-phenyl-3,6-dihydropyridin-1(2H)-yl)carbonyl]-5-(pyridin-4-yloxy)piperidine-1,3-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
COC(=O)[C@H]1C[C@H](Oc2ccncc2)CC[C@@H]1C(=O)OC(C)(C)C
Reaction #89776
1-tert-butyl 2-methyl(1S,2S,4R)-4-(pyridin-4-yloxy)cyclohexane-1,2-dicarboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
C[C@H](F)COc1ccncc1
Reaction #156305
4-{[(2S)-2-fluoropropyl]oxy}pyridine
المردود 89.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCOc2ccncc2)CC1OC
Reaction #178341
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2C(=O)N1COc1ccncc1
Reaction #193555
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1c2ccccc2C(=O)N1CCCCOc1ccncc1
Reaction #205480
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(NC1CCC(Oc2ccncc2)CC1)C1CCCN(S(=O)(=O)c2ccccc2)C1
Reaction #211692
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC12CCC(O)CC1CCC1C2CCC2(C)C(C(=O)COc3ccncc3)CCC12
Reaction #212328
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NC1CCC(Oc2ccncc2)CC1
Reaction #222542
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1OC2(CCN(C(=O)C3(c4ccc(N5CCC(Oc6ccncc6)CC5)nc4)CC3)C2)c2ccccc21
Reaction #231976
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCOC(=O)CCCOc1ccncc1
Reaction #251476
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
O=C1c2ccccc2C(=O)N1CCCOc1ccncc1
Reaction #296838
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
الصفحة 1التالي